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IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
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IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). 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IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally related to CBD on CYP1A1 activity were examined with recombinant human CYP1A1 in order to characterize the structural requirements for potent inactivation by CBD. When preincubated in the presence of NADPH for 20min, olivetol, which corresponds to the pentylresorcinol moiety of CBD, enhanced the inhibition of the 7-ethoxyresorufin O-deethylase activity of CYP1A1. In contrast, d-limonene, which corresponds to the terpene moiety of CBD, failed to inhibit CYP1A1 activity in a metabolism-dependent manner. Pentylbenzene, which lacks two free phenolic hydroxyl groups, also did not enhance CYP1A1 inhibition. On the other hand, preincubation of the CBD-2'-monomethyl ether (CBDM) and CBD-2',6'-dimethyl ether (CBDD) enhanced the inhibition of CYP1A1 activity. 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IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally related to CBD on CYP1A1 activity were examined with recombinant human CYP1A1 in order to characterize the structural requirements for potent inactivation by CBD. When preincubated in the presence of NADPH for 20min, olivetol, which corresponds to the pentylresorcinol moiety of CBD, enhanced the inhibition of the 7-ethoxyresorufin O-deethylase activity of CYP1A1. In contrast, d-limonene, which corresponds to the terpene moiety of CBD, failed to inhibit CYP1A1 activity in a metabolism-dependent manner. Pentylbenzene, which lacks two free phenolic hydroxyl groups, also did not enhance CYP1A1 inhibition. On the other hand, preincubation of the CBD-2'-monomethyl ether (CBDM) and CBD-2',6'-dimethyl ether (CBDD) enhanced the inhibition of CYP1A1 activity. Inhibition by cannabidivarin (CBDV), which possessed a propyl side chain, was strongly potentiated by its preincubation. Orcinol, which has a methyl group, augmented CYP1A1 inhibition, whereas its derivative without an alkyl side chain, resorcinol, did not exhibit any metabolism-dependent inhibition. The preincubation of CBD-hydroxyquinone did not markedly enhance CYP1A1 inhibition. We further confirmed that olivetol, CBDM, CBDD, CBDV, and orcinol, as well as CBD (kinact=0.215min(-1)), inactivated CYP1A1 activity; their kinact values were 0.154, 0.0638, 0.0643, 0.226, and 0.0353min(-1), respectively. These results suggest that the methylresorcinol structure in CBD may have structurally important roles in the inactivation of CYP1A1.","study.pubmedId":24667653,"study.embaseId":null,"study.croIdentifier":"Hokuriku University","study.croInformation":"Hokuriku University","study.dateStart":null,"study.dateEnd":null,"study.internalComment":null,"study.status":"published","study.compoundId":null,"study.naturalProductUid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProductSampleId":null,"study.studySourceTypeId":1,"study.naturalProduct.uid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProduct.binomial":"Cannabis 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IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally related to CBD on CYP1A1 activity were examined with recombinant human CYP1A1 in order to characterize the structural requirements for potent inactivation by CBD. When preincubated in the presence of NADPH for 20min, olivetol, which corresponds to the pentylresorcinol moiety of CBD, enhanced the inhibition of the 7-ethoxyresorufin O-deethylase activity of CYP1A1. In contrast, d-limonene, which corresponds to the terpene moiety of CBD, failed to inhibit CYP1A1 activity in a metabolism-dependent manner. Pentylbenzene, which lacks two free phenolic hydroxyl groups, also did not enhance CYP1A1 inhibition. On the other hand, preincubation of the CBD-2'-monomethyl ether (CBDM) and CBD-2',6'-dimethyl ether (CBDD) enhanced the inhibition of CYP1A1 activity. Inhibition by cannabidivarin (CBDV), which possessed a propyl side chain, was strongly potentiated by its preincubation. Orcinol, which has a methyl group, augmented CYP1A1 inhibition, whereas its derivative without an alkyl side chain, resorcinol, did not exhibit any metabolism-dependent inhibition. The preincubation of CBD-hydroxyquinone did not markedly enhance CYP1A1 inhibition. We further confirmed that olivetol, CBDM, CBDD, CBDV, and orcinol, as well as CBD (kinact=0.215min(-1)), inactivated CYP1A1 activity; their kinact values were 0.154, 0.0638, 0.0643, 0.226, and 0.0353min(-1), respectively. 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µL","experimentAnswers.answerId":null,"experimentAnswers.experimentId":314,"experimentAnswers.questionId":20,"experimentAnswers.question.id":20,"experimentAnswers.question.text":"Precipitant pre-incubation volume","experimentAnswers.question.required":false,"experimentAnswers.question.maxAnswers":null,"experimentAnswers.question.type":"STRING","experimentAnswers.question.conceptId":null,"experimentAnswers.question.answers.id":null,"experimentAnswers.question.answers.text":null,"experimentAnswers.question.answers.sortOrder":null,"experimentAnswers.question.answers.conceptId":null,"experimentAnswers.question.answers.questionId":null,"experimentAnswers.answer.id":null,"experimentAnswers.answer.text":null,"experimentAnswers.answer.sortOrder":null,"experimentAnswers.answer.conceptId":null,"experimentAnswers.answer.questionId":null},{"id":314,"uid":"NPDI-DqfMEw","name":"Cannbidiol-2'-monomethyl ether","overallEffect":1,"isControlData":false,"isIc50Shift":false,"croCutoff":"Not specified","croIdentifier":null,"comment":null,"experimentalConditionsComment":null,"resultsComment":"%inhibition estimated from Figure 2.
IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally related to CBD on CYP1A1 activity were examined with recombinant human CYP1A1 in order to characterize the structural requirements for potent inactivation by CBD. When preincubated in the presence of NADPH for 20min, olivetol, which corresponds to the pentylresorcinol moiety of CBD, enhanced the inhibition of the 7-ethoxyresorufin O-deethylase activity of CYP1A1. In contrast, d-limonene, which corresponds to the terpene moiety of CBD, failed to inhibit CYP1A1 activity in a metabolism-dependent manner. Pentylbenzene, which lacks two free phenolic hydroxyl groups, also did not enhance CYP1A1 inhibition. On the other hand, preincubation of the CBD-2'-monomethyl ether (CBDM) and CBD-2',6'-dimethyl ether (CBDD) enhanced the inhibition of CYP1A1 activity. Inhibition by cannabidivarin (CBDV), which possessed a propyl side chain, was strongly potentiated by its preincubation. Orcinol, which has a methyl group, augmented CYP1A1 inhibition, whereas its derivative without an alkyl side chain, resorcinol, did not exhibit any metabolism-dependent inhibition. The preincubation of CBD-hydroxyquinone did not markedly enhance CYP1A1 inhibition. We further confirmed that olivetol, CBDM, CBDD, CBDV, and orcinol, as well as CBD (kinact=0.215min(-1)), inactivated CYP1A1 activity; their kinact values were 0.154, 0.0638, 0.0643, 0.226, and 0.0353min(-1), respectively. These results suggest that the methylresorcinol structure in CBD may have structurally important roles in the inactivation of CYP1A1.","study.pubmedId":24667653,"study.embaseId":null,"study.croIdentifier":"Hokuriku University","study.croInformation":"Hokuriku University","study.dateStart":null,"study.dateEnd":null,"study.internalComment":null,"study.status":"published","study.compoundId":null,"study.naturalProductUid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProductSampleId":null,"study.studySourceTypeId":1,"study.naturalProduct.uid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProduct.binomial":"Cannabis 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IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally related to CBD on CYP1A1 activity were examined with recombinant human CYP1A1 in order to characterize the structural requirements for potent inactivation by CBD. When preincubated in the presence of NADPH for 20min, olivetol, which corresponds to the pentylresorcinol moiety of CBD, enhanced the inhibition of the 7-ethoxyresorufin O-deethylase activity of CYP1A1. In contrast, d-limonene, which corresponds to the terpene moiety of CBD, failed to inhibit CYP1A1 activity in a metabolism-dependent manner. Pentylbenzene, which lacks two free phenolic hydroxyl groups, also did not enhance CYP1A1 inhibition. On the other hand, preincubation of the CBD-2'-monomethyl ether (CBDM) and CBD-2',6'-dimethyl ether (CBDD) enhanced the inhibition of CYP1A1 activity. 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pre-incubation condition","experimentAnswers.question.required":false,"experimentAnswers.question.maxAnswers":1,"experimentAnswers.question.type":null,"experimentAnswers.question.conceptId":null,"experimentAnswers.question.answers.id":25,"experimentAnswers.question.answers.text":"No NADPH with precipitant","experimentAnswers.question.answers.sortOrder":null,"experimentAnswers.question.answers.conceptId":null,"experimentAnswers.question.answers.questionId":22,"experimentAnswers.answer.id":23,"experimentAnswers.answer.text":"NADPH with precipitant","experimentAnswers.answer.sortOrder":null,"experimentAnswers.answer.conceptId":null,"experimentAnswers.answer.questionId":22},{"id":314,"uid":"NPDI-DqfMEw","name":"Cannbidiol-2'-monomethyl ether","overallEffect":1,"isControlData":false,"isIc50Shift":false,"croCutoff":"Not specified","croIdentifier":null,"comment":null,"experimentalConditionsComment":null,"resultsComment":"%inhibition estimated from Figure 2.
IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally related to CBD on CYP1A1 activity were examined with recombinant human CYP1A1 in order to characterize the structural requirements for potent inactivation by CBD. When preincubated in the presence of NADPH for 20min, olivetol, which corresponds to the pentylresorcinol moiety of CBD, enhanced the inhibition of the 7-ethoxyresorufin O-deethylase activity of CYP1A1. In contrast, d-limonene, which corresponds to the terpene moiety of CBD, failed to inhibit CYP1A1 activity in a metabolism-dependent manner. Pentylbenzene, which lacks two free phenolic hydroxyl groups, also did not enhance CYP1A1 inhibition. On the other hand, preincubation of the CBD-2'-monomethyl ether (CBDM) and CBD-2',6'-dimethyl ether (CBDD) enhanced the inhibition of CYP1A1 activity. Inhibition by cannabidivarin (CBDV), which possessed a propyl side chain, was strongly potentiated by its preincubation. Orcinol, which has a methyl group, augmented CYP1A1 inhibition, whereas its derivative without an alkyl side chain, resorcinol, did not exhibit any metabolism-dependent inhibition. The preincubation of CBD-hydroxyquinone did not markedly enhance CYP1A1 inhibition. We further confirmed that olivetol, CBDM, CBDD, CBDV, and orcinol, as well as CBD (kinact=0.215min(-1)), inactivated CYP1A1 activity; their kinact values were 0.154, 0.0638, 0.0643, 0.226, and 0.0353min(-1), respectively. These results suggest that the methylresorcinol structure in CBD may have structurally important roles in the inactivation of CYP1A1.","study.pubmedId":24667653,"study.embaseId":null,"study.croIdentifier":"Hokuriku University","study.croInformation":"Hokuriku University","study.dateStart":null,"study.dateEnd":null,"study.internalComment":null,"study.status":"published","study.compoundId":null,"study.naturalProductUid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProductSampleId":null,"study.studySourceTypeId":1,"study.naturalProduct.uid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProduct.binomial":"Cannabis 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IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally related to CBD on CYP1A1 activity were examined with recombinant human CYP1A1 in order to characterize the structural requirements for potent inactivation by CBD. When preincubated in the presence of NADPH for 20min, olivetol, which corresponds to the pentylresorcinol moiety of CBD, enhanced the inhibition of the 7-ethoxyresorufin O-deethylase activity of CYP1A1. In contrast, d-limonene, which corresponds to the terpene moiety of CBD, failed to inhibit CYP1A1 activity in a metabolism-dependent manner. Pentylbenzene, which lacks two free phenolic hydroxyl groups, also did not enhance CYP1A1 inhibition. On the other hand, preincubation of the CBD-2'-monomethyl ether (CBDM) and CBD-2',6'-dimethyl ether (CBDD) enhanced the inhibition of CYP1A1 activity. 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IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally related to CBD on CYP1A1 activity were examined with recombinant human CYP1A1 in order to characterize the structural requirements for potent inactivation by CBD. When preincubated in the presence of NADPH for 20min, olivetol, which corresponds to the pentylresorcinol moiety of CBD, enhanced the inhibition of the 7-ethoxyresorufin O-deethylase activity of CYP1A1. In contrast, d-limonene, which corresponds to the terpene moiety of CBD, failed to inhibit CYP1A1 activity in a metabolism-dependent manner. Pentylbenzene, which lacks two free phenolic hydroxyl groups, also did not enhance CYP1A1 inhibition. On the other hand, preincubation of the CBD-2'-monomethyl ether (CBDM) and CBD-2',6'-dimethyl ether (CBDD) enhanced the inhibition of CYP1A1 activity. Inhibition by cannabidivarin (CBDV), which possessed a propyl side chain, was strongly potentiated by its preincubation. Orcinol, which has a methyl group, augmented CYP1A1 inhibition, whereas its derivative without an alkyl side chain, resorcinol, did not exhibit any metabolism-dependent inhibition. The preincubation of CBD-hydroxyquinone did not markedly enhance CYP1A1 inhibition. We further confirmed that olivetol, CBDM, CBDD, CBDV, and orcinol, as well as CBD (kinact=0.215min(-1)), inactivated CYP1A1 activity; their kinact values were 0.154, 0.0638, 0.0643, 0.226, and 0.0353min(-1), respectively. These results suggest that the methylresorcinol structure in CBD may have structurally important roles in the inactivation of CYP1A1.","study.pubmedId":24667653,"study.embaseId":null,"study.croIdentifier":"Hokuriku University","study.croInformation":"Hokuriku University","study.dateStart":null,"study.dateEnd":null,"study.internalComment":null,"study.status":"published","study.compoundId":null,"study.naturalProductUid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProductSampleId":null,"study.studySourceTypeId":1,"study.naturalProduct.uid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProduct.binomial":"Cannabis 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IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally related to CBD on CYP1A1 activity were examined with recombinant human CYP1A1 in order to characterize the structural requirements for potent inactivation by CBD. When preincubated in the presence of NADPH for 20min, olivetol, which corresponds to the pentylresorcinol moiety of CBD, enhanced the inhibition of the 7-ethoxyresorufin O-deethylase activity of CYP1A1. In contrast, d-limonene, which corresponds to the terpene moiety of CBD, failed to inhibit CYP1A1 activity in a metabolism-dependent manner. Pentylbenzene, which lacks two free phenolic hydroxyl groups, also did not enhance CYP1A1 inhibition. On the other hand, preincubation of the CBD-2'-monomethyl ether (CBDM) and CBD-2',6'-dimethyl ether (CBDD) enhanced the inhibition of CYP1A1 activity. Inhibition by cannabidivarin (CBDV), which possessed a propyl side chain, was strongly potentiated by its preincubation. Orcinol, which has a methyl group, augmented CYP1A1 inhibition, whereas its derivative without an alkyl side chain, resorcinol, did not exhibit any metabolism-dependent inhibition. The preincubation of CBD-hydroxyquinone did not markedly enhance CYP1A1 inhibition. We further confirmed that olivetol, CBDM, CBDD, CBDV, and orcinol, as well as CBD (kinact=0.215min(-1)), inactivated CYP1A1 activity; their kinact values were 0.154, 0.0638, 0.0643, 0.226, and 0.0353min(-1), respectively. These results suggest that the methylresorcinol structure in CBD may have structurally important roles in the inactivation of CYP1A1.","study.pubmedId":24667653,"study.embaseId":null,"study.croIdentifier":"Hokuriku University","study.croInformation":"Hokuriku University","study.dateStart":null,"study.dateEnd":null,"study.internalComment":null,"study.status":"published","study.compoundId":null,"study.naturalProductUid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProductSampleId":null,"study.studySourceTypeId":1,"study.naturalProduct.uid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProduct.binomial":"Cannabis 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IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally related to CBD on CYP1A1 activity were examined with recombinant human CYP1A1 in order to characterize the structural requirements for potent inactivation by CBD. When preincubated in the presence of NADPH for 20min, olivetol, which corresponds to the pentylresorcinol moiety of CBD, enhanced the inhibition of the 7-ethoxyresorufin O-deethylase activity of CYP1A1. In contrast, d-limonene, which corresponds to the terpene moiety of CBD, failed to inhibit CYP1A1 activity in a metabolism-dependent manner. Pentylbenzene, which lacks two free phenolic hydroxyl groups, also did not enhance CYP1A1 inhibition. On the other hand, preincubation of the CBD-2'-monomethyl ether (CBDM) and CBD-2',6'-dimethyl ether (CBDD) enhanced the inhibition of CYP1A1 activity. Inhibition by cannabidivarin (CBDV), which possessed a propyl side chain, was strongly potentiated by its preincubation. Orcinol, which has a methyl group, augmented CYP1A1 inhibition, whereas its derivative without an alkyl side chain, resorcinol, did not exhibit any metabolism-dependent inhibition. The preincubation of CBD-hydroxyquinone did not markedly enhance CYP1A1 inhibition. We further confirmed that olivetol, CBDM, CBDD, CBDV, and orcinol, as well as CBD (kinact=0.215min(-1)), inactivated CYP1A1 activity; their kinact values were 0.154, 0.0638, 0.0643, 0.226, and 0.0353min(-1), respectively. These results suggest that the methylresorcinol structure in CBD may have structurally important roles in the inactivation of CYP1A1.","study.pubmedId":24667653,"study.embaseId":null,"study.croIdentifier":"Hokuriku University","study.croInformation":"Hokuriku University","study.dateStart":null,"study.dateEnd":null,"study.internalComment":null,"study.status":"published","study.compoundId":null,"study.naturalProductUid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProductSampleId":null,"study.studySourceTypeId":1,"study.naturalProduct.uid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProduct.binomial":"Cannabis 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IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally related to CBD on CYP1A1 activity were examined with recombinant human CYP1A1 in order to characterize the structural requirements for potent inactivation by CBD. When preincubated in the presence of NADPH for 20min, olivetol, which corresponds to the pentylresorcinol moiety of CBD, enhanced the inhibition of the 7-ethoxyresorufin O-deethylase activity of CYP1A1. In contrast, d-limonene, which corresponds to the terpene moiety of CBD, failed to inhibit CYP1A1 activity in a metabolism-dependent manner. Pentylbenzene, which lacks two free phenolic hydroxyl groups, also did not enhance CYP1A1 inhibition. On the other hand, preincubation of the CBD-2'-monomethyl ether (CBDM) and CBD-2',6'-dimethyl ether (CBDD) enhanced the inhibition of CYP1A1 activity. Inhibition by cannabidivarin (CBDV), which possessed a propyl side chain, was strongly potentiated by its preincubation. Orcinol, which has a methyl group, augmented CYP1A1 inhibition, whereas its derivative without an alkyl side chain, resorcinol, did not exhibit any metabolism-dependent inhibition. The preincubation of CBD-hydroxyquinone did not markedly enhance CYP1A1 inhibition. We further confirmed that olivetol, CBDM, CBDD, CBDV, and orcinol, as well as CBD (kinact=0.215min(-1)), inactivated CYP1A1 activity; their kinact values were 0.154, 0.0638, 0.0643, 0.226, and 0.0353min(-1), respectively. These results suggest that the methylresorcinol structure in CBD may have structurally important roles in the inactivation of CYP1A1.","study.pubmedId":24667653,"study.embaseId":null,"study.croIdentifier":"Hokuriku University","study.croInformation":"Hokuriku University","study.dateStart":null,"study.dateEnd":null,"study.internalComment":null,"study.status":"published","study.compoundId":null,"study.naturalProductUid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProductSampleId":null,"study.studySourceTypeId":1,"study.naturalProduct.uid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProduct.binomial":"Cannabis 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IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally related to CBD on CYP1A1 activity were examined with recombinant human CYP1A1 in order to characterize the structural requirements for potent inactivation by CBD. When preincubated in the presence of NADPH for 20min, olivetol, which corresponds to the pentylresorcinol moiety of CBD, enhanced the inhibition of the 7-ethoxyresorufin O-deethylase activity of CYP1A1. In contrast, d-limonene, which corresponds to the terpene moiety of CBD, failed to inhibit CYP1A1 activity in a metabolism-dependent manner. Pentylbenzene, which lacks two free phenolic hydroxyl groups, also did not enhance CYP1A1 inhibition. On the other hand, preincubation of the CBD-2'-monomethyl ether (CBDM) and CBD-2',6'-dimethyl ether (CBDD) enhanced the inhibition of CYP1A1 activity. Inhibition by cannabidivarin (CBDV), which possessed a propyl side chain, was strongly potentiated by its preincubation. Orcinol, which has a methyl group, augmented CYP1A1 inhibition, whereas its derivative without an alkyl side chain, resorcinol, did not exhibit any metabolism-dependent inhibition. The preincubation of CBD-hydroxyquinone did not markedly enhance CYP1A1 inhibition. We further confirmed that olivetol, CBDM, CBDD, CBDV, and orcinol, as well as CBD (kinact=0.215min(-1)), inactivated CYP1A1 activity; their kinact values were 0.154, 0.0638, 0.0643, 0.226, and 0.0353min(-1), respectively. These results suggest that the methylresorcinol structure in CBD may have structurally important roles in the inactivation of CYP1A1.","study.pubmedId":24667653,"study.embaseId":null,"study.croIdentifier":"Hokuriku University","study.croInformation":"Hokuriku University","study.dateStart":null,"study.dateEnd":null,"study.internalComment":null,"study.status":"published","study.compoundId":null,"study.naturalProductUid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProductSampleId":null,"study.studySourceTypeId":1,"study.naturalProduct.uid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProduct.binomial":"Cannabis 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IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally related to CBD on CYP1A1 activity were examined with recombinant human CYP1A1 in order to characterize the structural requirements for potent inactivation by CBD. When preincubated in the presence of NADPH for 20min, olivetol, which corresponds to the pentylresorcinol moiety of CBD, enhanced the inhibition of the 7-ethoxyresorufin O-deethylase activity of CYP1A1. In contrast, d-limonene, which corresponds to the terpene moiety of CBD, failed to inhibit CYP1A1 activity in a metabolism-dependent manner. Pentylbenzene, which lacks two free phenolic hydroxyl groups, also did not enhance CYP1A1 inhibition. On the other hand, preincubation of the CBD-2'-monomethyl ether (CBDM) and CBD-2',6'-dimethyl ether (CBDD) enhanced the inhibition of CYP1A1 activity. Inhibition by cannabidivarin (CBDV), which possessed a propyl side chain, was strongly potentiated by its preincubation. Orcinol, which has a methyl group, augmented CYP1A1 inhibition, whereas its derivative without an alkyl side chain, resorcinol, did not exhibit any metabolism-dependent inhibition. The preincubation of CBD-hydroxyquinone did not markedly enhance CYP1A1 inhibition. We further confirmed that olivetol, CBDM, CBDD, CBDV, and orcinol, as well as CBD (kinact=0.215min(-1)), inactivated CYP1A1 activity; their kinact values were 0.154, 0.0638, 0.0643, 0.226, and 0.0353min(-1), respectively. These results suggest that the methylresorcinol structure in CBD may have structurally important roles in the inactivation of CYP1A1.","study.pubmedId":24667653,"study.embaseId":null,"study.croIdentifier":"Hokuriku University","study.croInformation":"Hokuriku University","study.dateStart":null,"study.dateEnd":null,"study.internalComment":null,"study.status":"published","study.compoundId":null,"study.naturalProductUid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProductSampleId":null,"study.studySourceTypeId":1,"study.naturalProduct.uid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProduct.binomial":"Cannabis 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ether","overallEffect":1,"isControlData":false,"isIc50Shift":false,"croCutoff":"Not specified","croIdentifier":null,"comment":null,"experimentalConditionsComment":null,"resultsComment":"%inhibition estimated from Figure 2.
IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally related to CBD on CYP1A1 activity were examined with recombinant human CYP1A1 in order to characterize the structural requirements for potent inactivation by CBD. When preincubated in the presence of NADPH for 20min, olivetol, which corresponds to the pentylresorcinol moiety of CBD, enhanced the inhibition of the 7-ethoxyresorufin O-deethylase activity of CYP1A1. In contrast, d-limonene, which corresponds to the terpene moiety of CBD, failed to inhibit CYP1A1 activity in a metabolism-dependent manner. Pentylbenzene, which lacks two free phenolic hydroxyl groups, also did not enhance CYP1A1 inhibition. On the other hand, preincubation of the CBD-2'-monomethyl ether (CBDM) and CBD-2',6'-dimethyl ether (CBDD) enhanced the inhibition of CYP1A1 activity. Inhibition by cannabidivarin (CBDV), which possessed a propyl side chain, was strongly potentiated by its preincubation. Orcinol, which has a methyl group, augmented CYP1A1 inhibition, whereas its derivative without an alkyl side chain, resorcinol, did not exhibit any metabolism-dependent inhibition. The preincubation of CBD-hydroxyquinone did not markedly enhance CYP1A1 inhibition. We further confirmed that olivetol, CBDM, CBDD, CBDV, and orcinol, as well as CBD (kinact=0.215min(-1)), inactivated CYP1A1 activity; their kinact values were 0.154, 0.0638, 0.0643, 0.226, and 0.0353min(-1), respectively. These results suggest that the methylresorcinol structure in CBD may have structurally important roles in the inactivation of CYP1A1.","study.pubmedId":24667653,"study.embaseId":null,"study.croIdentifier":"Hokuriku University","study.croInformation":"Hokuriku University","study.dateStart":null,"study.dateEnd":null,"study.internalComment":null,"study.status":"published","study.compoundId":null,"study.naturalProductUid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProductSampleId":null,"study.studySourceTypeId":1,"study.naturalProduct.uid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProduct.binomial":"Cannabis 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IC50pre-incubation at 0 min (Table 1).
IC50pre-incubation at 20 min - 1.90
Kinact/KI converted from /min/mmol to /min/μM (table 2).
All other values from Table 2.","internalComment":null,"objectCompoundId":86,"objectMetaboliteCompoundId":87,"precipitantCompoundId":147,"cytochromeB5Id":4,"studyId":79,"experimentTypeId":1,"testSystemId":14,"ic50ShiftExperimentId":null,"controlDataExperimentId":null,"controlDataForExperimentId":null,"naturalProductSampleId":null,"experimentType.id":1,"experimentType.name":"In Vitro Enzyme Inhibition","experimentType.isInVitro":true,"experimentType.isTransporter":false,"experimentType.isEnzyme":true,"experimentType.purl":"http://purl.obolibrary.org/obo/DIDEO_00000058","objectCompound.id":86,"objectCompound.name":"7-ethoxyresorufin","objectCompound.unii":null,"objectCompound.inChIKey":"CRCWUBLTFGOMDD-UHFFFAOYSA-N","objectCompound.publicDescription":null,"objectCompound.internalComment":null,"objectCompound.conceptId":-7999995,"objectCompound.enantiomerOfId":null,"objectCompound.concept.conceptId":-7999995,"objectCompound.concept.conceptName":"7-ethoxyresorufin","objectCompound.concept.domainId":"Metadata","objectCompound.concept.vocabularyId":"CHEBI","objectCompound.concept.conceptClassId":"Domain","objectCompound.concept.standardConcept":"","objectCompound.concept.conceptCode":"34480","objectCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectCompound.concept.invalid_reason":"","precipitantCompound.id":147,"precipitantCompound.name":"cannabidiol-2'-monomethyl ether","precipitantCompound.unii":null,"precipitantCompound.inChIKey":null,"precipitantCompound.publicDescription":null,"precipitantCompound.internalComment":null,"precipitantCompound.conceptId":null,"precipitantCompound.enantiomerOfId":null,"precipitantCompound.concept.conceptId":null,"precipitantCompound.concept.conceptName":null,"precipitantCompound.concept.domainId":null,"precipitantCompound.concept.vocabularyId":null,"precipitantCompound.concept.conceptClassId":null,"precipitantCompound.concept.standardConcept":null,"precipitantCompound.concept.conceptCode":null,"precipitantCompound.concept.validStartDate":null,"precipitantCompound.concept.validEndDate":null,"precipitantCompound.concept.invalid_reason":null,"objectMetaboliteCompound.id":87,"objectMetaboliteCompound.name":"resorufin","objectMetaboliteCompound.unii":null,"objectMetaboliteCompound.inChIKey":null,"objectMetaboliteCompound.publicDescription":null,"objectMetaboliteCompound.internalComment":null,"objectMetaboliteCompound.conceptId":-7999853,"objectMetaboliteCompound.enantiomerOfId":null,"objectMetaboliteCompound.concept.conceptId":-7999853,"objectMetaboliteCompound.concept.conceptName":"resorufin","objectMetaboliteCompound.concept.domainId":"Metadata","objectMetaboliteCompound.concept.vocabularyId":"CHEBI","objectMetaboliteCompound.concept.conceptClassId":"Domain","objectMetaboliteCompound.concept.standardConcept":"","objectMetaboliteCompound.concept.conceptCode":"51602","objectMetaboliteCompound.concept.validStartDate":"2000-01-01T00:00:00.000Z","objectMetaboliteCompound.concept.validEndDate":"2099-02-22T00:00:00.000Z","objectMetaboliteCompound.concept.invalid_reason":"","enzymes.id":32,"enzymes.name":"CYP1A1","enzymes.conceptId":4173297,"enzymes.experiment_enzyme_xref.enzymeId":32,"enzymes.experiment_enzyme_xref.experimentId":314,"transporters.id":null,"transporters.name":null,"transporters.conceptId":null,"transporters.experiment_transporter_xref.experimentId":null,"transporters.experiment_transporter_xref.transporterId":null,"quantifiedMetabolites.id":null,"quantifiedMetabolites.name":null,"quantifiedMetabolites.unii":null,"quantifiedMetabolites.inChIKey":null,"quantifiedMetabolites.publicDescription":null,"quantifiedMetabolites.internalComment":null,"quantifiedMetabolites.conceptId":null,"quantifiedMetabolites.enantiomerOfId":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.com":null,"quantifiedMetabolites.experiment_quantified_metabolite_xref.exp":null,"study.id":79,"study.uid":"NPDI-Z6vbAA","study.name":"Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol","study.napdiIdentifier":"PMID: 24667653","study.overallSummary":"We previously demonstrated that cannabidiol (CBD) was a potent mechanism-based inhibitor of human cytochrome P450 1A1 (CYP1A1). However, the moiety of CBD that contributes to the potent mechanism-based inhibition of human CYP1A1 remains unknown. Thus, the effects of compounds structurally related to CBD on CYP1A1 activity were examined with recombinant human CYP1A1 in order to characterize the structural requirements for potent inactivation by CBD. When preincubated in the presence of NADPH for 20min, olivetol, which corresponds to the pentylresorcinol moiety of CBD, enhanced the inhibition of the 7-ethoxyresorufin O-deethylase activity of CYP1A1. In contrast, d-limonene, which corresponds to the terpene moiety of CBD, failed to inhibit CYP1A1 activity in a metabolism-dependent manner. Pentylbenzene, which lacks two free phenolic hydroxyl groups, also did not enhance CYP1A1 inhibition. On the other hand, preincubation of the CBD-2'-monomethyl ether (CBDM) and CBD-2',6'-dimethyl ether (CBDD) enhanced the inhibition of CYP1A1 activity. Inhibition by cannabidivarin (CBDV), which possessed a propyl side chain, was strongly potentiated by its preincubation. Orcinol, which has a methyl group, augmented CYP1A1 inhibition, whereas its derivative without an alkyl side chain, resorcinol, did not exhibit any metabolism-dependent inhibition. The preincubation of CBD-hydroxyquinone did not markedly enhance CYP1A1 inhibition. We further confirmed that olivetol, CBDM, CBDD, CBDV, and orcinol, as well as CBD (kinact=0.215min(-1)), inactivated CYP1A1 activity; their kinact values were 0.154, 0.0638, 0.0643, 0.226, and 0.0353min(-1), respectively. These results suggest that the methylresorcinol structure in CBD may have structurally important roles in the inactivation of CYP1A1.","study.pubmedId":24667653,"study.embaseId":null,"study.croIdentifier":"Hokuriku University","study.croInformation":"Hokuriku University","study.dateStart":null,"study.dateEnd":null,"study.internalComment":null,"study.status":"published","study.compoundId":null,"study.naturalProductUid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProductSampleId":null,"study.studySourceTypeId":1,"study.naturalProduct.uid":"NP-0162af79-839e-40e2-af47-361c659061e9","study.naturalProduct.binomial":"Cannabis 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