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Physician Data Query
Preferred Name | dexverapamil | |
Synonyms |
R-Verapamil Hydrochloride R verapamil R-verapamil |
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Definitions |
The R-enantiomer of the calcium channel blocker verapamil. Dexverapamil competitively inhibits the multidrug resistance efflux pump P-glycoprotein (MDR-1), thereby potentially increasing the effectiveness of a wide range of antineoplastic drugs which are inactivated by MDR-1 mechanisms. This agent exhibits decreased calcium antagonistic activity and toxicity compared to racemic verapamil. Check for "https://www.cancer.gov/about-cancer/treatment/clinical-trials/intervention/C1563" active clinical trials using this agent. ("http://ncit.nci.nih.gov/ncitbrowser/ConceptReport.jsp?dictionary=NCI%20Thesaurus&code=C1563" NCI Thesaurus) |
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ID |
http://purl.bioontology.org/ontology/PDQ/CDR0000041269 |
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altLabel |
R-Verapamil Hydrochloride R verapamil R-verapamil
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Component of |
http://purl.bioontology.org/ontology/PDQ/CDR0000041740 http://purl.bioontology.org/ontology/PDQ/CDR0000042150 http://purl.bioontology.org/ontology/PDQ/CDR0000041272 http://purl.bioontology.org/ontology/PDQ/CDR0000041271 |
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cui |
C0280858 C1527029
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Date last modified |
2006-12-12
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definition |
The R-enantiomer of the calcium channel blocker verapamil. Dexverapamil competitively inhibits the multidrug resistance efflux pump P-glycoprotein (MDR-1), thereby potentially increasing the effectiveness of a wide range of antineoplastic drugs which are inactivated by MDR-1 mechanisms. This agent exhibits decreased calcium antagonistic activity and toxicity compared to racemic verapamil. Check for "https://www.cancer.gov/about-cancer/treatment/clinical-trials/intervention/C1563" active clinical trials using this agent. ("http://ncit.nci.nih.gov/ncitbrowser/ConceptReport.jsp?dictionary=NCI%20Thesaurus&code=C1563" NCI Thesaurus)
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IND Code |
34790
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Legacy PDQ ID |
4342
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NCI ID |
C1563
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notation |
CDR0000041269
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ORIG STY |
Drug/agent
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prefLabel |
dexverapamil
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tui |
T109 T121
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