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- Be7f8e763675d00556d6884b6af8470df NCIT_P378 "NCI" @default.
- Be7f8e763675d00556d6884b6af8470df type Axiom @default.
- Be7f8e763675d00556d6884b6af8470df annotatedProperty IAO_0000115 @default.
- Be7f8e763675d00556d6884b6af8470df annotatedSource NCIT_C1563 @default.
- Be7f8e763675d00556d6884b6af8470df annotatedTarget "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. (NCI04)" @default.