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- Bbc6effa54da6b0ae4ba3348b81f3db4a NCIT_P378 "NCI" @default.
- Bbc6effa54da6b0ae4ba3348b81f3db4a type Axiom @default.
- Bbc6effa54da6b0ae4ba3348b81f3db4a annotatedProperty IAO_0000115 @default.
- Bbc6effa54da6b0ae4ba3348b81f3db4a annotatedSource NCIT_C1563 @default.
- Bbc6effa54da6b0ae4ba3348b81f3db4a 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.