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ClH/c1-20(2)27(19-28
HIV-1 Nef-IN-1
Smiles: CCCCCCCCCCCC(O)=O
11-8+/t14-
2-Phenyl-2-(1-piperidinyl)propane 0259 ClH/c1-20(2)27(19-28KI: 11 microM for 7 (benzyloxy)resorufin O dealkylation activity of liver microsomes obtained from phenobarbital induced rats 2 Phenyl 2 (1 piperidinyl)propane is a mechanism based inactivator of human cytochrome P450 (CYP) 2B6. The use of selective chemical inhibitors of human cytochrome P450 enzymes is a powerful method by which the relative contributions of different human P450 enzymes to the drug metabolism can be obtained. However, the
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