Title : Molecular modelling study of pyrrolidine-2,5-dione based aromatase inhibitors and other known inhibitors.

Pub. Date : 1996 Mar

PMID : 8854046






1 Functional Relationships(s)
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1 The study suggests that the "larger" inhibitors (such as the [2"(4"-aminophenyl)alkyl] pyrrolidine-2,5-dione based compounds), after an initial binding of the phenylamine nitrogen lone pair electrons with the Fe3+ haem of the cytochrome P-450, preferentially utilise the region of the AR active site which would normally bind C(17) = O of the substrate. Nitrogen cytochrome P450 family 4 subfamily F member 3 Homo sapiens