| Popis: |
The novel 10β-aziridinylestr-4-ene-3,17-diones 17 and 18 and the corresponding 10β-aziridinyl-β-hydroxyestr-4-en-3-ones 19 and 20 have been synthesized from the 19-oximino-19-methyl intermediate 12b. The key reaction was the conversion of the 19-oxime 12b into the diastereoisomeric 1OR-aziridines 13 and 14 by lithium aluminium hydride (LAH). Compounds 17–20 are powerful and stereoselective inhibitors of human placental microsomal aromatase. The most potent compound was 17(Ki = 3.4 nmol dm–3). The 19R- isomers 17 and 19 are more effective than the corresponding 19S-isomers 18 and 20, respectively. Unlike the corresponding 10β-oxiranes and -thiiranes which are classical competitive inhibitors, the (19R)-aziridines 17 and 19 appear to be slow-binding inhibitors. Spectroscopic studies with microsomal aromatase preparations indicate that the inhibition process involves binding of aziridine nitrogen to the heme-iron of the enzyme. |
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