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EC Number
Inhibitors
Commentary
Structure
1.14.14.86
CO
90% inhibition
1.14.14.86
DSI-505ME
-
1.14.14.86
methyl (2E)-3-[1-[(1E)-1-(4-chlorophenyl)-3-hydroxy-4,4-dimethylpent-1-en-2-yl]-1H-imidazol-5-yl]prop-2-enoate
-
1.14.14.86
more
not inhibited by uniconazole-P
1.14.14.86
more
among the azoles known as CYP51 inhibitors, ketoconazole, an antifungal medicine, is one of the most potent CYP51 inhibitor and forms a one-to-one complex with CYP51 as with uniconazole and CYP701B1. But ketoconazole does not bind and inhibit the purified ent-kaurene oxidase, CYP701B1; not inhibitory: ketoconazole
1.14.14.86
paclobutrazol
-
1.14.14.86
paclobutrazol racemate
-
1.14.14.86
uniconazole
-
1.14.14.86
uniconazole
i.e. UNI
1.14.14.86
uniconazole
selective binding of CYP701B1 with uniconazole, is directly bound to the heme iron with its azole nitrogen
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