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• W1964156945 abstract "Abstract Analogs submitted by ethyl, n-propyl, n-butyl, and isopropyl groups instead of methyl group adjacent to a ketone group of acetohexamide were synthesized and the structural requirements of carbonyl reductase from rabbit kidney for these analogs were kinetically examined. The hydrophobicities in straight-chain alkyl groups of acetohexamide analogs were found to play an important role in the catalytic activity and substrate-binding capacity of the enzyme. We propose the possibility that a hydrophobic pocket is located in the substrate-binding domain of the enzyme." @default.
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• W1964156945 date "1994-12-01" @default.
• W1964156945 modified "2023-09-25" @default.
• W1964156945 title "Catalytic Properties of Carbonyl Reductase from Rabbit Kidney for Acetohexamide and Its Analogs" @default.
• W1964156945 doi "https://doi.org/10.1006/bioo.1994.1032" @default.
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