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- W2006385596 endingPage "207" @default.
- W2006385596 startingPage "195" @default.
- W2006385596 abstract "Xanthine oxidoreductase (XOR), which is widely distributed from humans to bacteria, has a key role in purine catabolism, catalyzing two steps of sequential hydroxylation from hypoxanthine to xanthine and from xanthine to urate at its molybdenum cofactor (Moco). Human XOR is considered to be a target of drugs not only for therapy of hyperuricemia and gout, but also potentially for a wide variety of other diseases. In this review, we focus on studies of XOR inhibitors and their implications for understanding the chemical nature and reaction mechanism of the Moco active site of XOR. We also discuss further experimental or clinical studies that would be helpful to clarify remaining issues." @default.
- W2006385596 created "2016-06-24" @default.
- W2006385596 creator A5011237103 @default.
- W2006385596 creator A5056974084 @default.
- W2006385596 date "2014-12-12" @default.
- W2006385596 modified "2023-10-06" @default.
- W2006385596 title "Mechanistic insights into xanthine oxidoreductase from development studies of candidate drugs to treat hyperuricemia and gout" @default.
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