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- W2946667802 abstract "Many O-glucuronides exhibiting various pharmacological activities have been found in nature and in drug metabolism. The glucuronidation of bioactive natural products or drugs to generate glucuronides with better activity and druggability is important in drug discovery and research. In this study, by using two uridine diphosphate (UDP)-dependent glucuronosyltransferases (GATs, UGT88D4 and UGT88D7) from plants, we developed two glucuronidation approaches, pure enzyme catalysis in vitro and recombinant whole-cell catalysis in vivo, to efficiently synthesize bioactive O-glucuronides by the glucuronidation of natural products. In total, 14 O-glucuronides with different structures, including flavonoids, anthraquinones, coumarins, and lignans, were obtained, 7 of which were new compounds. Furthermore, one of the biosynthesized O-glucuronides, kaempferol-7- O-β-d-glucuronide (3a), potently inhibited protein tyrosine phosphatase (PTP) 1B with an IC50 value of 8.02 × 10-6 M. Some of the biosynthesized O-glucuronides also exhibited significant antioxidant activities." @default.
- W2946667802 created "2019-05-29" @default.
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- W2946667802 date "2019-05-14" @default.
- W2946667802 modified "2023-09-26" @default.
- W2946667802 title "Enzymatic Synthesis of Bioactive <i>O</i>-Glucuronides Using Plant Glucuronosyltransferases" @default.
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- W2946667802 doi "https://doi.org/10.1021/acs.jafc.9b01769" @default.
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