Title : Enhancing in vivo oral bioavailability of cajaninstilbene acid using UDP-glucuronosyl transferase inhibitory excipient containing self-microemulsion.

Pub. Date : 2020 Sep

PMID : 32371286






1 Functional Relationships(s)
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1 In the present study, we utilize UGT inhibitory excipient containing self-microemulsion (SME) delivery system to reduce the production of glucuronide metabolites and increase its oral bioavailability. Glucuronides UDP glycosyltransferase 2 family, polypeptide B Rattus norvegicus