Drug intelligence / Profile preview

isobavachin

Development stage: Unknown
Lead developer: Southern Medical University

Overview

isobavachin: sourced facts only. name: "Isobavachin inhibited URAT1 with an IC50 value of 0.24 ± 0.06 μM, and residues S35, F365, I481 and R477 of URAT1 contributed to high affinity for isobavachin." [PMID:36753966]; target: "Isobavachin inhibited URAT1 with an IC50 value of 0.24 ± 0.06 μM, and residues S35, F365, I481 and R477 of URAT1 contributed to high affinity for isobavachin." [PMID:36753966]; developer: "NMPA Key Laboratory for Research and Evaluation of Drug Metabolism & Guangdong Provincial Key Laboratory of New Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, 1838 Guangzhou Avenue North, Guangzhou, 510515, China." [PMID:36753966]

Targets

URAT1 (Uric Acid Transporter 1)

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