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Chinese Academy of Medical Sciences and Peking Union Medical College URAT1 compound 7
- Development stage
- Unknown
- Lead developer
- Chinese Academy of Medical Sciences and Peking Union Medical College
01
Overview
Chinese Academy of Medical Sciences and Peking Union Medical College URAT1 compound 7: sourced facts only. name: "Most compounds potently inhibit the human URAT1 in HEK293 cells, and the most active compound 7 exhibited an IC50 of 0.72 μM, which was much more potent than Lesinurad and comparable to Benzbromarone." [PMID:40669671]; target: "Most compounds potently inhibit the human URAT1 in HEK293 cells, and the most active compound 7 exhibited an IC50 of 0.72 μM, which was much more potent than Lesinurad and comparable to Benzbromarone." [PMID:40669671]; developer: "Beijing Key Laboratory of Active Substance Discovery and Druggability Evaluation, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China." [PMID:40669671]
02
Targets
URAT1 (Uric Acid Transporter 1)
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