Drug intelligence / Profile preview

DSO-5a

Development stage
Preclinical
Lead developer
Shanghai Jiao Tong University
01

Overview

DSO-5a: sourced facts only. name: "Dimethyl shikonin oxime 5a (DSO-5a) was identified as the most potent agonist for BB3 (pEC50 = 8.422 in IP-1 accumulation), which was 898-fold more potent than DMAKO-00." [PMID:37272653]; target: "Dimethyl shikonin oxime 5a (DSO-5a) was identified as the most potent agonist for BB3 (pEC50 = 8.422 in IP-1 accumulation), which was 898-fold more potent than DMAKO-00." [PMID:37272653]; developer: "State Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences, School of Life Sciences and Biotechnology; Shanghai Jiao Tong University, Shanghai 200240, China." [PMID:37272653]; stage: "Importantly, without brain penetration, DSO-5a improved glucose tolerance in C57BL/6 mice through BB3 and ameliorated glucose homeostasis in diabetic db/db mice." [PMID:37272653]

02

Targets

BRS3 (Bombesin receptor subtype 3)

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