PeptideDB

BMS-502

CAS: 2407854-18-4 F: C27H22F2N6O3 W: 516.50

BMS-502 (Compound 22) is a potent dual inhibitor of diacylglycerol kinase (DGK) α and ζ with IC50 of 4.6 nM and 2.1 nM
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Bioactivity BMS-502 (Compound 22) is a potent dual inhibitor of diacylglycerol kinase (DGK) α and ζ with IC50 of 4.6 nM and 2.1 nM. BMS-502 enhanced T cell immune responses in mice. BMS-502 can be used in tumor immunity related research[1].
Target IC50: 4.6 nM (DGK α), 2.1nM (DGK ζ).
Invitro 在小鼠细胞毒性 T 细胞 IFNγ 试验 (mCTC) 中测得的 BMS-502 EC50 值为 340 nM[1]。
In Vivo BMS-502 (Compound 22) (0-10mg/kg; 口服; 24 小时) 在小鼠 OT-1 模型中表现出剂量依赖性免疫刺激作用[1]。 C57 小鼠中药代动力学分析[1]Route
Name BMS-502
CAS 2407854-18-4
Formula C27H22F2N6O3
Molar Mass 516.50
Transport Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Reference [1]. Chupak L, et al. Discovery of Potent, Dual-Inhibitors of Diacylglycerol Kinases Alpha and Zeta Guided by Phenotypic Optimization. ACS Med Chem Lett. 2023 Jun 12;14(7):929-935.