BMS-986202
目录号: PL03255 纯度: ≥99%
CAS No. :1771691-34-9
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中文名称
BMS-986202
英文名称
BMS-986202
英文别名
BMS-986202;J2Q5XQZ64C;BDBM50565986;BMS986202;3-Pyridinecarboxamide, 6-((cyclopropylcarbonyl)amino)-4-((3-(5-fluoro-2-pyrimidinyl)-2-methoxyphenyl)amino)-N-(methyl-d3)-;6-((Cyclopropylcarbonyl)amino)-4-((3-(5-fluoro-2-pyrimidinyl)-2-methoxyphenyl)amino)-N-(methyl-d3)-3-pyridinecarboxamide;Unii-J2Q5xqz64C
Cas No.
1771691-34-9
分子式
C22H21FN6O3
分子量
439.46
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
BMS-986202 是一种有效的,选择性的,具有口服活性的 Tyk2 抑制剂,可与 Tyk2 JH2 结合,IC50 为 0.19 nM,Ki 为 0.02 nM。BMS-986202 对包括 Jak 家族成员在内的其他激酶具有高度选择性。BMS-986202 还是 CYP2C19 的弱抑制剂,IC50 为 14 μM。BMS-986202 可用于 IL-23 驱动的棘皮症,抗 CD40 诱导的结肠炎和自发性狼疮的研究。
生物活性
BMS-986202 is a potent, selective and orally active Tyk2 inhibitor that binds to Tyk2 JH2 with an IC50 of 0.19 nM and a Ki of 0.02 nM. BMS-986202 is remarkably selective over other kinases including Jak family members. BMS-986202 is also a weak inhibitor of CYP2C19 with an IC50 of 14 μM. BMS-986202 can be used for IL-23-driven acanthosis, anti-CD40-induced colitis, and spontaneous lupus research[1].
性状
Solid
IC50 & Target[1][2]
Tyk2 JH2 0.19 nM (IC50) Tyk2 JH2 0.02 nM (
体外研究(In Vitro)
BMS-986202 inhibits IFNα and IL-23 in Kit225 T cells with IC50 values of 10 nM and 12 nM, respectively.
BMS-986202 is potent in the IFNα stimulated STAT5 phosphorylation human whole blood (hWB) assay and mouse whole blood (mWB) with IC50 values of 58 nM and 481 nM, respectively. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
BMS-986202 (Compound 7; 3-30 mg/kg; p.o.; daily; for 9 days) treatment inhibits IL-23-driven acanthosis in mice.
BMS-986202 (Compound 7; 0.4-10 mg/kg; p.o.) treatment inhibits IL-12/IL-18-induced IFNγ production in mice. BMS-986202 dose-dependently inhibits IFNγ production by 46% and 80% at doses of 2 mg/kg and 10 mg/kg, respectively.
BMS-986202 (Compound 7; 7-10 mg/kg; p.o.) is stable in liver microsomes, with half lives of greater than 120 min in mouse, rat, monkey, and humans and 89 min in dog. The serum protein binding for BMS-986202 in these species ranges from 89.3% to 96.0%, leaving a good range of free fraction of drug available. BMS-986202 shows the oral bioavailability up to 62-100%. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
ClinicalTrial
参考文献
[1]. Chunjian Liu, et al. Discovery of BMS-986202: A Clinical Tyk2 Inhibitor that Binds to Tyk2 JH2. J Med Chem. 2021 Jan 14;64(1):677-694.
溶解度数据
In Vitro: DMSO : 250 mg/mL (568.88 mM; Need ultrasonic)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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