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GSK2983559 free acid Sale

目录号 : GC38037

A RIPK2 inhibitor

GSK2983559 free acid Chemical Structure

Cas No.:1579965-12-0

规格 价格 库存 购买数量
1mg
¥765.00
现货
5mg
¥2,250.00
现货
10mg
¥3,690.00
现货
25mg
¥7,380.00
现货
50mg
¥13,680.00
现货
100mg
¥22,050.00
现货
200mg 待询 待询
500mg 待询 待询

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Sample solution is provided at 25 µL, 10mM.

产品文档

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产品描述

GSK2983559 is a receptor-interacting protein kinase 2 (RIPK2) inhibitor.1 It inhibits RIPK2 by 65% in a kinase assay when used at a concentration of 10 ?M. GSK2983559 (10 ?M) also inhibits VEGFR3 by greater than 90%, as well as 14 additional kinases by 60 to 89% in a panel of 344 kinases. In vivo, GSK2983559 (7.5 and 145 mg/kg twice per day) reduces colonic damage in a mouse model of TNBS-induced colitis. GSK2983559 is also a prodrug that is cleaved to an active metabolite in the gastrointestinal tract that inhibits RIPK2 more potently than GSK2983559.

1.Haile, P.A., Casillas, L.N., Votta, B.J., et al.Discovery of a first-in-class receptor interacting protein 2 (RIP2) kinase specific clinical candidate, 2-((4-(benzo[d]thiazol-5-ylamino)-6-(tert-butylsulfonyl)quinazolin-7-yl)oxy)ethyl dihydrogen phosphate, for the treatment of inflammatory diseasesJ. Med. Chem.62(14)6482-6494(2019)

Chemical Properties

Cas No. 1579965-12-0 SDF
Canonical SMILES CC(C)(C)S(C(C(OCCOP(O)(O)=O)=CC1=NC=N2)=CC1=C2NC3=CC(N=CS4)=C4C=C3)(=O)=O
分子式 C21H23N4O7PS2 分子量 538.53
溶解度 DMSO: 5 mg/mL (9.28 mM; ultrasonic and warming and heat to 80°C) 储存条件 Store at -20°C
General tips 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
Shipping Condition 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。

溶解性数据

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1 mg 5 mg 10 mg
1 mM 1.8569 mL 9.2845 mL 18.5691 mL
5 mM 0.3714 mL 1.8569 mL 3.7138 mL
10 mM 0.1857 mL 0.9285 mL 1.8569 mL
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