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HS271 Sale

目录号 : GC62429

HS271 是一个强效的、口服有效的、选择性的 IRAK4 抑制剂,其 IC50 值为 7.2 μM。HS271 具有优越的体外酶活性和细胞活性,同时也表现出极好的药代动力学特征。

HS271 Chemical Structure

Cas No.:2410393-15-4

规格 价格 库存 购买数量
10mM (in 1mL DMSO)
¥3,465.00
现货
5 mg
¥3,150.00
现货
10 mg
¥5,220.00
现货
25 mg
¥9,900.00
现货
50 mg
¥15,300.00
现货
100 mg
¥22,500.00
现货

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Sample solution is provided at 25 µL, 10mM.

产品文档

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产品描述

HS271 is a highly potent, orally active and selective IRAK4 inhibitor, with an IC50 of 7.2 μM. HS271 exhibits superior enzymatic and cellular activities, as well as excellent pharmacokinetic properties[1].

HS271 (15-150 mg/kg) displays robust in vivo antiinflammatory efficacy as evaluated in rat models of LPS induced TNFα production collageninduced arthritis[1].HS271 exhibits a t1/2 of 3.3 h and Cmax of 2107 ng/mL[1].HS271 is stable in liver microsome assays across other species, including rat, mouse, monkey, and human[1].HS271 exhibits oral bioavailability of 67.3%, 58.2%, 14.4&% and 49% in mouse, rat, dog and monkey, respectively[1].

[1]. Wenqiang Zhai, et al. Discovery and optimization of a potent and selective indazolamine series of IRAK4 inhibitors. Bioorg Med Chem Lett. 2020 Nov 24;31:127686.

Chemical Properties

Cas No. 2410393-15-4 SDF
分子式 C21H24F3N5O2 分子量 435.44
溶解度 DMSO : 100 mg/mL (229.65 mM; Need ultrasonic) 储存条件 Store at -20°C
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.2965 mL 11.4826 mL 22.9653 mL
5 mM 0.4593 mL 2.2965 mL 4.5931 mL
10 mM 0.2297 mL 1.1483 mL 2.2965 mL
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Research Update

Discovery and optimization of a potent and selective indazolamine series of IRAK4 inhibitors

Bioorg Med Chem Lett 2021 Jan 1;31:127686.PMID:33242574DOI:10.1016/j.bmcl.2020.127686

IRAK4 is a key mediator of innate immunity. There is a high interest in identifying novel IRAK4 inhibitors for the treatment of inflammatory autoimmune diseases. We describe here a highly potent and selective IRAK4 inhibitor (HS271) that exhibited superior enzymatic and cellular activities, as well as excellent pharmacokinetic properties. HS271 displayed robust in vivo anti-inflammatory efficacy as evaluated in rat models of LPS induced TNFα production and collagen-induced arthritis.