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BI-6901
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
BI-6901图片
规格:98%
分子量:453.56
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议

产品介绍
BI-6901 是一种有效的选择性CCR10 拮抗剂 (pIC50=9.0)。BI-6901 对其他 GPCRs 表现出高选择性,包括许多其他趋化因子受体。BI-6901 对接触性超敏小鼠 DNFB 模型有效,可用于炎症研究。
货号:ajcx33672
CAS:2040401-92-9
分子式:C23H27N5O3S
分子量:453.56
溶解度:N/A
纯度:98%
存储:Store at -20°C
库存:现货

Background:

BI 6901 is a potent, selective CCR10 antagonist (pIC50=9.0). BI 6901 shows high selectivity over other GPCRs, including a number of other chemokine receptors. BI 6901 is efficacious in the murine DNFB model of contact hypersensitivity and can be used for inflammation research[1].

BI-6901 (intraperitoneal injection; 100 mg/kg; bid.) exhibits a dose-dependent anti-inflammatory response against DNFB stimulated ear swelling in sensitized mice. The level of efficacy observed for BI-6901 is similar to that observed with anti-CCL27 antibody in the same model (60-85%)[1].

[1]. Asitha Abeywardane, et al. N-Arylsulfonyl-α-amino carboxamides are potent and selective inhibitors of the chemokine receptor CCR10 that show efficacy in the murine DNFB model of contact hypersensitivity. Bioorg Med Chem Lett. 2016 Nov 1;26(21):5277-5283.