BRK inhibitor P21d hydrochloride
目录号: PL08301
CAS No. :2250025-98-8
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中文名称
BRK inhibitor P21d hydrochloride
英文名称
BRK inhibitor P21d hydrochloride
英文别名
Methanone, [4-[[6-cyclopropyl-3-(1H-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]amino]-3-fluorophenyl]-4-morpholinyl-, hydrochloride (1:1);BRK inhibitor P21d hydrochloride
Cas No.
2250025-98-8
分子式
C23H23ClFN7O2
分子量
483.93
包装储存
-20°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
产品详情
BRK inhibitor P21d hydrochloride 是一种有效的乳腺肿瘤激酶 ( BRK/PTK6) 抑制剂,IC50 为 30 nM。BRK inhibitor P21d hydrochloride 抑制 p-SAM68,IC50 为 52 nM。BRK inhibitor P21d hydrochloride 可用于评估 BRK 抑制剂在异种移植乳腺肿瘤模型中的体内活性。
生物活性
BRK inhibitor P21d hydrochloride is a potent breast tumor kinase (BRK/PTK6) inhibitor with an IC 50 of 30 nM. BRK inhibitor P21d hydrochloride inhibits p-SAM68 with an IC 50 of 52 nM. BRK inhibitor P21d hydrochloride can be used to evaluate the in vivo activity of BRK inhibitors in xenograft breast tumor models.
性状
Solid
IC50 & Target[1][2]
IC50: 30 nM (BRK), 52 nM (p-SAM68), >20 μM (Aurora B), >20 μM (Lck)
体外研究(In Vitro)
BRK inhibitor P21d hydrochloride (compound 21d) inhibits Aurora B (IC50>20 μM) and Lck (IC50>20 μM). has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
BRK inhibitor P21d hydrochloride (compound 21d) has much better permeability (CACO-2:314 nm/s) and PK profile (rat, po, 10 mpk, AUC 0–6h =31.1 μM?h,C 6h =3.5 μM). 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
-20°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
参考文献
[1]. Hongbo Zeng, et al. Discovery of Novel imidazo[1,2-a]pyrazin-8-amines as Brk/PTK6 Inhibitors. Bioorg Med Chem Lett. 2011 Oct 1;21(19):5870-5.
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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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