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Merck
CN

553502

NSC23766 trihydrochloride

≥93% (HPLC), lyophilized, Rac1 inhibitor, Calbiochem®

别名:

NSC23766, Rac1抑制剂

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关于此项目

经验公式(希尔记法):
C24H38Cl3N7
化学文摘社编号:
分子量:
530.96
MDL number:
UNSPSC Code:
12352200
NACRES:
NA.77
Assay:
≥93% (HPLC)
Form:
lyophilized
Quality level:
Storage condition:
OK to freeze, desiccated (hygroscopic), protect from light
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产品名称

Rac1抑制剂, Rac1 Inhibitor, CAS 1177865-17-6, is a cell-permeable, reversible inhibitor of Rac1 GDP/GTP exchange. Interferes with the interaction between Rac1 and Rac-specific GEFs Trio and Tiam1 (IC50 ~50 µM).

Quality Level

assay

≥93% (HPLC)

form

lyophilized

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, desiccated (hygroscopic), protect from light

solubility

water: 5 mg/mL

shipped in

ambient

storage temp.

2-8°C

SMILES string

Cl.Cl.Cl.N(CCCC(Nc1nc(cc(n1)C)Nc2cc3c(nc(cc3N)C)cc2)C)(CC)CC

InChI

1S/C24H35N7.3ClH/c1-6-31(7-2)12-8-9-16(3)27-24-28-18(5)14-23(30-24)29-19-10-11-22-20(15-19)21(25)13-17(4)26-22;;;/h10-11,13-16H,6-9,12H2,1-5H3,(H2,25,26)(H2,27,28,29,30);3*1H

InChI key

CPUHORIUXPQCHW-UHFFFAOYSA-N

General description

一种细胞渗透性嘧啶化合物,通过干扰Rac1和Rac特异性GEF(鸟嘌呤核苷酸交换因子)Trio和Tiam1(IC50 ~50 µM)之间的相互作用,特异性和可逆地抑制Rac1 GDP/GTP交换活性。显示有效抑制NIH3T3和PC-3细胞中Rac1介导的细胞功能(有效剂量~50至100 μM)。对Cdc42或RhoA激活无影响,且不影响Rac1与BcrGAP或PAK1的相互作用。减少TRAP诱导和胶原刺激的血小板聚集(IC50分别为50 mM和64 mM)。

Biochem/physiol Actions

主要靶标
Rac1
产物不与ATP竞争。
可逆性:是
细胞可渗透性:是
靶标IC50:针对Rac1 GDP/GTP交换活性约为50µM;针对TRAP诱导和胶原蛋白刺激的血小板聚集为50 mM和64 mM

Packaging

用惰性气体包装

Preparation Note

复溶后,等分并冷冻保存(-20°C)。贮备溶液在-20°C下可稳定保存至多3个月。

Other Notes

Dwivedi, S., et al. 2010.J. Translational Med.8, 128.
Desire, L., et al. 2005.J. Biol. Chem.280, 37516.
Gao, Y., et al. 2004.Proc.Natl.Acad.Sci. USA101, 7618.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

毒性:致癌/致畸(D)


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存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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全球贸易项目编号

货号GTIN
553502-10MG04055977193626
553502-5MG07790788051433