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Merck
CN

559388

SB 202190

≥98% (HPLC), solid, p38 MAP kinase inhibitor, Calbiochem®

别名:

SB 202190

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关于此项目

经验公式(希尔记法):
C20H14FN3O
化学文摘社编号:
分子量:
331.34
UNSPSC Code:
12352202
NACRES:
NA.77
MDL number:
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产品名称

SB 202190, SB 202190, CAS 152121-30-7, is a potent, reversible, competitive inhibitor of p38. Inhibits p38 phosphorylation of myelin basic protein. Blocks the activity of p38β (Ki = 16 nM; IC50 = 350 nM).

SMILES string

Fc1ccc(cc1)C2=C(NC(=C4C=CC(=O)C=C4)N2)c3ccncc3

InChI

1S/C20H14FN3O/c21-16-5-1-13(2-6-16)18-19(14-9-11-22-12-10-14)24-20(23-18)15-3-7-17(25)8-4-15/h1-12,23-24H

InChI key

NJNKPVPFGLGHPA-UHFFFAOYSA-N

assay

≥98% (HPLC)

form

solid

potency

16 nM Ki

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
protect from light

color

pale yellow

solubility

DMSO: 50 mg/mL

shipped in

ambient

storage temp.

−20°C

Quality Level

Biochem/physiol Actions

主要靶标
p38β
产物与ATP竞争。
可逆性:是
细胞可渗透性:是
靶标IC50:针对p38β的激酶活性,为350 nM;针对激活转录因子2(ATF-2)的p38磷酸化,为280 nM

Disclaimer

毒性:标准处理(A)

General description

一种有效的、可逆的、竞争性的、细胞渗透性p38 MAP激酶抑制剂。抑制髓鞘碱性蛋白(MBP)的p38磷酸化,而不影响ERK或JNK MAP激酶亚群的活性。还抑制p38β的激酶活性(Ki=16 nM;IC50=350 nM)和激活转录因子2的p38磷酸化(ATF-2;IC50=280 nM)。阻断LPS诱导的TNF-α和白细胞介素生物合成已报道在Hep52细胞中诱导LDL受体表达。也可提供SB 202190(目录号559397)在无水DMSO中的1 mg/ml溶液。

Other Notes

Davies, S.P., et al. 2000.Biochem.J.351, 95.
Ajizian, S.J., et al. 1999.J. Infect.Dis.179, 939.
Singh, R.P., et al. 1999.J. Biol. Chem.274, 19593.
Wang, S.W., et al. 1999.Inflamm.Res.48, 533.
Gallagher, T.F., et al. 1997.Bioorg.Med. Chem. 5, 49.
LoGrasso, P.V., et al. 1997.Biochem.36, 10422.
Jiang, Y., et al. 1996.J. Biol. Chem. 271, 17920.
Kramer, R.M., et al. 1996.J. Biol. Chem.271, 27723.
Li, Z., et al. 1996.Biochem.Biophys.Res.Commun.228, 334.
Lee, J.C., et al. 1994.Nature 372, 739.

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6个月。

Legal Information

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

存储类别

11 - Combustible Solids

wgk

WGK 3


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