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Merck
CN

662005

U0126

≥98% (HPLC), solid, MEK inhibitor, Calbiochem®

别名:

U0126, 1,4-二氨基-2,3-二氰基-1,4-(2-氨基苯巯基)丁二烯,d,MEK抑制剂VI

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关于此项目

经验公式(希尔记法):
C18H16N6S2 · 0.5C2H6O
化学文摘社编号:
分子量:
403.52
MDL number:
UNSPSC Code:
12352200
NACRES:
NA.77
Assay:
≥98% (HPLC)
Form:
solid
Quality level:
Storage condition:
OK to freeze, protect from light
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产品名称

U0126, U0126, CAS 109511-58-2, is a potent and specific inhibitor of MEK1 (IC50 = 72 nM) and MEK2 (IC50 = 58 nM). The inhibition is noncompetitive with respect to both ATP and ERK.

Quality Level

assay

≥98% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, protect from light

color

white

solubility

DMSO: 200 mg/mL

shipped in

ambient

storage temp.

−20°C

SMILES string

S(c2c(cccc2)N)\C(=C(\C(=C(\Sc1c(cccc1)N)/N)\C#N)/C#N)\N

InChI

1S/C18H16N6S2/c19-9-11(17(23)25-15-7-3-1-5-13(15)21)12(10-20)18(24)26-16-8-4-2-6-14(16)22/h1-8H,21-24H2/b17-11+,18-12+

InChI key

DVEXZJFMOKTQEZ-JYFOCSDGSA-N

General description

MEK1(IC50=72 nM)和MEK2(IC50=58 nM)的有效和特异性抑制剂。这种抑制对ATP和ERK都是非竞争性的。对其他激酶如Abl、Cdk2、Cdk4、ERK、JNK、MEKK、MKK-3、MKK-4/SEK、MKK-6、PKC和Raf几乎没有影响。显示可阻断多沙唑嗪诱导的成骨细胞分化。也可作为免疫抑制剂,有效阻断IL-2合成和T细胞增殖,而不影响T细胞活化或耐受的长期结果。对于ATP没有竞争性。也可提供InSolution格式(目录号662009)。

Biochem/physiol Actions

主靶
MEK1和MEK2
产物不与ATP竞争。
可逆:否
细胞可渗透性:否
靶标IC50:针对MEK1和MEK2分别为72和58nM。

Packaging

用惰性气体包装

Preparation Note

溶液中不稳定;仅在使用前进行复溶。

Other Notes

Choi, Y.J., et al. 2011.Biochem.Biophys.Res. Commun.416, 232.
DeSilva, D.R., et al. 1998.J. Immunol. 160, 4175.
Duncia, J.V., et al. 1998.Biorg.Med. Chem. Lett.8, 2839.
Favata, M.F., et al. 1998.J. Biol. Chem. 273, 18623.

Legal Information

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

Disclaimer

毒性:标准处理(A)


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存储类别

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable



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全球贸易项目编号

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