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首页-小分子抑制剂&激动剂-Ras-Raf-MAPK-ERK Pathway-p38 MAPK-SCIO-469
SCIO-469

Chemical Structure : SCIO-469

CAS No.: 309913-83-5

SCIO-469 (Talmapimod;SCIO469;SCIO 469)

货号: PC-42566Not For Human Use, Lab Use Only.

Talmapimod (SCIO469) is a potent, selective p38α MAPK inhibitor with IC50 of 9 nM.

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10 mg ¥1980 In stock
25 mg ¥2980 In stock
50 mg ¥4580 In stock
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

Talmapimod (SCIO469) is a potent, selective p38α MAPK inhibitor with IC50 of 9 nM.
Talmapimod (SCIO469) displays 10-fold selectivity for p38α over p38β, >2,000-fold selectivity over a panel of 20 other kinases, including other MAP kinases.
Talmapimod (SCIO469) decreases apoptosis in MDS CD34+ progenitors and leads to dose-dependant increases in erythroid and myeloid colony formation.
Talmapimod (SCIO469) enhances the ability of MG132 and bortezomib to induce the apoptosis of MM cells, and inhibits tumor growth in vivo.

物理化学性质&存储条件

分子量 513.0035
分子式 C27H30ClFN4O3
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

1H-Indole-3-acetamide, 6-chloro-5-[[(2R,5S)-4-[(4-fluorophenyl)methyl]-2,5-dimethyl-1-piperazinyl]carbonyl]-N,N,1-trimethyl-α-oxo-

参考文献

1. Navas TA, et al. Leukemia. 2006 Jun;20(6):1017-27.

2. Navas TA, et al. Blood. 2006 Dec 15;108(13):4170-7.

3. Hideshima T, et al. Oncogene. 2004 Nov 18;23(54):8766-76.

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