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首页-小分子抑制剂&激动剂-Ras-Raf-MAPK-ERK Pathway-p38 MAPK-LY2228820 dimesylate
LY2228820 dimesylate

Chemical Structure : LY2228820 dimesylate

CAS No.: 862507-23-1

LY2228820 dimesylate (Ralimetinib dimesylate, LY-2228820)

货号: PC-43421Not For Human Use, Lab Use Only.

LY2228820 dimesylate (Ralimetinib) is a potent, selective, orally available inhibitor p38 MAPK with IC50 of 5.3 and 3.2 nM for p38α and p38β, respectively.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

LY2228820 dimesylate (Ralimetinib) is a potent, selective, orally available inhibitor p38 MAPK with IC50 of 5.3 and 3.2 nM for p38α and p38β, respectively.
LY2228820 dimesylate (Ralimetinib) potently and selectively inhibits phosphorylation of MK2 (Thr334) in anisomycin-stimulated HeLa cells and mouse RAW264.7 macrophages (IC50=35.3 nM), with no changes in phosphorylation of p38α MAPK, JNK, ERK1/2, c-Jun, ATF2, or c-Myc.
LY2228820 dimesylate (Ralimetinib) also reduces TNF-α secretion by LPS/IFN-γ–stimulated macrophages with IC50 of 6.3 nM.
LY2228820 dimesylate (Ralimetinib) produces significant tumor growth delay in multiple in vivo cancer models (melanoma, non-small cell lung cancer, ovarian, glioma, myeloma, breast).

物理化学性质&存储条件

分子量 612.737
分子式 C26H37FN6O6S2
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

DMSO: < 7.8 mg/mL

Chemical Name/SMILES

3H-Imidazo[4,5-b]pyridin-2-amine, 5-[2-(1,1-dimethylethyl)-4-(4-fluorophenyl)-1H-imidazol-5-yl]-3-(2,2-dimethylpropyl)-, methanesulfonate (1:2)

参考文献

1. Tate CM, et al. J Biol Chem. 2013 Mar 1;288(9):6743-53.

2. Campbell RM, et al. Mol Cancer Ther. 2014 Feb;13(2):364-74.

3. Ishitsuka K, et al. Br J Haematol. 2008 May;141(5):598-606.

4. Patnaik A, et al. Clin Cancer Res. 2016 Mar 1;22(5):1095-102.

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