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首页-小分子抑制剂&激动剂-Ras-Raf-MAPK-ERK Pathway-MAPKAPK2 (MK2)-MK2-IN-1 hydrochloride
MK2-IN-1 hydrochloride

Chemical Structure : MK2-IN-1 hydrochloride

CAS No.: 1314118-94-9

MK2-IN-1 hydrochloride (MK2 Inhibitor)

货号: PC-43244Not For Human Use, Lab Use Only.

MK2-IN-1 is a potent, selecitve, non-ATP competitive MAPKAPK2 (MK2) inhibitor with IC50 of 0.11 uM.

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10 mg ¥3280 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

MK2-IN-1 hydrochloride is a potent, selecitve, non-ATP competitive MAPKAPK2 (MK2) inhibitor with IC50 of 0.11 uM.
MK2-IN-1 shows excellent kinase selectivity against a broad panel of 150 protein kinases at 10 μM with only on exception of CK1γ3 >50 % inhibition.
MK2-IN-1 inhibits pro-inflammatory cytokine secretion from the human THP1 acute monocytic leukemia cell line, causing dose-dependent inhibition of LPS-stimulated TNFα and IL6 secretion.
MK2-IN-1 also dose dependently inhibits IL1β-stimulated MMP13 secretion from the SW1353 chondrosarcoma cell line and human primary chondrocyte cultures.

物理化学性质&存储条件

分子量 509.4269
分子式 C27H26Cl2N4O2
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

Chemical Name/SMILES

2-Furancarboxamide, 5-(4-chlorophenyl)-N-[4-(1-piperazinyl)phenyl]-N-(2-pyridinylmethyl)-, hydrochloride (1:1)

参考文献

1. Rao AU, et al. Bioorg Med Chem Lett. 2012 Jan 15;22(2):1068-72.

2. Huang X, et al. Bioorg Med Chem Lett. 2012 Jan 1;22(1):65-70.

3. Huang X, et al. ACS Med Chem Lett. 2011 Jun 24;2(8):632-7.

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