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首页-小分子抑制剂&激动剂-Tyrosine Kinase-c-Fms (CSF1R)-Ki20227
Ki20227

Chemical Structure : Ki20227

CAS No.: 623142-96-1

Ki20227 (Ki 20227;Ki-20227)

货号: PC-42568Not For Human Use, Lab Use Only.

Ki20227 is a potent, selective, orally active c-Fms inhibitor with IC50 of 2 nM.

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10 mg ¥1780 In stock
25 mg ¥2980 In stock
50 mg ¥4880 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

Ki20227 is a potent, selective, orally active c-Fms (CSF1R) inhibitor with IC50 of 2 nM.
Ki20227 weakly inhibits KDR, c-Kit, and PDGFRβ with IC50 of 12, 451, and 217 nM, respectively, no activty against Flt-3, c-Src, Fyn, EGFR, FGFR2, Met, Btk, PKA, and PKCα (IC50>1,000 nM).
Ki20227 inhibits the M-CSF-dependent cell growth, suppresses osteoclast differentiation and osteolytic bone destruction in a bone metastasis model.

物理化学性质&存储条件

分子量 480.5362
分子式 C24H24N4O5S
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: 7.2 mg/mL

Chemical Name/SMILES

Urea, N-[4-[(6,7-dimethoxy-4-quinolinyl)oxy]-2-methoxyphenyl]-N'-[1-(2-thiazolyl)ethyl]-

参考文献

1. Ohno H, et al. Mol Cancer Ther. 2006 Nov;5(11):2634-43.

2. Ohno H, et al. Eur J Immunol. 2008 Jan;38(1):283-91.

3. Uemura Y, et al. J Neuroimmunol. 2008 Mar;195(1-2):73-80.

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