Chemical Structure : DMH-1
CAS No.: 1206711-16-1
货号: PC-42935Not For Human Use, Lab Use Only.
DMH-1 is a potent, selective bone morphogenetic protein receptor (BMP) inhibitor with IC50 of 27/107.9/<5/47.6 nM for ALK1/ALK2/ALK3/ALK6, respectively.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | ¥780 | In stock | |
25 mg | ¥1380 | In stock | |
50 mg | ¥2280 | In stock | |
100 mg | Get quote |
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DMH-1 is a potent, selective bone morphogenetic protein receptor (BMP) inhibitor with IC50 of 27/107.9/<5/47.6 nM for ALK1/ALK2/ALK3/ALK6, respectively.
DMH-1 significantly reduces the percentage of cells expressing the pluripotency marker proteins OCT4 and Nanog in both SM3 and CA6 cells, induces regulation of pluripotency and neural precursor marker mRNAs.
DMH-1 reduces the canonical phosphorylation of Smads 1,5 and 9, inhibits HeLa and MCF-7 cell proliferation;.
DMH-1 significantly reduces the tumor growth in human lung cancer xenograft model.
分子量 | 380.4418 | |
分子式 | C24H20N4O | |
外观性状 | Solid | |
储存条件 |
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Solubility |
DMSO: 11.5 mg/mL |
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Chemical Name/SMILES |
Quinoline, 4-[6-[4-(1-methylethoxy)phenyl]pyrazolo[1,5-a]pyrimidin-3-yl]- |
1. Hao J, et al. ACS Chem Biol. 2010 Feb 19;5(2):245-53.
2. Cross EE, et al. ACS Chem Biol. 2011 Sep 16;6(9):952-61.
3. Hao J, et al. PLoS One. 2014 Mar 6;9(6):e90748.
4. Engers DW, et al. Bioorg Med Chem Lett. 2013 Jun 1;23(11):3248-52.
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