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Product Name | DMH-1 |
Description | Selective inhibitor of bone morphogenic protein (BMP) type-I receptor activin receptor-like kinase 2 (ALK2) receptor (IC50 = 108 nM [Hao et al., 2010] or 12.6 nM [Mohedas et al., 2013] in in vitro kinase assays). Exhibits 6- and 19-fold selectivity for ALK-2 over ALK-1 and ALK-3, respectively, and no significant inhibition of AMPK, ALK5, KDR (VEGFR-2) or PDGFRβ receptors. Blocks BMP4-induced phosphorylation of Smads 1, 5 and 8 in HEK293 cells. Promotes neurogenesis in human induced pluripotent stem cells (iPSCs) when used in combination with SB 431542 (Cat. No. 1614). Purity 98%. MW (observed): 380.44 |
Size | 10 mg |
Concentration | n/a |
Applications | n/a |
Other Names | 4-[6-[4-(1-Methylethoxy)phenyl]pyrazolo[1,5-a]pyrimidin-3-yl]-quinoline |
Gene, Accession, CAS # | CAS: 1206711-16-1 |
Catalog # | 4126/10 |
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Order / More Info | DMH-1 from TOCRIS BIOSCIENCE
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Product Specific References | PubMed: 23563587, 23928500, 25579684, 25806427, 26110906, 26215036, 26655496, 27320041 |
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