DMH-1

CAS No. 1206711-16-1

DMH-1( DMH1 | DMH 1 )

Catalog No. M10757 CAS No. 1206711-16-1

DMH1 is a potent, selective bone morphogenetic protein receptor (BMP) inhibitor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 60 In Stock
5MG 50 In Stock
10MG 80 In Stock
25MG 155 In Stock
50MG 271 In Stock
100MG 423 In Stock
200MG Get Quote In Stock
500MG 918 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    DMH-1
  • Note
    Research use only, not for human use.
  • Brief Description
    DMH1 is a potent, selective bone morphogenetic protein receptor (BMP) inhibitor.
  • Description
    DMH1 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; 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; reduces the canonical phosphorylation of Smads 1,5 and 9, inhibits HeLa and MCF-7 cell proliferation; significantly reduces the tumor growth in human lung cancer xenograft model.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    DMH1 | DMH 1
  • Pathway
    TGF-beta/Smad
  • Target
    TGFBR
  • Recptor
    ALK2
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1206711-16-1
  • Formula Weight
    380.4418
  • Molecular Formula
    C24H20N4O
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 11.5 mg/mL
  • SMILES
    CC(OC1=CC=C(C2=CN3C(N=C2)=C(C4=CC=NC5=CC=CC=C45)C=N3)C=C1)C
  • Chemical Name
    Quinoline, 4-[6-[4-(1-methylethoxy)phenyl]pyrazolo[1,5-a]pyrimidin-3-yl]-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

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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