K02288

CAS No. 1431985-92-0

K02288( K 02288 | K-02288 )

Catalog No. M11838 CAS No. 1431985-92-0

K02288 is a potent, selective inhibitor of BMP signaling.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 55 In Stock
2MG 31 In Stock
5MG 49 In Stock
10MG 85 In Stock
25MG 157 In Stock
50MG 269 In Stock
100MG 398 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    K02288
  • Note
    Research use only, not for human use.
  • Brief Description
    K02288 is a potent, selective inhibitor of BMP signaling.
  • Description
    K02288 is a potent, selective inhibitor of BMP signaling with IC50 of 1.8/1.1/34.4/6.3 nM for ALK/1/2/3/6, displays 300-fold selectivity for ALK2 over the TGF-β receptor ALK5 and ALK4; also wekaly inhibits type II BMP receptor ActRIIA (IC50=220 nM); specifically inhibits the BMP-induced Smad pathway without affecting TGF-β signaling and induces dorsalization of zebrafish embryos; inhibits BMP9-induced phosphorylation of SMAD1/5/8 in HUVECs to reduce both the SMAD and the Notch-dependent transcriptional responses, inhibits functional angiogenesis.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    K 02288 | K-02288
  • Pathway
    TGF-beta/Smad
  • Target
    TGFBR
  • Recptor
    ALK1|ALK2|ALK3|ALK4|ALK6
  • Research Area
    Other Indications
  • Indication
    ——

Chemical Information

  • CAS Number
    1431985-92-0
  • Formula Weight
    352.3838
  • Molecular Formula
    C20H20N2O4
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 58.6 mg/mL
  • SMILES
    OC1=CC=CC(C2=CC(C3=CC(OC)=C(OC)C(OC)=C3)=C(N)N=C2)=C1
  • Chemical Name
    Phenol, 3-[6-amino-5-(3,4,5-trimethoxyphenyl)-3-pyridinyl]-

Shipping & Storage Information

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

Reference

1. Sanvitale CE, et al. PLoS One. 2013 Apr 30;8(4):e62721. 2. Mohedas AH, et al. J Med Chem. 2014 Oct 9;57(19):7900-15. 3. Kerr G, et al. Angiogenesis. 2015 Apr;18(2):209-17. 4. Windhausen T, et al. Molecules. 2015 Apr 24;20(5):7586-601.
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