Home - Products - Angiogenesis - ALK - 5-phenylthieno[2,3-d]pyrimidin-4-amine

5-phenylthieno[2,3-d]pyrimidin-4-amine

CAS No. 195193-10-3

5-phenylthieno[2,3-d]pyrimidin-4-amine( —— )

Catalog No. M28408 CAS No. 195193-10-3

5-phenylthieno[2,3-d]pyrimidin-4-amine is a chemical compound.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 57 Get Quote
5MG 87 Get Quote
10MG 131 Get Quote
25MG 224 Get Quote
50MG 336 Get Quote
100MG 503 Get Quote
500MG 1107 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    5-phenylthieno[2,3-d]pyrimidin-4-amine
  • Note
    Research use only, not for human use.
  • Brief Description
    5-phenylthieno[2,3-d]pyrimidin-4-amine is a chemical compound.
  • Description
    5-phenylthieno[2,3-d]pyrimidin-4-amine is a chemical compound.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Angiogenesis
  • Target
    ALK
  • Recptor
    RARγ
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    195193-10-3
  • Formula Weight
    227.285
  • Molecular Formula
    C12H9N3S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    Nc1ncnc2scc(-c3ccccc3)c12
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.M I Dawson, et al. Retinoic acid (RA) receptor transcriptional activation correlates with inhibition of 12-O-tetradecanoylphorbol-13-acetate-induced ornithine decarboxylase (ODC) activity by retinoids: a potential role for trans-RA-induced ZBP-89 in ODC inhibition. Int J Cancer. 2001 Jan 1;91(1):8-21.
molnova catalog
related products
  • SB-505124 hydrochlor...

    SB-505124 hydrochloride (SB505124 hydrochloride) is an orally available, selective and potent inhibitor of TGF-β type I receptors (ALK4, ALK5, ALK7) with IC50 values of 129 nM and 47 nM for ALK4 and ALK5, respectively.

  • Ascrinvacumab

    Ascrinvacumab (PF-03446962) is a highly humanized IgG2 monoclonal antibody against ALK-1 with a Kd value of 7 nM for human ALK1.

  • LDK378 dihydrochlori...

    Ceritinib dihydrochloride is a selective, orally bioavailable and ATP-competitive inhibitor of ALK tyrosine kinase(IC50 of 200 pM), and also inhibits IGF-1R, InsR, and STK22D (IC50 values of 8, 7, and 23 nM, respectively).