PI4KA inhibitor A1

CAS No. 1416334-69-4

PI4KA inhibitor A1( GSK-A1 )

Catalog No. M11735 CAS No. 1416334-69-4

PI4KA inhibitor A1 (GSK-A1) is a highly specific and potent inhibitor of PI4KA.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 151 Get Quote
10MG 302 Get Quote
25MG 537 Get Quote
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    PI4KA inhibitor A1
  • Note
    Research use only, not for human use.
  • Brief Description
    PI4KA inhibitor A1 (GSK-A1) is a highly specific and potent inhibitor of PI4KA.
  • Description
    PI4KA inhibitor A1 (GSK-A1) is a highly specific and potent inhibitor of PI4KA.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    GSK-A1
  • Pathway
    PI3K/Akt/mTOR signaling
  • Target
    PI4K
  • Recptor
    PI4K
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1416334-69-4
  • Formula Weight
    574.631
  • Molecular Formula
    C29H27FN6O4S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : ≥ 2 mg/mL (3.48 mM)
  • SMILES
    O=S(C1=CC(C2=CC=C3C(N(C4=CC=C(N5CCOCC5)C=C4)C(N)=N3)=C2)=CN=C1OC)(NC6=CC=CC=C6F)=O
  • Chemical Name
    5-(2-amino-1-(4-morpholinophenyl)-1H-benzo[d]imidazol-6-yl)-N-(2-fluorophenyl)-2-methoxypyridine-3-sulfonamide

Shipping & Storage Information

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

Reference

1. Bojjireddy N, et al. J Biol Chem. 2014 Feb 28;289(9):6120-32. 2. Alvarez-Prats A, et al. Cell Rep. 2018 Jun 5;23(10):2881-2890.
molnova catalog
related products
  • BQR-695

    BQR-695 (NVP-BQR695) is a highly potent, selective PI4KIIIβ inhibitor that has high potency against both the human (IC50?=?80 nM) and PvPI4K (IC50=3.5 nM).

  • UCT943

    UCT943 (UCT-943) is a potent, selective, next generation Plasmodium falciparum PI4K inhibitor with IC50 of 23 nM.

  • PI-273

    PI-273 (PI273) is a potent, specific, substrate-competitive small molecule inhibitor of PI4KIIα with IC50 of 0.47 uM.