trans-isrib A17

CAS No. 1628478-15-8

trans-isrib A17( —— )

Catalog No. M35981 CAS No. 1628478-15-8

trans-isrib A17 (ISR-IN-1) is an potent inhibitor of the integrated stress response with EC50 of 0.6 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 74 In Stock
5MG 69 In Stock
10MG 103 In Stock
25MG 211 In Stock
50MG 305 In Stock
100MG 436 In Stock
200MG 629 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    trans-isrib A17
  • Note
    Research use only, not for human use.
  • Brief Description
    trans-isrib A17 (ISR-IN-1) is an potent inhibitor of the integrated stress response with EC50 of 0.6 nM.
  • Description
    ISR-IN-1 (Compound 48) is an inhibitor of the integrated stress response (EC50: 0.6 nM).
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1628478-15-8
  • Formula Weight
    487.32
  • Molecular Formula
    C22H22Cl2F2N2O4
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 12.5 mg/mL (25.65 mM; Ultrasonic )
  • SMILES
    O(CC(N[C@H]1CC[C@H](NC(COC2=CC(F)=C(Cl)C=C2)=O)CC1)=O)C3=CC(F)=C(Cl)C=C3
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Hearn BR, et al. Structure-Activity Studies of Bis-O-Arylglycolamides: Inhibitors of the Integrated Stress Response. ChemMedChem. 2016 Apr 19;11(8):870-80. ?
molnova catalog
related products
  • CGP52411

    CGP52411 (DAPH) is a highly selective, orally active, and ATP-competitive EGFR inhibitor (IC50: 0.3 μM).

  • (3beta,20xi,21S,23S,...

    (3beta,20xi,21S,23S,24E)-20,21,26-trihydroxy-19-oxo-21,23-epoxydammar-24-en-3-yl 6-deoxy-alpha-L-mannopyranosyl-(1->2)-[beta-D-xylopyranosyl-(1->3)]-alpha-L-arabinopyranoside

  • TH-263

    TH-263 is inactive toward both LIMK1 and LIMK2 and thus can be used as negative control for TH-257, and is a diaryl sulfonamide derivative.