GSK3326595

CAS No. 1616392-22-3

GSK3326595 ( GSK-3326595;EPZ015938;EPZ-015938 )

Catalog No. M12361 CAS No. 1616392-22-3

A potent, selective, reversible and orally active PRMT5 inhibitor with IC50 of 22 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 35 In Stock
10MG 50 In Stock
25MG 98 In Stock
50MG 177 In Stock
100MG 332 In Stock
200MG 440 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    GSK3326595
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, selective, reversible and orally active PRMT5 inhibitor with IC50 of 22 nM.
  • Description
    A potent, selective, reversible and orally active PRMT5 inhibitor with IC50 of 22 nM; potently inhibits tumor growth in cellular and animal models.Blood Cancer Phase 1 Clinical
  • Synonyms
    GSK-3326595;EPZ015938;EPZ-015938
  • Pathway
    Chromatin/Epigenetic
  • Target
    HMTase
  • Recptor
    HMTase
  • Research Area
    Cancer
  • Indication
    Blood cancer

Chemical Information

  • CAS Number
    1616392-22-3
  • Formula Weight
    452.55
  • Molecular Formula
    C24H32N6O3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 30 mg/mL
  • SMILES
    O=C(C)N1CCC(NC2=NC=NC(C(NC[C@H](O)CN3CCC(C=CC=C4)=C4C3)=O)=C2)CC1
  • Chemical Name
    4-Pyrimidinecarboxamide, 6-[(1-acetyl-4-piperidinyl)amino]-N-[(2S)-3-(3,4-dihydro-2(1H)-isoquinolinyl)-2-hydroxypropyl]-

Shipping & Storage Information

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

Reference

1. Drew Rasco, et al. Abstract CT038, AACR. DOI: 10.1158/1538-7445.
2. Patent WO 2016022605 A1, Formula A.
molnova catalog
related products
  • UNC3866

    A potent, selective PRC1 chromodomains antagonist that binds to CBX4 and CBX7 with Kd of 100 nM.

  • UNC0638

    A potent, selective, substrate-competitive inhibitor of G9a (EHMT2) and GLP (EHMT1) with IC50 of <15 nM and 19 nM in SAHH-coupled assays, respectively.

  • WDR5-MLL1 inhibitor

    WDR5-MLL1 inhibitor is a novel potent inhibitor of WDR5-MLL1 interaction, binds to WDR5 with Kd of 1 nM.