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
  • EPZ020411 dihydrochl...

    EPZ020411 is a potent, selective PRMT6 inhibitor with IC50 of 10 nM, displays 10-fold and 20-fold selectivity over PRMT1/8.

  • PR5-LL-CM01

    PR5-LL-CM01 is a novel selective, small-molecule inhibitor of PRMT5 methyltransferase with IC50 of 7.5 uM.

  • UNC0379

    UNC0379 is a selective, substrate-competitive inhibitor of lysine methyltransferase SETD8 with IC50 of 7.3 uM.