GW-6604

  Cat. No.:  DC7980   Featured
Chemical Structure
452342-37-9
For research use only. We do not sell to patients.
We match the best price and quality on market.
Email:order@dcchemicals.com  sales@dcchemicals.com
Tel:+86-021-58447131
We are official vendor of:
  • 20
  • 19
  • 18
  • 17
  • 16
  • 15
  • 14
  • 12
  • 11
  • 10
  • 9
  • 8
  • 13
  • 6
  • 5
  • 4
  • 3
  • 2
  • 1
More than 5000 active chemicals with high quality for research!
Field of application
GW6604 is a potent and selective ALK-5 inhibitor with potent anticancer activity.
Cas No.: 452342-37-9
Chemical Name: GW-6604
SMILES: C1(C2=CC=CC=C2)=NC=CC(C3=CNN=C3C4=NC=CC=C4)=C1
Formula: C19H14N4
M.Wt: 298.34126
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: GW6604 is a potent and selective ALK-5 inhibitor with potent anticancer activity. GW6604 is also a TGF-beta signaling pathway inhibitor. In vitro, GW6604 inhibited autophosphorylation of ALK5 with an IC(50) of 140 nM and in a cellular assay inhibited TGF-beta-induced transcription of PAI-1 (IC(50): 500 nM). In vivo, GW6604 (40 mg kg(-1) p.o.) increased liver regeneration in TGF-beta-overexpressing mice, which had undergone partial hepatectomy. In an acute model of liver disease, GW6604 reduced by 80% the expression of collagen IA1. Inhibition of ALK5 could be an attractive new approach to treatment of liver fibrotic diseases by both preventing matrix deposition and promoting hepatocyte regeneration. (Br J Pharmacol. 2005 May;145(2):166-77.). (Last updated: 2/9/2015) For the detailed information of GW6604, the solubility of GW6604 in water, the solubility of GW6604 in DMSO, the solubility of GW6604 in PBS buffer, the animal experiment (test) of GW6604, the cell expriment (test) of GW6604, the in vivo, in vitro and clinical trial test of GW6604, the EC50, IC50,and affinity,of GW6604, Please contact DC Chemicals.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
Cat. No. Product name Field of application
DC41012 ALK2-IN-4 ALK2-IN-4 is a potent ALK2 inhibitor extracted from patent WO2020086963A1, compound Formula I free base.
DC8022 R-268712 Potent and selective inhibitor of the TGF-β type I receptor/ALK5 (IC50 = 2.5 nM). Exhibits ~ 5000-fold selectivity over p38 MAPK. Suppresses development of renal fibrosis in a unilateral ureteral obstruction model. Also reduces proteinuria, glomeruloscler
DC7980 GW-6604 GW6604 is a potent and selective ALK-5 inhibitor with potent anticancer activity.
X