Description
CUDC-907 (Fimepinostat) is an inhibitor of PI3K and class I and II histone deacetylases (HDACs). This compound exhibits anticancer chemotherapeutic activity, inhibiting cell proliferation and tumor growth in a variety of cancer models.
Product Unit Size | Cost | Quantity | Stock |
---|
CUDC-907 (Fimepinostat) is an inhibitor of PI3K and class I and II histone deacetylases (HDACs). This compound exhibits anticancer chemotherapeutic activity, inhibiting cell proliferation and tumor growth in a variety of cancer models.
Cas No. | 1339928-25-4 |
---|---|
Purity | ≥98% |
Formula | C23H24N8O4S |
Formula Wt. | 508.55 |
Chemical Name | Fimepinostat |
IUPAC Name | N-hydroxy-2-[[2-(6-methoxypyridin-3-yl)-4-morpholin-4-ylthieno[3,2-d]pyrimidin-6-yl]methyl-methylamino]pyrimidine-5-carboxamide |
Synonym | Fimepinostat; CUDC 907; CUDC907 |
Solubility | DMSO 102 mg/mL (200.57 mM) Water Insoluble Ethanol Insoluble |
Appearance | White Crystal Powder |
Store Temp | -20°C |
---|---|
Ship Temp | Ambient |
MSDS | |
---|---|
Info Sheet |
Qian C, Lai CJ, Bao R, et al. Cancer network disruption by a single molecule inhibitor targeting both histone deacetylase activity and phosphatidylinositol 3-kinase signaling. Clin Cancer Res. 2012 Aug 1;18(15):4104-13. PMID: 22693356.
Prodrug
Mycotoxin produced by Fusarium fungi that infec...
Dibenzofuran produced by lichens.
Aminothiol, CoA component; ulcer inducer.
Diterpene component of vitamin A, differentiati...
Allosteric inhibitor
R-type Ca2+ and voltage-gated Na+ channel block...
FIASMA, 5-HT1/2, M1-5 mAChR, α1-adrenergic, hi...
Tricyclic antidepressant; potential D1/2 antago...
Carbapenem β-lactam; penicillin binding protei...
Fibrate; PPARα agonist.
Fluoroquinolone; topoisomerase IV, topoisomeras...
Endogenous APP peptide cleavage product, primar...
Akt inhibitor.
Trichothecene mycotoxin produced by Fusarium; p...
Laminin-derived nonapeptide.
Endogenous opioid peptide; μOR agonist.
BRD inhibitor.
Cannabinoid receptor 2 selective agonist.