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.
Protein synthesis inhibitor, DPP2 and metallope...
α1A-adrenergic antagonist.
HDAC inhibitor.
Dihydropyridine; L-type Ca2+ channel blocker.
Recombinant BNP, cardiomodulatory peptide; NPR-...
Fluoroquinolone; vacuolar H+ ATPase, topoisomer...
GRP analog, found in Bombina; bombesin and GRP ...
Tropane alkaloid found in Solanaceae plants; M1...
Curcumin derivative.
Fluoroquinolone; topoisomerase IV and bacterial...
MEK1/2 inhibitor.
Used for in vitro fertilization; FIASMA, SERM.<...
Taxane synthesis intermediate.
Macrolide; protein translation inhibitor, mamma...
Fluoroquinolone; bacterial DNA gyrase and helic...
ITC.
Methimazole prodrug; thyroid peroxidase inhibit...
AhR agonist.
Polyether cationic ionophore.
GSK3 and AChE inhibitor, potential σ1 agonist....