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CUDC-907 | PI3K and HDAC inhibitor

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Price:
$159.00
Catalog #:
C2907-2s
Quantity:


Product Description

CUDC-907 is a orally-available, synergistic dual inhibitor of class I PI3K enzymes and class I and II HDAC enzymes. Its inhibition profile against PI3Ka, PI3Kb, and PI3Kd, is 19, 54, and 39 nM, respectively, while HDAC activity is 1.7, 5.0, 1.8, 27, and2.8 nM for HDAC1, HDAC2, HDAC3, HDAC6, and HDAC10, respectively. [1]

Through its dual action activity, CUDC-907 durably inhibits the PI3K-AKT-mTOR pathway and compensatory signaling molecules such as RAF, MEK, MAPK, and STAT3. In H1975 NSCLC cells and BT-474 cells, CUDC-907 was shown to reduce both phosphorylated and total protein levels of MET/EGFR, and HER2/3, respectively. [2] The integration of HDAC inhibition to a PI3K agent is thought to prevent the developmeng of drug resistance. CUDC-907 induces apoptosis and G2-M cell cycle arrest, and also induces caspase-3 and -7 activation in HCT-116 colon cancer cells in a dose-dependent manner.


Technical information:

Chemical Formula:   C23H24N8O4S
CAS #:   1339928-25-4
Molecular Weight:   508.55
Purity:   > 98%
Appearance:   White
Chemical Name:   N-hydroxy-2-(((2-(6-methoxypyridin-3-yl)-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methyl)(methyl)amino)pyrimidine-5-carboxamide
Solubility:   Up to 22 mM in DMSO
Synonyms:   CUDC-907, CUDC 907, CUDC907

Shipping Condition: The product is shipped in a glass vial at ambient temperature.
Storage condition: For longer shelf life, store solid powder at 4oC desiccated, or store DMSO solution at -20oC.


Reference:

1. Bao et al., Antitumor Activity of CUDC-907, a Single Small Molecule Inhibitor That Targets Both Pi3K and HDAC, in Hematologic Cancer Models. EORTC-AACR meeting poster, 2011.
2. Qian et al., Cancer network disruption by a single molecule inhibitor targeting both histone deacetylase activity and phosphatidylinositol 3-kinase signaling. Clin. Cancer Res. 2012, 18, 4104-4113. Pubmed ID: 22693356

Other Information:

Product Specification (pdf)
MSDS (pdf)
Certificate of Analysis is available upon request.

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