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| Product | Description | |
|---|---|---|
| Pracinostat | Pracinostat is a potent and orally active histone deacetylase (HDAC) inhibitor with high tumor exposure and efficacy in mouse models of colorectal cancer. The selectivity of Pracinostat for tumor tissues makes it a promising therapeutic candidate for use in patients with advanced solid malignancies. Group: Biochemicals. Alternative Names: (2E)-3-[2-Butyl-1-[2-(diethylamino)ethyl]-1H-benzimidazol-5-yl]-N-hydroxyacrylamide; (E)-3-[2-Butyl-1-(2-diethylaminoethyl)-1H-benzimidazol-5-yl]-N-hydroxy-2-propenamide; Kaempferol 3-O- β-D-(6-E-p-Coumaroylglucoside); SB 939; SB939; (2E)-3-[2-Butyl-1-[2-(diethylamino)ethyl]-1H-benzimidazol-5-yl]-N-hydroxy-2-propenamide. Grades: Highly Purified. CAS No. 929016-96-6. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| Pracinostat | Pracinostat is a potent histone deacetylase (HDAC) inhibitor, with IC50s of 40-140 nM, used for cancer research. Pracinostat also inhibits metallo-?-lactamase domain-containing protein 2 (MBLAC2) hydrolase activity with an EC50 below 10 nM[1][4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SB939. CAS No. 929016-96-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13322. |  |
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