Other grades of this product :
| CAY10603 Basic information |
| Product Name: | CAY10603 | | Synonyms: | CAY10603;Isox;tert-butyl 4-(3-((7-(hydroxyamino)-7-oxoheptyl)carbamoyl)isoxazol-5-yl)phenylcarbamate;HDAC6 Inhibitor;N-[4-[3-[[[7-(Hydroxyamino)-7-oxoheptyl]amino]carbonyl]-5-isoxazolyl]phenyl]carbamic acid 1,1-dimethylethyl ester;Histone Deacetylase Inhibitor VIII - CAS 1045792-66-2 - Calbiochem;CAY10603; CAY-10603; CAY 10603.;187257 | | CAS: | 1045792-66-2 | | MF: | C22H30N4O6 | | MW: | 446.5 | | EINECS: | | Product Categories: | Inhibitors | | Mol File: | 1045792-66-2.mol |
| CAY10603 Chemical Properties |
| density | 1.231±0.06 g/cm3(Predicted) | | storage temp. | +2C to +8C | | solubility | ≥22.35 mg/mL in DMSO; insoluble in EtOH; ≥24.85 mg/mL in H2O | | form | Beige to light brown solid | | pka | 9.47±0.20(Predicted) |
| CAY10603 Usage And Synthesis |
| Description | Histone deacetylase 6 (HDAC6) is a class II HDAC that represses transcription by removing acetyl groups from histones. In addition, HDAC6 deacetylases tubulin, which is important in regulating microtubule stability and function. CAY10603 is a potent and selective inhibitor of HDAC6 (IC50 = 0.002 nM, as compared with 271, 252, 0.42, 6851, and 90.7 nM for HDAC1, 2, 3, 8, and 10, respectively). Also, CAY10603 prevents the growth of several pancreatic cancer cell lines (IC50 = 0.1-1 μM). The HDAC6 inhibitor is more active in inhibiting cell growth than the broad spectrum HDAC inhibitor suberoylanilide hydroxamic acid (SAHA). | | General Description | A cell-permeable, active site Zn2+-targeting phenylisoxazolo-hydroxamate that acts a potent and highly selective HDAC6 inhibitor (IC50 = 0.002, 0.42, 90.7, 252, 271 and 6851 nM against HDAC-6, -3, -10, -2, -1 and -8, respectively). Shown to be more potent than SAHA in inhibiting the proliferation of a panel of pancreatic cancer cell lines (IC50<1.0 μM). |
| CAY10603 Preparation Products And Raw materials |
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