中文名 | CVT-313 |
英文名 | CVT-313 |
别名 | 化合物CVT313 CVT-313游离态 CDK2抑制剂(CVT-313) 2,2'-((9-异丙基-6-((4-甲氧基苄基)氨基)-9H-嘌呤-2-基)氮烷二基)二乙醇 |
英文别名 | BAT5 D6S82E CVT-313 CVT 313 CVT-313(NG-26) CDK2 INHIBITOR III Anti-ABHD16A antibody produced in rabbit 2(BIS-(HYDROXYETHYL)AMINO)-6-(4-METHOXYBENZYLAMINO)-9-ISOPROPYL-PURINE 2,2'-(9-isopropyl-6-(4-methoxybenzylamino)-9H-purin-2-ylazanediyl)diethanol |
CAS | 199986-75-9 |
化学式 | C20H28N6O3 |
分子量 | 400.47 |
InChIKey | NQVIIUBWMBHLOZ-UHFFFAOYSA-N |
密度 | 1.30±0.1 g/cm3(Predicted) |
沸点 | 652.3±65.0 °C(Predicted) |
酸度系数 | 13.95±0.10(Predicted) |
存储条件 | Sealed in dry,Store in freezer, under -20°C |
外观 | 白色固体 |
体外研究 | CVT-313 (Cdk2 Inhibitor III) has been shown to inhibit other kinases, but at much higher IC 50 values, i.e., CDK1 (IC 50 =4.2 μM), CDK4 D1 (IC 50 =215 μM), and MAPK/PKA/PKC (IC 50 >1.25 mM), compared to CDK2 (IC 50 =0.5 μM). CVT-313 has been shown to have profound effects on cell proliferation at concentrations of 5-20 μM. CVT-313 is a potent CDK2 inhibitor, which is identified from a purine analog library with an IC 50 of 0.5 μM in vitro. Inhibition is competitive with respect to ATP (K i =95 nM), and selective CVT-313 has no effect on other, nonrelated ATP-dependent serine/threonine kinases. When added to CDK1 or CDK4, a 8.5- and 430-fold higher concentration of CVT-313 is required for half-maximal inhibition of the enzyme activity. Using normal and tumor human/murine cell lines, the effects of CVT-313 on cell proliferation is measured. The IC 50 for growth inhibition ranged from 1.25 to 20 μM. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.497 ml | 12.485 ml | 24.971 ml |
5 mM | 0.499 ml | 2.497 ml | 4.994 ml |
10 mM | 0.25 ml | 1.249 ml | 2.497 ml |
5 mM | 0.05 ml | 0.25 ml | 0.499 ml |
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