Bioactivity | CT52923 is a selective, orally active platelet-derived growth factor receptor (PDGFR) antagonist. CT52923 also is an ATP-competitive inhibitor. CT52923 can be used for the research variety of pathological diseases, including atherosclerosis, glomerulonephritis, liver cirrhosis, pulmonary fibrosis, and cancer[1]. |
Invitro | CT52923 抑制 PDGFRs 和干细胞因子受体,IC50 值为 100 至 200 nM[1]。CT52923(0.01-30 μM;24 h)阻断血小板衍生生长因子诱导的平滑肌细胞迁移或成纤维细胞增殖,IC50 分别为 64 和 280 nM[1]。 Cell Migration Assay [1] Cell Line: |
In Vivo | CT52923(口服;5、15、30 和 50 mg/kg;每日两次)可显著抑制大鼠颈动脉损伤后内膜新生的形成[1]。 Animal Model: |
Name | CT52923 |
CAS | 205256-55-9 |
Formula | C23H25N5O4S |
Molar Mass | 467.54 |
Appearance | Solid |
Transport | Room temperature in continental US; may vary elsewhere. |
Storage | 4°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light) |
Reference | [1]. J C Yu, et al. Efficacy of the novel selective platelet-derived growth factor receptor antagonist CT52923 on cellular proliferation, migration, and suppression of neointima following vascular injury. J Pharmacol Exp Ther. 2001 Sep;298(3):1172-8. |