Description |
Campathecin is a potent DNA enzyme topoisomerase I inhibitor, with an IC50 of 679 nM.
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Target |
Topoisomerase I:679 nM (IC50)
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In Vitro |
[3H]BrCPT labeling of topoisomerase I is enhanced greatly by the presence of DNA; very little labeling of isolated topoisomerase I or isolated DNA occurrs. Even in the presence of DNA, [3H]BrCPT labeling of topoisomerase I is inhibited by camptothecin, suggesting that both CPT and BrCPT bind to the same site on the DNA-topoisomerase I binary complex[1]. With increasing concentrations of camptothecin, closed circular pRR322 DNA (form I) is converted to nicked circular DNA (form 11). This apparent nicking activitv of camptothecin required DNA topoisomerase I[2].
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Density | 1.5±0.1 g/cm3 |
Boiling Point | 757.0±60.0 °C at 760 mmHg |
Flash Point | 411.6±32.9 °C |
Exact Mass | 348.110992 |
PSA | 81.42000 |
LogP | 1.60 |
Vapour Pressure | 0.0±2.7 mmHg at 25°C |