| Name | drf-1042 | 
|---|---|
| Synonyms | 
                                
                                1H-Pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione, 4-ethyl-4-hydroxy-12-(2-hydroxyethoxy)-, (4S,12S)-
                                
                                
                                 (4S,12S)-4-Ethyl-4-hydroxy-12-(2-hydroxyethoxy)-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione 5-(2'-Hydroxyethoxy)-20(S)-camptothecin 1H-Pyrano(3',4':6,7)indolizino(1,2-b)quinoline-3,14(4H,12H)-dione,4-ethyl-4-hydroxy-12-(2-hydroxyethoxy)-,(4S) UNII-461WVF206P  | 
                        
| Description | DRF-1042 is an orally active camptothecin analog, which acts to inhibit DNA topoisomerase I. DRF-1042 shows good anticancer activity against a panel of human cancer cell lines[1][2]. | 
|---|---|
| Related Catalog | |
| References | 
| Density | 1.5±0.1 g/cm3 | 
|---|---|
| Boiling Point | 844.6±65.0 °C at 760 mmHg | 
| Molecular Formula | C22H20N2O6 | 
| Molecular Weight | 408.404 | 
| Flash Point | 464.6±34.3 °C | 
| Exact Mass | 408.132141 | 
| PSA | 110.88000 | 
| LogP | 0.60 | 
| Vapour Pressure | 0.0±3.3 mmHg at 25°C | 
| Index of Refraction | 1.726 |