200619-13-2 - Names and Identifiers
200619-13-2 - Physico-chemical Properties
Molecular Formula | C22H20N2O6
|
Molar Mass | 408.4 |
Solubility | DMSO : 50 mg/mL (122.43 mM; Need ultrasonic) |
Storage Condition | 2-8℃ |
In vitro study | DRF-1042 demonstrates superior lactone stability and good in vitro anticancer activity against a panel of human cancer cell lines including multi-drug resistance (MDR) phenotype. |
In vivo study | In clonogenic assay against murine, canine and human bone marrow cells, DRF-1042 treatment shows less mylosupression that supports the possibility of protracted dose schedule in both experimental and clinical studies. |
200619-13-2 - Preparation solution concentration reference
| 1mg | 5mg | 10mg |
---|
1 mM | 2.449 ml | 12.243 ml | 24.486 ml |
5 mM | 0.49 ml | 2.449 ml | 4.897 ml |
10 mM | 0.245 ml | 1.224 ml | 2.449 ml |
5 mM | 0.049 ml | 0.245 ml | 0.49 ml |
Last Update:2024-01-02 23:10:35
200619-13-2 - Reference Information
biological activity | DRF-1042 is an orally active camptothecin analog, it has the effect of inhibiting DNA topoisomerase I (DNA topoisomerase I). DRF-1042 showed good anticancer activity against a group of human cancer cell lines, including multidrug resistance (MDR) phenotypes. |
Target | DNA topoisomerase I |
Last Update:2024-04-09 19:05:17