计算溶液所需的质量、体积或浓度。
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Information
Voreloxin hydrochloride (SNS-595, Vosaroxin) is a potentTopoisomerase IIinhibitor with broad-spectrum anti-tumor activity. Phase 2.
Targets
Topo II
In vitro
Voreloxin exhibits potent inhibitory effect in topoisomerase II relaxation with IC50 of 3.2 μg /mL without effect on topoisomerase II cleavage. Voreloxin has a cytotoxic activity against human tumor cell lines more potent than that of etoposide. Voreloxin has broad anti-proliferative activity in 15 cell lines, including 4 drug-resistant lines, with IC50 ranging from 0.04 to 1.155 μM.
In vivo
Voreloxin (50 mg/kg i.p.) shows potent in vivo antitumor activity mice implanted with P388 leukemia cells. Voreloxin (25 mg/kg i.v.) demonstrates strong tumor growth inhibition in 10 of 11 solid tumor (breast, ovarian, colon, lung, gastric, and melanoma) xenograft models, 2 hematologic tumor xenograft models, 3 multidrug resistant tumor models and 3 murine syngeneic tumor models (Colon 26, Lewis Lung carcinoma, M5076 Ovarian Sarcoma).
Cell Research(from reference)
Cell lines:P388 leukemia cells
Concentrations:~10 μg/mL
Incubation Time:72 hours
| ALogP | -1.138 |
|---|---|
| HBD Count | 1 |
| Rotatable Bond | 5 |
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| 批号(Lot Number) | 证书类型 | 货号 |
|---|---|---|
| 分析证书 | V422147 |