CAS NO: | 1681017-83-3 |
生物活性 | Venadaparib (IDX-1197) is a potent, selective and orally activePARPinhibitor withIC50s of 1.4 nM and 1.0 nM forPARP1andPARP2, respectively. Venadaparib does not sensitive to PARP-5. Venadaparib prevents the repair of DNA single-strand breaks (SSB) and can be used for solid tumors research[1][2]. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | In DNA damage-induced Hela cells, Venadaparib (IDX-1197) significantly inhibits PARP1-mediated PAR expression (EC50of 0.5 nM)[1]. | ||||||||||||||||
体内研究 (In Vivo) | In the germline BRCA1-mutated ovarian cancer PDX model, oral administration of Venadaparib (IDX-1197) exhibits significant PAR inhibition (>90%) in tumor tissues until 24 hr post dose. Venadaparib also dose-dependently led to potent tumor growth inhibition compared to Olaparib treatment group[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 406.45 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C23H23FN4O2 | ||||||||||||||||
CAS 号 | 1681017-83-3 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 100 mg/mL(246.03 mM;Need ultrasonic) 配制储备液
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