CAS NO: | 2229711-68-4 |
包装 | 价格(元) |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 | Vepdegestrant (ARV-471) is an oralestrogen receptorPROTAC protein degrader for breastcancer. Vepdegestrant is a hetero-bifunctional molecule that facilitates the interactions betweenestrogen receptoralpha and an intracellular E3 ligase complex. Vepdegestrant leads to the ubiquitylation and subsequent degradation of estrogen receptors via theproteasome. Vepdegestrant robustly degrades ER in ER-positive breastcancercell lines with a half-maximal degradation concentration (DC50) of ~2 nM[1]. | ||||||||||||||||
IC50& Target | Estrogen receptor[1] | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 723.90 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C45H49N5O4 | ||||||||||||||||
CAS 号 | 2229711-68-4 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | -20°C, sealed storage, away from moisture and light *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 110 mg/mL(151.95 mM;Need ultrasonic) 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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