CAS NO: | 500577-51-5 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | Cyclo(-RGDfK) TFA is a potent and selective inhibitor of theαvβ3integrin, with anIC50of 0.94 nM[1]. Cyclo(-RGDfK) TFA potently targets tumor microvasculature andcancercells through the specific binding to the αvβ3integrinon the cell surface[3]. | ||||||||||||||||
IC50& Target |
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体外研究 (In Vitro) | Cyclo(-RGDfK) is a potent and selective inhibitor of the αvβ3integrin and exhibits aIC50of 0.94 nM[1].[66Ga]DOTA-E-[c(RGDfK)]2 can be prepared with high radiochemical purity (>97%), specific activity (36-67GBq/μM), in vitro stability, and moderate protein binding. MicroPET imaging up to 24 post-injection showed contrasting tumors reflecting αvβ3-targeted tracer accumulation[2]. | ||||||||||||||||
分子量 | 717.69 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C29H42F3N9O9 | ||||||||||||||||
CAS 号 | 500577-51-5 | ||||||||||||||||
Sequence Shortening | Cyclo(RGDFK) | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | Sealed storage, away from moisture
*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 100 mg/mL(139.34 mM;Need ultrasonic) H2O : 33.33 mg/mL(46.44 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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