HSDVHK-NH2 是整合素 αvβ3-玻璃体结合蛋白的互作抑制剂,其IC50值为 1.74 pg/mL (2.414 pM)。
生物活性 | HSDVHK-NH2 is an antagonist of theintegrinαvβ3-vitronectininteraction, with anIC50of 1.74 pg/mL (2.414 pM)[1][2].
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体外研究 (In Vitro) | HSDVHK significantly inhibited bFGF-induced cell migration compared to the PBS control group[1]. The Arg-Gly-Asp (RGD)-binding site recognition by HSDVHK-NH2 (P11) is site specific because the HSDVHK-NH2 (P11) is inactive for the complex formation of a denatured form of integrin–vitronectin. HSDVHK-NH2 (P11) shows a strong antagonism against avb3-GRGDSP interaction with an IC50value of 25.72 nM[2]. HSDVHK-NH2 (P11) inhibits the HUVEC proliferation due to the induction of HUVEC cell death through caspases activations and its mechanism is related with increased p53 expression[3].
Cell Proliferation Assay[3] Cell Line: | HUVEC cells. | Concentration: | 0.1, 1, 10, and 100 μg/mL. | Incubation Time: | 72 h. | Result: | Significantly inhibited HUVEC proliferation on denatured collagen-coated plates in a dose-dependent manner. |
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Sequence Shortening | |
运输条件 | Room temperature in continental US; may vary elsewhere. |
储存方式 | Sealed storage, away from moisture and light Powder | -80°C | 2 years | | -20°C | 1 year |
*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light) |
溶解性数据 | In Vitro: H2O : 250 mg/mL(346.85 mM;Need ultrasonic) 配制储备液 1 mM | 1.3874 mL | 6.9369 mL | 13.8739 mL | 5 mM | 0.2775 mL | 1.3874 mL | 2.7748 mL | 10 mM | 0.1387 mL | 0.6937 mL | 1.3874 mL |
*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。 储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month (sealed storage, away from moisture and light)。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。 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 分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶 1. 请依序添加每种溶剂: PBS Solubility: 100 mg/mL (138.74 mM); Clear solution; Need ultrasonic
*以上所有助溶剂都可在本网站选购。 |