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| 产品名称 | Integrin ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Tirofiban | ✔ | 99%+ | |||||||||||||||||
| ATN-161 | ✔ | 98% | |||||||||||||||||
| RGD | ✔ | 98% | |||||||||||||||||
| A-205804 | ++ E-selectin, IC50: 20 nM ICAM-1, IC50: 25 nM | 98% | |||||||||||||||||
| SB-273005 | ++++ αvβ5 receptor, IC50: 0.3 nM αvβ3 receptor, IC50: 1.2 nM | 98+% | |||||||||||||||||
| Lifitegrast | ✔ | 97% | |||||||||||||||||
| Cilengitide TFA | +++ αvβ5 receptor, IC50: 79 nM αvβ3 receptor, IC50: 4.1 nM | 99%+ | |||||||||||||||||
| Cyclo(-RGDfK) TFA | ✔ | 99%+ | |||||||||||||||||
| Cyclo(RGDyK) trifluoroacetate | ++ αVβ3 integrin, IC50: 20 nM | 99%+ | |||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| 靶点 | 
 | 
| 描述 | Integrins are membrane-spanning heterodimers that mediate cell-extracellular matrix adhesion. Cyclo(-RGDfK) Trifluoroacetate is a potent and selective inhibitor of purified αvβ3 integrin with a KD value of 41.70 nM. In HEK293 (β3) cells, incubation with 2 μM Cyclo(-RGDfK) trifluoroacetate decreased the αvβ3 intergrin lateral mobility compared to the control group. When HEK293 (β3) cells were starved for 30 min and incubated with 1 μM Cyclo(-RGDfK) trifluoroacetate-Cy5 for 10 min at room temperature, the αvβ3 integrin internalization was less extensive than that in cells treated with regioselectively addressable functionalized template-arginine-alanine-aspartic acid (RAFT-RGD). Additionally, the internalization of αvβ3 integrin in HEK293 (β3) was dose-dependently induced by RAFT-RGD, and reached 79% increase versus control group at the dose of 1 μM. On the contrary, increasing doses of cyclo(-RGDfK) trifluoroacetate (0.1 - 4 μM) did not affect the integrin internalization as compared to the control cells[3]. In athymic mice bearing αvβ3-integrin-positive C6 gliomas, administration of cyclo(-RGDfK) trifluoroacetate conjugated to 177Lu-gold nanoparticles (2MBq/0.05 mL, four times from day 1 to 21) suppressed tumor progression, tumor metabolic activity, the number of intratumoral vessels and VEGF gene expression compared to mice treated with other radiopharmaceuticals[4]. | 
| Concentration | Treated Time | Description | References | |
| human podocytes | 1 μM | 24 h | Inhibited ITGB3 activity and alleviated podocyte injury | Cell Death Dis. 2019 May 24;10(6):401. | 
| human podocytes | 1 μM | 24 h | Inhibited ITGB3 activity and alleviated podocyte injury | Cell Death Dis. 2019 May 24;10(6):401. | 
| Administration | Dosage | Frequency | Description | References | ||
| Mice | Podocyte-specific miR-30 sponge transgenic mice | Intravenous injection | 10 mg/kg | Every 8 hours for a total of 3 times | Inhibited ITGB3 activity and alleviated proteinuria and podocyte injury | Cell Death Dis. 2019 May 24;10(6):401. | 
| Mice | Podocyte-specific miR-30 sponge transgenic mice | Intravenous injection | 10 mg/kg | Every 8 hours for a total of 3 times | Inhibited ITGB3 activity and alleviated proteinuria and podocyte injury | Cell Death Dis. 2019 May 24;10(6):401. | 
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 1.39mL 0.28mL 0.14mL | 6.97mL 1.39mL 0.70mL | 13.93mL 2.79mL 1.39mL | |
| CAS号 | 500577-51-5 | 
| 分子式 | C29H42F3N9O9 | 
| 分子量 | 717.69 | 
| SMILES Code | O=C(O)C(F)(F)F.O=C(O)C[C@@H](C(N[C@H](CC1=CC=CC=C1)C(N[C@@H](CCCCN)C(N[C@@H](CCCNC(N)=N)C(NC2)=O)=O)=O)=O)NC2=O | 
| MDL No. | MFCD20488083 | 
| 别名 | Cyclo | 
| 运输 | 蓝冰 | 
| InChI Key | WHCQIPJAWCYHFT-HXSCNMCGSA-N | 
| Pubchem ID | 91759592 | 
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, inert atmosphere, 2-8°C | 
| 溶解方案 | DMSO: 105 mg/mL(146.3 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO H2O: 30 mg/mL(41.8 mM),配合低频超声助溶 以下溶解方案都请先按照体外实验的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 
 
 
 
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