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别名 Ac-Arg-Aib-Arg-α(Me)Phe-NH2
Cenupatide is a urokinase plasminogen activator receptor (uPAR) inhibitor. Cenupatide inhibits uPAR binding to the formyl peptide receptors (FPRs) can improve kidney lesions in a rat model of STZ-induced diabetes. Cenupatide reverted STZ-induced up-regulation of uPA levels and activity, while uPAR on podocytes and (s)uPAR were unaffected. In glomeruli, Cenupatide inhibited FPR2 expression.

Cenupatide is a urokinase plasminogen activator receptor (uPAR) inhibitor. Cenupatide inhibits uPAR binding to the formyl peptide receptors (FPRs) can improve kidney lesions in a rat model of STZ-induced diabetes. Cenupatide reverted STZ-induced up-regulation of uPA levels and activity, while uPAR on podocytes and (s)uPAR were unaffected. In glomeruli, Cenupatide inhibited FPR2 expression.
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 5 mg | ¥ 1,467 | 5日内发货 | |
| 10 mg | ¥ 2,467 | 5日内发货 | |
| 25 mg | ¥ 4,467 | 5日内发货 | |
| 50 mg | ¥ 8,467 | 5日内发货 | |
| 100 mg | ¥ 14,467 | 5日内发货 | |
| 200 mg | ¥ 22,467 | 5日内发货 |
| 产品描述 | Cenupatide is a urokinase plasminogen activator receptor (uPAR) inhibitor. Cenupatide inhibits uPAR binding to the formyl peptide receptors (FPRs) can improve kidney lesions in a rat model of STZ-induced diabetes. Cenupatide reverted STZ-induced up-regulation of uPA levels and activity, while uPAR on podocytes and (s)uPAR were unaffected. In glomeruli, Cenupatide inhibited FPR2 expression. |
| 别名 | Ac-Arg-Aib-Arg-α(Me)Phe-NH2 |
| 分子量 | 617.756 |
| 分子式 | C28H47N11O5 |
| CAS No. | 1006388-38-0 |
| Smiles | CC(=O)N[C@@H](CCCNC(N)=N)C(=O)NC(C)(C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@](C)(Cc1ccccc1)C(N)=O |
| 密度 | 1.34 g/cm3 (Predicted) |
| Sequence | Ac-Arg-{Aib}-Arg-{aMePhe}-NH2 |
| Sequence Short | Ac-R-{Aib}-R-{aMePhe}-NH2 |
| 存储 | keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
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