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Lixisenatide是一种胰高血糖素样肽-1(GLP-1)受体激动剂,主要通过激活GLP-1信号通路调节血糖稳态。除降糖作用外,Lixisenatide还可通过下调促炎细胞因子表达抑制炎症反应,并影响Akt-MEK1/2等信号通路,同时减轻氧化应激、线粒体功能障碍及细胞凋亡,在代谢性疾病及炎症相关疾病(如糖尿病及其并发症)等研究中具有潜在应用价值。
别名 利西拉肽
Lixisenatide是一种胰高血糖素样肽-1(GLP-1)受体激动剂,主要通过激活GLP-1信号通路调节血糖稳态。除降糖作用外,Lixisenatide还可通过下调促炎细胞因子表达抑制炎症反应,并影响Akt-MEK1/2等信号通路,同时减轻氧化应激、线粒体功能障碍及细胞凋亡,在代谢性疾病及炎症相关疾病(如糖尿病及其并发症)等研究中具有潜在应用价值。

| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 619 | 现货 | |
| 5 mg | ¥ 2,099 | 现货 |
TargetMol的所有产品仅用作科学研究或药证申报,不能被用于人体,我们不向个人提供产品和服务。请您遵守承诺用途,不得违反法律法规规定用于任何其他用途。
| 产品描述 | Lixisenatide is a glucagon-like peptide-1 (GLP-1) receptor agonist that primarily regulates glucose homeostasis by activating the GLP-1 signaling pathway. Beyond its glucose-lowering effects, lixisenatide suppresses inflammatory responses by downregulating pro-inflammatory cytokine expression and modulates signaling pathways such as Akt-MEK1/2. Additionally, it alleviates oxidative stress, mitochondrial dysfunction, and apoptosis, demonstrating potential value in research on metabolic diseases and inflammation-related conditions (e.g., diabetes and its complications). |
| 别名 | 利西拉肽 |
| 分子量 | 4858.49 |
| 分子式 | C215H347N61O65S |
| CAS No. | 320367-13-3 |
| 密度 | no data available |
| Sequence | His-Gly-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Leu-Ser-Lys-Gln-Met-Glu-Glu-Glu-Ala-Val-Arg-Leu-Phe-Ile-Glu-Trp-Leu-Lys-Asn-Gly-Gly-Pro-Ser-Ser-Gly-Ala-Pro-Pro-Ser-Lys-Lys-Lys-Lys-Lys-Lys-NH₂ |
| Sequence Short | HGEGTFTSDLSKQMEEEAVRLFIEWLKNGGPSSGAPPSKKKKKK |
| 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. 实际储存温度请以COA为准 | ||||||||||||||||||||
| 溶解度信息 | H2O: 80 mg/mL (16.47 mM), Sonication and heating are recommended. | ||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||
H2O
该溶液配制表仅适用于固体产品。对于液体产品,请根据标明的浓度或密度计算稀释方案。 | |||||||||||||||||||||
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