Terlipressin Acetate
商品编号:
TS0488
备注:
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详细介绍
l 基本信息 |
产品名称 | Terlipressin Acetate |
一般描述 | Terlipressin Acetate is an analogue of vasopressin used as a vasoactive drug in the management of hypotension. It has been found to be effective when norepinephrine does not help. |
别 称 | Gly-Gly-Gly-Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Lys-Gly-NH2(Cys4-Cys9) |
纯 度 | ≥98.0% (HPLC) | CAS NO. | 14636-12-5 |
分子式 | C52H74N16O15S2
· xC2H4O2 | 分子量 | 1227.37 (free base basis) |
适用范围 | 生物试剂,适用于细胞培养等 |
l 理化信息 |
外 观 | 白色粉末 |
溶解性(25°C) | 水 | Very slight soluble |
l 生物学信息 |
生物活性/药理作用 | Terlipressin is a synthetic triglycyllysine derivative of vasopressin with vasoconstrictive, antihemorrhagic, and antidiuretic properties. Upon intravenous administration, terlipressin, an inactive prodrug, is biotransformed to its active moiety, lysine vasopressin
(LVP), a nive vasopressin analogue with affinity for vasopressin receptors V1 (V1a), V2 and V3 (V1b). As a V1 agonist, terlipressin increases systemic vascular resistance, particularly in the splanchnic area, resulting
in a decrease of portal pressure. V1 binding also promotes platelet aggregation and glycogenolysis, while V3 binding induces adrenocorticotropic hormone (ACTH) secretion. Compared to vasopressin, terlipressin has a minimal effect on V2 receptors, which are responsible for promotion of water reabsorption in the collecting ducts of the kidney via stimulation of cyclic AMP production. |
l 存储 |
存储温度 | -20°C |
l 注意事项及免责声明 |
本产品仅用于实验研究,不得作为药物使用,不得用于家用或其它用途。 |
l 参考文献 |
1. http://www.drugbank.ca 2. https://ncit.nci.nih.gov 3. https://www.ncbi.nlm.nih.gov |