醋酸特利加压素 T13920L
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
1 mg | 1884420-36-3 | ¥162.00 | 询底价 |
25 mg | 1884420-36-3 | ¥987.00 | 询底价 |
100 mg | 1884420-36-3 | ¥2,234.00 | 询底价 |
5 mg | 1884420-36-3 | ¥417.00 | 询底价 |
10 mg | 1884420-36-3 | ¥570.00 | 询底价 |
50 mg | 1884420-36-3 | ¥1,398.00 | 询底价 |
Product Introduction
Bioactivity
英文名: Terlipressin Acetate
描述: Terlipressin Acetate 是一种高度选择性的加压素 V1 受体激动剂,对氧和葡萄糖剥夺/再氧合 (OGD/R) 诱导的肠上皮细胞损伤 (IEC-6) 具有抗炎和抗氧化作用,可用于肝肾综合征和耐去甲肾上腺素的败血性休克的研究。
体外活性: Incubation with 25 nM terlipressin significantly improved cell viability, proliferation and apoptosis. Furthermore, terlipressin inhibited the secretion of TNF-α and 15-F2t-isoprostane from IEC-6 cells following OGD/R[1].
体内活性: Using a mouse nonlethal hepatic IR model, we found terlipressin administration significantly ameliorated IR-induced liver apoptosis, necrosis and inflammation[2].
存储条件: keep away from moisturePowder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 95mg/mL (70.50mM)
关键字: variceal | hepatorenal | vasoconstriction | Vasopressin Receptor | acute | anti-inflammatory | bleeding | anti-oxidative | Inhibitor | vasopressin | Terlipressin Acetate | Vasoconstrictor | Terlipressin | V1-receptors | inhibit
相关产品: d[Cha4]-AVP acetate(500170-27-4 free base) | Conopressin S acetate(111317-90-9 free base) | Vasopressin Dimer (parallel) (TFA) | Balovaptan | Tolvaptan | Desmopressin acetate (16679-58-6 free base) | Conivaptan hydrochloride | Desmopressin | Mozavaptan | Nelivaptan
相关库: Cyclic Peptide Library | Anti-Cancer Compound Library | Anti-Cancer Drug Library | Membrane Protein-targeted Compound Library | Macrocyclic Compound Library | Peptide Compound Library | Anti-Cancer Clinical Compound Library | Anti-Cancer Approved Drug Library | Preclinical Compound Library | Covalent Inhibitor Library
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途