半胱胺盐酸盐 T6460
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 |
---|---|---|---|
500 mg | 156-57-0 | ¥333.00 | 询底价 |
1 mL | 156-57-0 | ¥418.00 | 询底价 |
5 g | 156-57-0 | ¥418.00 | 询底价 |
Product Introduction
Bioactivity
英文名: Cysteamine hydrochloride
描述: Cysteamine hydrochloride (Thioethanolamine Hydrochloride) 是一种可口服的,用于肾病型胱胺酸症的小分子药物,也可作为抗氧化剂。
体外活性: Cysteamine has been shown to increase intracellular glutathione levels in cystinotic cells, thus restoring the altered redox state of the cells. Also increased rates of apoptosis in cystinotic cells, which are thought to be the result of increased caspase 3 and protein kinase Cε activity, is counteracted by Cysteamine administration. Cysteamine has antioxidant properties as a result of increasing glutathione production. Cysteamine is an excellent scavenger of OH and HOCl; it also reacts with Water2. Cysteamine increases the production of several heat shock proteins (HSP), including the murine Hsp40. Cysteamine exerts a dose-dependent effect on the doxorubicin-induced death of cancer cells, measured in both HeLa cells and B16 cells, whereas Cysteamine treatment alone had no influence on cell survival. In addition, in a doxorubicin-resistant breast cancer cell line, the addition of Cysteamine to doxorubicin results in a dramatic increase in cell death. [1] Cysteamine (100 μM) significantly is able to increase the intracellular GSH levels and the percentage of embryos that developed to the blastocyst stage of culture matured oocytes. [2]
体内活性: Cysteamine is introduced as a treatment for cystinosis by depleting lysosomal cystine. Cystamine can inhibit transglutaminase activity by binding to the cysteine in its active center. Cysteamine increases brain levels of brain-derived neurotrophic factor (BDNF), which is caused by the increased expression of the heat shock DNAJ-containing protein 1 (HSJ1). Cysteamine inhibits the formation of gastric and mammary tumors that are induced chemically or after irradiation, respectively. The administration of Cysteamine is also able to inhibit the metastasis of pancreatic cancer in a mouse model by decreasing the expression and activity of metalloproteinases. [1]
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: Ethanol : 22 mg/mL (193.6 mM)
H2O : 21 mg/mL (184.8 mM)
DMSO : 60 mg/mL (528.12 mM)
关键字: cystinosis | b-Mercaptoethylamine Hydrochloride | antioxidant | 2-Aminoethanethiol | nephropathic | Autophagy | Apoptosis | Inhibitor | Reactive Oxygen Species | Cysteamine | Cysteamine hydrochloride | Endogenous Metabolite | inhibit | Cysteamine Hydrochloride | beta-Mercaptoethylamine Hydrochloride | orally | 2-Mercaptoethylamine
相关产品: Demethylzeylasteral | Tafasitamab | Crebanine | Inecalcitol | Telomerase-IN-4 | 5'-Amino-5'-deoxyadenosine | Neogambogic acid | Sclareol | Curzerene | Diatrizoic Acid
相关库: Anti-Tumor Natural Product Library | Drug Repurposing Compound Library | Human Endogenous Metabolite Library | Anti-Prostate Cancer Compound Library | FDA-Approved & Pharmacopeia Drug Library | Anti-Cancer Drug Library | Human Metabolite Library | Anti-Cancer Approved Drug Library | Anti-Fibrosis Compound Library | Autophagy Compound 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