Bufotaline
更新时间：2025-08-26 23:32:06
| 常用名 | 蟾毒它灵, 蟾蜍他灵 | CAS号 | 471-95-4 |
|---|---|---|---|
| 价格 | ￥需询单/1g | 纯度 | 98.0% |
| 备货期 | 1天 | 库存 | 现货 |
| 产品详情（用途，包装等）
用途： Bufotalin is a cardiotoxic bufanolide steroid, cardiac glycoside analogue, secreted by a number of toad species; a novel anti-osteoblastoma agent.IC50 value:Target:in vitro: bufotalin induced osteoblastoma cell death and apoptosis in dose- and time-dependent manners. Further, bufotalin induced endoplasmic reticulum (ER) stress activation in osteoblastoma cells, the latter was detected by the induction of C/EBP homologous protein (CHOP), phosphorylation of inositol-requiring enzyme 1 (IRE1) and PKR-like endoplasmic reticulum kinase (PERK), as well as caspase-12 activation [1]. Bufotalin was the most potent active compound among these four bufadienolides, and it exerted stronger inhibitory effect on the viability of doxorubicin-induced multidrug resistant liver cancer cells (R-HepG2) than that of their parent cells HepG2. bufotalin treatment induced cell cycle arrest at G(2)/M phase through down-regulation of Aurora A, CDC25, CDK1, cyclin A and cyclin B1, as well as up-regulation of p53 and p21. Bufotalin treatment also induced apoptosis which was accompanied by decrease in mitochondrial membrane potential, increases in intracellular calcium level and reactive oxygen species production, activations of caspase-9 and -3, cleavage of poly ADP-ribose polymerase (PARP) as well as changes in the expressions of bcl-2 and bax [2]. Bufotalin promoted death receptor-mediated cell death, especially TRAIL-induced apoptosis, through activation of caspase-3 and PARP-1. Cotreatment of bufotalin with TRAIL resulted in the downregulation of anti-apoptotic proteins, including Bcl-XL, Mcl-1, survivin and XIAP, and the up-regulation of MAPKs and TRAIL receptor DR5. In addition, phosphorylation of STAT1 was strongly inhibited by bufotalin [3]. externalization of phosphatidylserine, accumulation of sub-G(1) cells, fragmentation of DNA, and formation of apoptotic bodies were observed in bufotalin-treated Hep 3B cells [4]. 物理化学性质： CAS号：471-95-4 常用中文名：蟾毒它灵, 蟾蜍他灵 常用英文名：Bufotaline 分子式：C26H36O6 分子量：444.560 密度：1.3±0.1 g/cm3 沸点：591.7±50.0 °C at 760 mmHg 熔点：223°C (rough estimate) 闪点：195.8±23.6 °C 储存条件：库房通风低温干燥 |
- 上海化源生化科技有限公司
- 上海市 上海市 普陀区
- 产品名：蟾毒它灵
- 价格：
- 纯度：98.0%
- 备货期：10天
- 联系人：徐经理
- 上海吉至生化科技有限公司
- 上海市 上海市 奉贤区
- 产品名：蟾毒它灵
- 价格： ￥1178.0/20mg
- 纯度：98.0%
- 备货期：1天
- 联系人：刘佳
- 上海脉铂医药科技有限公司
- 上海市 上海市 嘉定区
- 产品名：蟾蜍他灵；蟾蜍皂素
- 价格： ￥1100.0/1g
- 纯度：98.0%
- 备货期：2天
- 联系人：李先生
- 上海阿拉丁生化科技股份有限公司
- 上海市 上海市 浦东新区
- 产品名：Bufotaline
- 价格： ￥3501.9/25mg ￥804.9/5mg ￥需询单/1g ￥需询单/1g
- 纯度：99.0%
- 备货期：1天
- 联系人：阿拉丁
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参考价格：$119/10mM*1mLinDMSO