Bufotaline

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更新时间： 2025-08-26 23:32:06

CAS号：471-95-4

常用名： 蟾毒它灵, 蟾蜍他灵

价格：
￥需询单/1g

纯度： 98.0%

备货期： 1天

库存： 现货

其他详情（用途，包装）：
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

供应商信息：

公司名：武汉敬康恩生物医药科技有限公司推荐

认证状态： 已认证供应商

商品数： 5983件

电话： 15871494362

地址： 光谷大道58号

地区： 武汉市东西湖区

联系人： 周经理

联系人电话： 15871494362

邮件：orders@jknbiochem.com

网址：http://www.jknbiochem.com

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2024-09-29 价格：￥需询单蟾毒它灵

2022-02-19 价格：￥3501.9 Bufotaline

2025-12-29 价格：￥需询单蟾毒它灵

2019-03-05 价格：￥1178.0 蟾毒它灵

2024-07-15 价格：需询单蟾毒它灵

2016-10-29 价格：￥需询单蟾毒它灵

2022-10-13 价格：￥900.0 蟾毒它灵

2022-09-23 价格：￥1100.0 蟾蜍他灵；蟾蜍皂素

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蟾毒它灵, 蟾蜍他灵价格

Bufotaline

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