全部分类
  • Timosaponin A3
Timosaponin A3的可视化放大

Timosaponin A3

此产品仅用于科学研究,我们不为任何个人用途提供产品和服务

Timosaponin A3的二维码
可选规格
  • 包装
    价格
    促销价
    数量
  • 20mg
    ¥2455.00
    2209.00
    - +
已选 0 0
金额: ¥0.00
首页 收藏
Extracted from Anemarrhena asphodeloides Bge.;Store the product in sealed,cool and dry condition

货号:ajcn5474
CAS:41059-79-4
分子式:C39H64O13
分子量:740.43
纯度:98%
存储:Store at -20°C
库存:现货

Background:

Timosaponin AIII could inhibit acetylcholinesterase (AChE) activity, with an IC50 of 35.4 μM.


Timosaponin AIII could inhibit acetylcholinesterase (AChE) activity, with an IC50 of 35.4 μM[1]. Timosaponin AIII is identified as a major selective cytotoxic activity in BN108, and its selective cytotoxic activity involves inhibition of mTOR, induction of ER stress and protective autophagy[2].


Of the tested steroidal saponins, Timosaponin AIII (TA3) most potently improves memory deficits. Timosaponin AIII increases the scopolamine-induced reduction in step-through latency by 17% (10 mg/kg), 28% (20 mg/kg), and 43% (40 mg/kg). During the acquisition trial, no differences in latent time are observed. Timosaponin AIII (20, 40 mg/kg, p.o.) potently inhibits this reduction of acetylcholine in scopolamine-treated mouse brain. The inhibitory effect of Timosaponin AIII is comparable to that of tacrine, which is used as a positive control[1].


参考文献:
[1]. Lee B, et al. Timosaponin AIII, a saponin isolated from Anemarrhena asphodeloides, ameliorates learning and memory deficits in mice. Pharmacol Biochem Behav. 2009 Aug;93(2):121-7.
[2]. King FW, et al. Timosaponin AIII is preferentially cytotoxic to tumor cells through inhibition of mTOR and induction of ER stress. PLoS One. 2009 Sep 30;4(9):e7283.


没有评价数据

温馨提示 ×
商品已成功加入购物车!
购物车共 0 件商品
去购物车结算