您好,欢迎来到化工原料网! [登录] [免费注册]
化工原料网
位置:首页 > 产品库 > A-1155463
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
A-1155463
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
A-1155463图片
CAS NO:1235034-55-5
规格:98%
分子量:669.79
包装与价格:
包装价格(元)
5mg电议
25mg电议

产品介绍
BCL-XL inhibitor, potent and selective
CAS:1235034-55-5
分子式:C35H32FN5O4S2
分子量:669.79
纯度:98%
存储:Store at -20°C

Background:

Ki=19 nM


A-1155463 is a potent and selective BCL-XL inhibitor.


BCL-2 plays a key role in the survival of lymphoid malignancies, while BCL-XL overexpression has been associated with drug resistance and disease progression of various solid tumors and hematological malignancies.


In vitro: A-1155463 was identified via nuclear magnetic resonance fragment screening and structure-based design to be a highly potent and selective BCL-XL inhibitor. A-1155463 was found to be substantially more potent against BCL-XL-dependent cell lines relative to the previously reported inhibitor, WEHI-539 [1].


In vivo: Animal study showed that following a single IP dose of A-1155463 at 5 mg/kg in nontumor bearing SCID-Beige mice, platelet counts dramatically decreased at 6 h postdose and then rebounded to normal levels within 72 h. Such platelet depletion and recovery kinetics were similar to those of the dual inhibitor navitoclax. Moreover, in order to give additional evidence that A-1155463 was conferring on-target in-vivo activity, A-1155463 was then administered to SCIDBeige mice that had been inoculated with BCL-XL-dependent H146 tumor cells. Results showed that the daily IP dosing of A-1155463 at 5 mg/kg for 14 days caused a statistically significant inhibition of tumor growth, which was alleviated upon cessation of dosing [1].


Clinical trial: Up to now, A-1155463 is still in the preclinical development stage.


Reference:
[1] Tao ZF et al.  Discovery of a Potent and Selective BCL-XL Inhibitor with in Vivo Activity. ACS Med Chem Lett. 2014 Aug 26;5(10):1088-93.