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Windorphen
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。
Windorphen图片
CAS NO:19881-70-0
规格:98%
分子量:302.75
包装与价格:
包装价格(元)
5mg询价
25mg询价

Wnt inhibitor
CAS:19881-70-0
分子式:C17H15ClO3
分子量:302.75
纯度:98%
存储:Store at -20°C

Background:

Windorphen is a Wnt inhibitor that selectively abrogates the Wnt signaling for ventral development.


Wnt protein is a family of signaling proteins that interacts on the Wnt/β-Catenin pathways during embryotic development, cell proliferation, migration and adult tissue homeostasis.


In canonical Wnt/β-catenin reporter cell line STF293, Windorphen dose-dependently inhibits Wnt3a-inducible TOPFLASH-luciferase activity (IC50 of 1.5 mM). In human colon adenocarcinoma


SW480 cells with defective APC gene that constitutively activates Wnt signaling, 72 h treatment of Windorphen causes a wide spread apoptosis. [1]


In zebrafish embryos, Windorphen leads to apparent expansion of the dorsal markers (pax2.1) and marker of rhombomeres 3 and 5 at the six-somite stage (krox0). Windorphen selectively inhibits Wnt signaling in ventral and lateral regions of the 50% epiboly stage embryo (5.3 hpf). In addition, Windoprhen treatment rescues the telencephalon/eye phenotype in the mbl mutant zebrafish (i.e. a defective Axin1/β-catenin destruction complex causes abnormal activation of Wnt signaling and the loss of telencephalon and eyes.) [1]


Reference:
1.  Hao J, Ao A, Zhou L et al. Selective small molecule targeting β-catenin function discovered by in
vivo chemical genetic screen.  Cell Rep. 2013 Sep 12;4(5):898-904.


 
 
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