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Merck
CN
所有图片(1)

主要文件

681671

Sigma-Aldrich

IWP-2

≥97% (HPLC), solid, Wnt antagonist, Calbiochem

别名:

Wnt拮抗剂II,IWP-2, Wnt 生P产抑制剂-2,Wnt通路抑制剂II,Porcn抑制剂I

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About This Item

经验公式(希尔记法):
C22H18N4O2S3
分子量:
466.60
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77

产品名称

Wnt拮抗剂II,IWP-2, The Wnt Antagonist II, IWP-2, also referenced under CAS 686770-61-6, controls the biological activity of Wnt. This small molecule/inhibitor is primarily used for Cancer applications.

质量水平

方案

≥97% (HPLC)

表单

solid

制造商/商品名称

Calbiochem®

储存条件

OK to freeze
protect from light

颜色

off-white

溶解性

DMSO: 2.5 mg/mL

运输

ambient

储存温度

2-8°C

SMILES字符串

[s]1c2c(nc1NC(=O)CSc3[n]([c](c5c(n3)CCS5)=O)c4ccccc4)ccc(c2)C

InChI

1S/C22H18N4O2S3/c1-13-7-8-15-17(11-13)31-21(23-15)25-18(27)12-30-22-24-16-9-10-29-19(16)20(28)26(22)14-5-3-2-4-6-14/h2-8,11H,9-10,12H2,1H3,(H,23,25,27)

InChI key

WRKPZSMRWPJJDH-UHFFFAOYSA-N

一般描述

一种细胞渗透性苯并噻唑基乙酰胺化合物,通过选择性阻断MBOAT(膜结合O-酰基转移酶)家族成员Porcn-(Porcupine)介导的Wnt棕榈酰化作用抑制细胞Wnt加工和分泌。IWP-2一般不影响Wnt/β-连环蛋白信号通路,与IWR-1-endo(目录号681669)不同,IWP-2对Wnt刺激的细胞反应没有影响。也可以10 mM的DMSO溶液(目录号506072)提供。
一种细胞渗透性苯并噻唑基乙酰胺化合物,通过选择性阻断MBOAT(膜结合O-酰基转移酶)家族成员Porcn-(Porcupine)介导的Wnt棕榈酰化作用抑制细胞Wnt加工和分泌。IWP-2一般不影响Wnt/β-连环蛋白信号通路,与IWR-1-endo(目录号681669)不同,IWP-2对Wnt刺激的细胞反应没有影响。

包装

用惰性气体包装

警告

毒性:有害(C)

重悬

复溶后,等分并冷冻保存(-20°C)。贮备溶液在-20°C下可稳定保存至多3个月。

其他说明

Chen, B., et al. 2009.Nature Chem. Biol.5, 100.

法律信息

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

储存分类代码

11 - Combustible Solids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Generation of cardiomyocytes from human pluripotent stem cells (hPSCs) is of high interest for disease modelling and regenerative medicine. hPSCs can provide an unlimited source of patient-specific cardiomyocytes that are otherwise difficult to obtain from individuals. Moreover, the low proliferation
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Journal of pain research, 13, 1049-1058 (2020-06-18)
The upregulation of spinal NMDA receptor is a crucial mechanism in remifentanil-induced hyperalgesia (RIH). Wnt3a/β-catenin pathway plays an important role in neuropathic pain. We hypothesized that wnt3a inhibitor (iwp-2) could downregulate the expression of NR2B subunit in NMDA receptor, in
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