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Merck
CN

I0161

IWR-1

≥98% (HPLC), powder, Tankyrase1/2 inhibitor

别名:

4-(1,3,3a,4,7,7a-六氢-1,3-二氧代-4,7-亚甲基-2H-异吲哚-2-基)-N-8-喹啉基-苯甲酰胺, IWR1

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关于此项目

经验公式(希尔记法):
C25H19N3O3
化学文摘社编号:
分子量:
409.44
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
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产品名称

IWR-1, ≥98% (HPLC)

SMILES string

O=C(Nc1cccc2cccnc12)c3ccc(cc3)N4C(=O)[C@@H]5[C@H]6C[C@H](C=C6)[C@@H]5C4=O

InChI

1S/C25H19N3O3/c29-23(27-19-5-1-3-14-4-2-12-26-22(14)19)15-8-10-18(11-9-15)28-24(30)20-16-6-7-17(13-16)21(20)25(28)31/h1-12,16-17,20-21H,13H2,(H,27,29)/t16-,17+,20-,21+

InChI key

ZGSXEXBYLJIOGF-ALFLXDJESA-N

assay

≥98% (HPLC)

color

white to beige

solubility

DMSO: 5 mg/mL, clear

storage temp.

room temp

Quality Level

Application

IWR-1已被用作人类胚胎干细胞(hESCs)、小鼠lewis肺癌(LLC)和Sepia胚胎中Wingless/Integrated(WNT)信号通路的拮抗剂。

Biochem/physiol Actions

IWR-1是一种端锚聚合酶抑制剂,其对癌症干细胞样细胞具有细胞毒性。它可抑制 体内 骨肉瘤的进展。IWR-1可与RNA聚合酶II相互作用,对于预启动复合物的形成至关重要。
Wnt/b-连环蛋白(‘经典′)途径维持转录程序,使干细胞保持多能性。
Wnt/b-连环蛋白(‘经典′)途径维持转录程序,使干细胞保持多能性。Wnt/b-连环蛋白途径超活化会导致疾病分期。IWR-3充当Wnt反应的抑制剂。似乎IWR化合物通过直接相互作用诱导Axin蛋白稳定化,该蛋白是b-连环蛋白破坏复合体(由Apc、Axin、Ck1和Gsk3b组成)的一部分。

Features and Benefits

该化合物是基因调控研究的推荐产品。点击此处,了解更多推荐基因调控产品。了解更多有关用于其他研究领域的生物活性小分子的信息,请访问sigma.com/discover-bsm

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Iwr1 protein is important for preinitiation complex formation by all three nuclear RNA polymerases in Saccharomyces cerevisiae
Esberg A, et al.
PLoS ONE, 6(6), e20829-e20829 (2011)
Hirokazu Narita et al.
Scientific reports, 7(1), 13708-13708 (2017-10-24)
One of the major challenges in cell-based cardiac regenerative medicine is the in vitro construction of three-dimensional (3D) tissues consisting of induced pluripotent stem cell-derived cardiomyocyte (iPSC-CM) and a blood vascular network supplying nutrients and oxygen throughout the tissue after
Fei Gao et al.
Cancer letters, 402, 177-189 (2017-06-13)
Akt1 is essential for the oncogenic transformation and tumor growth in various cancers. However, the precise role of Akt1 in advanced cancers is conflicting. Using a neuroendocrine TRansgenic Adenocarcinoma of the Mouse Prostate (TRAMP) model, we first show that the
Efficient differentiation of TBX18+/WT1+ epicardial-like cells from human pluripotent stem cells using small molecular compounds
Zhao J, et al.
Stem Cells and Development, 26(7), 528-540 (2017)
A serine in exon 11 determines the full transcriptional activity of TCF-4 in lung carcinoma cells
Yang B, et al.
Biochemical and biophysical research communications, 508(3), 675-681 (2019)

商品

We offer a variety of small molecule research tools, such as transcription factor modulators, inhibitors of chromatin modifying enzymes, and agonists/antagonists for target identification and validation in gene regulation research; a selection of these research tools is shown below.

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