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Merck
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重要文件

SML0203

Sigma-Aldrich

iCRT14

≥98% (HPLC)

同義詞:

5-[[2,5-二甲基-1-(3-吡啶基)-1H-吡咯-3-基]亚甲基]-3-苯基-2,4-噻唑烷二酮

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About This Item

經驗公式(希爾表示法):
C21H17N3O2S
CAS號碼:
分子量::
375.44
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

品質等級

化驗

≥98% (HPLC)

形狀

powder

顏色

yellow to orange

溶解度

DMSO: ≥10 mg/mL

儲存溫度

2-8°C

SMILES 字串

Cc1cc(\C=C2/SC(=O)N(c3ccccc3)C2=O)c(C)n1-c4cccnc4

InChI

1S/C21H17N3O2S/c1-14-11-16(15(2)23(14)18-9-6-10-22-13-18)12-19-20(25)24(21(26)27-19)17-7-4-3-5-8-17/h3-13H,1-2H3/b19-12-

InChI 密鑰

NCSHZXNGQYSKLR-UNOMPAQXSA-N

應用

iCRT14可用于Wnt /β-连环蛋白介导的细胞信号转导研究。

生化/生理作用

iCRT14属于噻唑烷二酮类β-连环蛋白反应性转录抑制剂。它可降低散乱蛋白的水平并调节T细胞因子(TCF)与DNA的结合。 它会导致结肠癌细胞中细胞增殖和肿瘤生长减少的持续减弱。
iCRT14是一种Wnt / β-连环蛋白途径抑制剂。它是连环蛋白应答转录(CRT)报告基因的有效抑制剂,以及内源基因靶标。iCRT14还可以剂量依赖性方式破坏β-连环蛋白-TCF4的相互作用,并在结肠肿瘤细胞系中引起G0/G1 的停滞。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Daiana S Sánchez et al.
Biochemical and biophysical research communications, 512(2), 170-175 (2019-03-19)
This work was aimed to determine the effect of 17β-estradiol (17βE) on cell proliferation in human renal tubular epithelial cells (HRTEC) isolated from kidneys from pediatric subjects, as well as the role of estrogen receptors involved in the 17βE proliferative
The S-G2 phase enriched beta-catenin/TCF complex ensures cell survival and cell cycle progression
Ding Y, et al.
Journal of Cell Science, jcs-146977 (2014)
Winning WNT: race to Wnt signaling inhibitors.
Kazuhide Watanabe et al.
Proceedings of the National Academy of Sciences of the United States of America, 108(15), 5929-5930 (2011-04-01)
Xin Wang et al.
Nature communications, 7, 10633-10633 (2016-02-05)
Cancer stem cells (CSCs) contribute to tumour heterogeneity, therapy resistance and metastasis. However, the regulatory mechanisms of cancer cell stemness remain elusive. Here we identify PCNA-associated factor (PAF) as a key molecule that controls cancer cell stemness. PAF is highly
Caihong Wang et al.
Oncoimmunology, 9(1), 1809947-1809947 (2020-09-18)
In colorectal cancer, Wnt/β-catenin signaling is often aberrantly activated and associated with a T-cell-excluded phenotype which is a major obstacle for many immunotherapies. However, the effects of Wnt/β-catenin inhibition on tumor immunity and immunotherapy remain to be elucidated. In syngeneic

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