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SML0211

iCRT3

≥98% (HPLC), Wnt / b-catenin pathway inhibitor, powder

Sinonimo/i:

2-[[[2-(4-ethylphenyl)-5-methyl-4-oxazolyl]methyl]thio]-N-(2-phenylethyl)acetamide

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Voi/SKUDisponibilitàPrezzo
5 mg
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CHF 138.00
25 mg
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CHF 466.00

Informazioni su questo articolo

Formula empirica (notazione di Hill):
C23H26N2O2S
Numero CAS:
Peso molecolare:
394.53
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
MDL number:
Assay:
≥98% (HPLC)
Form:
powder
Storage condition:
desiccated

CHF 138.00


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Nome del prodotto

iCRT3,

assay

≥98% (HPLC)

Quality Segment

form

powder

storage condition

desiccated

color

white to tan

solubility

DMSO: ≥5 mg/mL

storage temp.

2-8°C

SMILES string

CCc1ccc(cc1)-c2nc(CSCC(=O)NCCc3ccccc3)c(C)o2

InChI

1S/C23H26N2O2S/c1-3-18-9-11-20(12-10-18)23-25-21(17(2)27-23)15-28-16-22(26)24-14-13-19-7-5-4-6-8-19/h4-12H,3,13-16H2,1-2H3,(H,24,26)

InChI key

QTDYVSIBWGVBKU-UHFFFAOYSA-N

General description

iCRT3 is a small cell-permeable oxazole compound. It blocks cytokine secretion in lipopolysaccharide (LPS)-stimulated macrophages.

Application

iCRT3 has been used to inhibit the interactions between β-catenin and transcription factor (TCF).
iCRT3 has been used:
  • for β- catenin inhibition in dual luciferase assay
  • to inhibit β-catenin /TCF interactions and their transcriptional activity
  • as wingless/tailess (wnt) antagonist, to determine Wnt/β-catenin signaling is essential for PROX1-mediated regulation of forkhead box protein C2 (FOXC2)(3)catenin inhibition in dual luciferase assay
  • to inhibit β- catenin /TCF interactions and their transcriptional activity
  • as wingless/tailess (wnt) antagonist, to determine Wnt/β-catenin signaling is essential for PROX1-mediated regulation of forkhead box protein C2 (FOXC2)

Biochem/physiol Actions

The key mediator of Wnt signaling is the transcriptional co-activator b-catenin. In the cytoplasm, b-catenin is tightly bound to a complex that includes Axin and GSK-3b. Stimulation causes b-catenin stabilization, translocation to the nucleus and association with TCF4 to initiate transcription of responsive genes, referred to as Catenin Responsive Transcription (CRT). Virtually all Wnt-associated cancers are the result of misregulated CRT. Three inhibitors of CRT (iCRT) were identified in a screen that employed RNAi based knockdown of Axin, which stimulates CRT without affecting upstream mechanisms such as GSK activity, transduction by disheveled / frizzled, etc. These compounds are potent inhibitors of CRT reporter genes, as well as endogenous gene targets. The compounds also disrupt b-catenin-TCF4 interaction in a dose dependent manner, and cause G0/G1 arrest in colon tumor lines.
Wnt / b-catenin pathway inhibitor

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219332
iCRT3

Sigma-Aldrich

SML0211

iCRT3

description

-

description

The β-Catenin/Tcf Inhibitor III, iCRT3 controls the biological activity of β-Catenin/Tcf. This small molecule/inhibitor is primarily used for Biochemicals applications.

assay

≥98% (HPLC)

assay

≥95% (HPLC)

form

powder

form

powder

Quality Level

100

Quality Level

100

storage temp.

2-8°C

storage temp.

−20°C

solubility

DMSO: ≥5 mg/mL

solubility

DMSO: 50 mg/mL

storage condition

desiccated

storage condition

protect from light, OK to freeze


Classe di stoccaggio

11 - Combustible Solids

Che succede?

WGK 3



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