|   PNU 74654 structure | Common Name | PNU 74654 | ||
|---|---|---|---|---|
| CAS Number | 113906-27-7 | Molecular Weight | 320.342 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | N/A | |
| Molecular Formula | C19H16N2O3 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | N/A | |
| Symbol |   GHS07 | Signal Word | Warning | |
| Use of PNU 74654PNU-74654 is an inhibitor of Wnt/β-catenin pathway with an IC50 of 129.8 μM in NCI-H295 cell. | 
| Name | PNU 74654,2-Phenoxybenzoicacid-[(5-methyl-2-furanyl)methylene]hydrazide | 
|---|---|
| Synonym | More Synonyms | 
| Description | PNU-74654 is an inhibitor of Wnt/β-catenin pathway with an IC50 of 129.8 μM in NCI-H295 cell. | 
|---|---|
| Related Catalog | |
| Target | 129.8 μM (Wnt/β-catenin, NCI-H295 cell)[1] | 
| In Vitro | PNU-74654 binds to β-catenin with a KD of 450 nM. The Tcf3/Tcf4-binding surface on β-catenin contains a well-defined hot spot around residues K435 and R469. The binding mode of PNU-74654 involves the two narrow pockets on either side of this hot spot[2]. In NCI-H295 cells,PNU-74654 significantly decreases cell proliferation 96 h after treatment, increases early and late apoptosis, decreases nuclear beta-catenin accumulation, impairs CTNNB1/beta-catenin expression and increases beta-catenin target genes 48 h after treatment. No effects are observed on HeLa cells. In NCI-H295 cells, PNU-74654 decreases cortisol, testosterone and androstenedione secretion 24 and 48 h after treatment. The SF1 and CYP21A2 mRNA expression as well as the protein levels of STAR and aldosterone synthase are decreased in NCI-H295 cells after 48 h PNU-74654 treatment. In Y1 cells, PNU-74654 impairs corticosterone secretion 24 h after treatment but does not decrease cell viability[1]. | 
| Cell Assay | The PNU-74654 compound is dissolved in DMSO at stock concentrations of 31.2 mM. For working solutions, PNU-74654 is diluted 100X in growth medium with no serum deprivation. NCI-H295 cells are plated at 200,000 cells per well in 24-well plates for gene expression, protein analysis and adrenal steroid measurements. After 48 h, cells are treated with vehicle (0.1%-0.4% DMSO) or 10, 50, 100 and 200 μM PNU-74654. After 24 and 48 h, medium supernatants are collected for adrenal steroid measurements[1]. | 
| References | 
| Density | 1.2±0.1 g/cm3 | 
|---|---|
| Molecular Formula | C19H16N2O3 | 
| Molecular Weight | 320.342 | 
| Exact Mass | 320.116089 | 
| PSA | 63.83000 | 
| LogP | 3.90 | 
| Index of Refraction | 1.593 | 
| Storage condition | -20℃ | 
| An increase in glucosylceramide synthase induces Bcl-xL-mediated cell survival in vinorelbine-resistant lung adenocarcinoma cells. Oncotarget 6 , 20513-24, (2015) Reversing drug resistance with concurrent treatment confers anticancer benefits. In this study, we investigated the potential mechanism of glucosylceramide synthase (GCS)-mediated vinca alkaloid vinor... | |
| The WTX Tumor Suppressor Interacts with the Transcriptional Corepressor TRIM28. J. Biol. Chem. 290 , 14381-90, (2015) WTX encodes a tumor suppressor implicated in the pediatric kidney cancer Wilms tumor and in mesenchymal differentiation with potentially distinct functions in the cytoplasm, at the plasma membrane, an... | |
| Inhibition of the Tcf/beta-catenin complex increases apoptosis and impairs adrenocortical tumor cell proliferation and adrenal steroidogenesis. .PubMed ID To date, there is no effective therapy for patients with advanced/metastatic adrenocortical cancer (ACC). The activation of the Wnt/beta-catenin signaling is frequent in ACC and this pathway is a prom... | 
| Benzoic acid, 2-phenoxy-, 2-[(1E)-(5-methyl-2-furanyl)methylene]hydrazide | 
| N'-[(E)-(5-Methyl-2-furyl)methylene]-2-phenoxybenzohydrazide | 
| N'-[(E)-(5-methylfuran-2-yl)methylidene]-2-phenoxybenzohydrazide | 
| PNU-74654 |