PNU 74654 - 10mM in DMSO , CAS No.113906-27-7

CAS: 113906-27-7 Cat. No.: P420694 Summenformel: C₁₉H₁₆N₂O₃ Molekulargewicht: 320.34 EG-Nummer: 631-232-6 PubChem CID: 9836739

GRADE & PURITY 10mM in DMSO

Synonyms

HMS3413P04 | HY-101130 | PNU74654 | PNU-74654 | J-003040 | NSC755984 | NSC-755984 | CCG-208115 | N-[(E)-(5-Methylfuran-2-yl)methylideneamino]-2-phenoxybenzamide | SCHEMBL3514174 | BDBM50436058 | AC-33054 | PNU 74654 | 2-Phenoxybenzoic acid-[(5-methyl-2-fu

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Übersicht

application：

PNU-74654 has been used:

as a β-catenin signaling inhibitor to study its effects on the funnel cartilage differentiation in Sepia sp. embryos

as a Wnt signaling inhibitor to study its effects on glycogen synthase kinase 3β (GSK-3β) inhibition in prostate cancer cell lines

as a Wnt signaling inhibitor to study its effects on leptin-induced cell proliferation in breast cancer cells

Specifications

Synonyme

HMS3413P04 | HY-101130 | PNU74654 | PNU-74654 | J-003040 | NSC755984 | NSC-755984 | CCG-208115 | N-[(E)-(5-Methylfuran-2-yl)methylideneamino]-2-phenoxybenzamide | SCHEMBL3514174 | BDBM50436058 | AC-33054 | PNU 74654 | 2-Phenoxybenzoic acid-[(5-methyl-2-fu

Spezifikationen & Reinheit

10mM in DMSO

Biochemische und physiologische Mechanismen

Wnt signaling pathway blocker. Inhibits Wnt/β-catenin pathway. Blocks the protein-protein interaction between β-catenin and TCF. Antitumor effects.PNU-74654 inhibits the Wnt-β catenin pathway by blocking the interaction between β-catenin and TCF (T cell f

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Aktionsart

INHIBITOR

Namen und Kennungen

• Pubchem Sid: 528766676
• Kanonisches Lächeln: CC1=CC=C(O1)C=NNC(=O)C2=CC=CC=C2OC3=CC=CC=C3
• IUPAC Name: N-[(E)-(5-methylfuran-2-yl)methylideneamino]-2-phenoxybenzamide
• InChIKey: JJEDWBQZCRESJL-DEDYPNTBSA-N
• INCHI: 1S/C19H16N2O3/c1-14-11-12-16(23-14)13-20-21-19(22)17-9-5-6-10-18(17)24-15-7-3-2-4-8-15/h2-13H,1H3,(H,21,22)/b20-13+
• Isomere SMILES: CC1=CC=C(O1)/C=N/NC(=O)C2=CC=CC=C2OC3=CC=CC=C3
• PubChem CID: 9836739
• Molekulargewicht: 320.34

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Klasse Benzene and substituted derivatives
      • Subclass Diphenylethers

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Benzene and substituted derivatives
• Subclass: Diphenylethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Diphenylethers
• Alternative Parents: Diarylethers Benzoic acids and derivatives Phenoxy compounds Phenol ethers Benzoyl derivatives Heteroaromatic compounds Furans Oxacyclic compounds Carboxylic acids and derivatives Organonitrogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Diphenylether - Diaryl ether - Benzoic acid or derivatives - Benzoyl - Phenoxy compound - Phenol ether - Heteroaromatic compound - Furan - Oxacycle - Organoheterocyclic compound - Ether - Carboxylic acid derivative - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Aromatic heteromonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as diphenylethers. These are aromatic compounds containing two benzene rings linked to each other through an ether group.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Zugehörige Ziele (menschlich)

CTNNB1 Tchem Catenin beta-1 (1 Activities)

Discover Target: CTNNB1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CTNNB1 Tchem Catenin beta-1 (517 Activities)

Discover Target: CTNNB1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CTNNB1 Tchem TCF4/beta-catenin (616 Activities)

Discover Target: CTNNB1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CTNNB1 Tchem TCF4-CTNNB1 complex (25 Activities)

Discover Target: CTNNB1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Zugehörige Ziele (nicht menschlich)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Molekulargewicht: 320.300 g/mol
• XLogP3: 4.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 320.116 Da
• Monoisotopic Mass: 320.116 Da
• Topological Polar Surface Area: 63.800 Ų
• Heavy Atom Count: 24
• Formal Charge: 0
• Complexity: 434.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 1
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1

Referenzen

1. Fang Lini, Tao Yang, Che Guoying, Yun Yongzi, Ren Min, Liu Yujie.  (2024)  WSB1, as an E3 ligase, restrains myocardial ischemia–reperfusion injury by activating β-catenin signaling via promoting GSK3β ubiquitination.  MOLECULAR MEDICINE,  30  (1): (1-16).  [PMID:38395742] [10.1186/s10020-024-00800-3]