3-(4-methoxyphenyl)-N-methyl-N-pentyl-4-phenyl-but-3-enamide

ID: ALA4635948

Chembl Id: CHEMBL4635948

PubChem CID: 156014670

Max Phase: Preclinical

Molecular Formula: C23H29NO2

Molecular Weight: 351.49

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCCCN(C)C(=O)C/C(=C\c1ccccc1)c1ccc(OC)cc1

Standard InChI:  InChI=1S/C23H29NO2/c1-4-5-9-16-24(2)23(25)18-21(17-19-10-7-6-8-11-19)20-12-14-22(26-3)15-13-20/h6-8,10-15,17H,4-5,9,16,18H2,1-3H3/b21-17+

Standard InChI Key:  LAZHTIMUMJKNDH-HEHNFIMWSA-N

Alternative Forms

  1. Parent:

    ALA4635948

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Associated Targets(Human)

MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Esr2 Estrogen receptor beta (51 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 351.49Molecular Weight (Monoisotopic): 351.2198AlogP: 5.27#Rotatable Bonds: 9
Polar Surface Area: 29.54Molecular Species: NEUTRALHBA: 2HBD:
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): #RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 4.99CX LogD: 4.99
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.45Np Likeness Score: -0.50

References

1. Imran Ahamad M, Prakash R, John AA, Wani Z, Yadav D, Bawankule DU, Luqman S, Khan F, Singh D, Gupta A..  (2020)  Induced osteoblast differentiation by amide derivatives of stilbene: The possible osteogenic agents.,  30  (11): [PMID:32247734] [10.1016/j.bmcl.2020.127138]

Source