(2E,2'E)-1,1'-(1,3-phenylene)bis(3-(2-methoxyphenyl)prop-2-en-1-one)

ID: ALA4246378

Chembl Id: CHEMBL4246378

PubChem CID: 145984545

Max Phase: Preclinical

Molecular Formula: C26H22O4

Molecular Weight: 398.46

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1ccccc1/C=C/C(=O)c1cccc(C(=O)/C=C/c2ccccc2OC)c1

Standard InChI:  InChI=1S/C26H22O4/c1-29-25-12-5-3-8-19(25)14-16-23(27)21-10-7-11-22(18-21)24(28)17-15-20-9-4-6-13-26(20)30-2/h3-18H,1-2H3/b16-14+,17-15+

Standard InChI Key:  QDCJAQDMQKEGPR-YXLFCKQPSA-N

Alternative Forms

  1. Parent:

    ALA4246378

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Associated Targets(Human)

A-431 (6446 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DLD-1 (17511 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
WRL68 (207 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ehrlich (1318 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 398.46Molecular Weight (Monoisotopic): 398.1518AlogP: 5.50#Rotatable Bonds: 8
Polar Surface Area: 52.60Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 5.49CX LogD: 5.49
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.37Np Likeness Score: -0.20

References

1. Khwaja S, Fatima K, Hasanain M, Behera C, Kour A, Singh A, Luqman S, Sarkar J, Chanda D, Shanker K, Gupta AK, Mondhe DM, Negi AS..  (2018)  Antiproliferative efficacy of curcumin mimics through microtubule destabilization.,  151  [PMID:29605808] [10.1016/j.ejmech.2018.03.063]

Source