3-(4-Hydroxy-phenyl)-2-phenyl-3-p-tolyl-acrylonitrile

ID: ALA291639

Chembl Id: CHEMBL291639

PubChem CID: 14537259

Max Phase: Preclinical

Molecular Formula: C22H17NO

Molecular Weight: 311.38

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1ccc(/C(=C(\C#N)c2ccccc2)c2ccc(O)cc2)cc1

Standard InChI:  InChI=1S/C22H17NO/c1-16-7-9-18(10-8-16)22(19-11-13-20(24)14-12-19)21(15-23)17-5-3-2-4-6-17/h2-14,24H,1H3/b22-21-

Standard InChI Key:  YCHUKCZZGUEKDH-DQRAZIAOSA-N

Associated Targets(Human)

MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BT-20 (503 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7S (266 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

ESR2 Estrogen receptor (627 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Prkca Protein kinase C, PKC; classical (135 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: 311.38Molecular Weight (Monoisotopic): 311.1310AlogP: 5.18#Rotatable Bonds: 3
Polar Surface Area: 44.02Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 1HBA (Lipinski): 2HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 7.89CX Basic pKa: CX LogP: 5.67CX LogD: 5.55
Aromatic Rings: 3Heavy Atoms: 24QED Weighted: 0.53Np Likeness Score: -0.05

References

1. Bignon E, Pons M, Crastes de Paulet AC, Doré JC, Gilbert J, Abecassis J, Miquel JF, Ojasoo T, Raynaud JP..  (1989)  Effect of triphenylacrylonitrile derivatives on estradiol-receptor binding and on human breast cancer cell growth.,  32  (9): [PMID:2769681] [10.1021/jm00129a013]
2. Doré JC, Gilbert J, Bignon E, Crastes de Paulet A, Ojasoo T, Pons M, Raynaud JP, Miquel JF..  (1992)  Multivariate analysis by the minimum spanning tree method of the structural determinants of diphenylethylenes and triphenylacrylonitriles implicated in estrogen receptor binding, protein kinase C activity, and MCF7 cell proliferation.,  35  (3): [PMID:1738150] [10.1021/jm00081a021]

Source