ID: ALA2281489

Max Phase: Preclinical

Molecular Formula: C19H16O4

Molecular Weight: 308.33

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(/C=C/c2cc(=O)c3ccccc3o2)cc1OC

Standard InChI:  InChI=1S/C19H16O4/c1-21-18-10-8-13(11-19(18)22-2)7-9-14-12-16(20)15-5-3-4-6-17(15)23-14/h3-12H,1-2H3/b9-7+

Standard InChI Key:  DLGKFWXMKAOKRL-VQHVLOKHSA-N

Associated Targets(Human)

OVCAR 348 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HeLa 62764 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

AGS 1999 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

Properties

Molecular Weight: 308.33Molecular Weight (Monoisotopic): 308.1049AlogP: 3.98#Rotatable Bonds: 4
Polar Surface Area: 48.67Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.53CX LogD: 3.53
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.73Np Likeness Score: 0.32

References

1. Lin C, Lu P, Yang C, Hulme C, Shaw AY.  (2013)  Structureactivity relationship study of growth inhibitory 2-styrylchromones against carcinoma cells,  22  (5): [10.1007/s00044-012-0232-6]

Source