7-Hydroxy-2-(5-(4-methoxyphenyl)thiophen-2-yl)-4H-chromen-4-one

ID: ALA2419924

Chembl Id: CHEMBL2419924

PubChem CID: 71819495

Max Phase: Preclinical

Molecular Formula: C20H14O4S

Molecular Weight: 350.40

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1ccc(-c2ccc(-c3cc(=O)c4ccc(O)cc4o3)s2)cc1

Standard InChI:  InChI=1S/C20H14O4S/c1-23-14-5-2-12(3-6-14)19-8-9-20(25-19)18-11-16(22)15-7-4-13(21)10-17(15)24-18/h2-11,21H,1H3

Standard InChI Key:  OXOWGPLWTXGEHY-UHFFFAOYSA-N

Associated Targets(non-human)

Nr1h2 Oxysterols receptor LXR-beta (116 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 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: 350.40Molecular Weight (Monoisotopic): 350.0613AlogP: 4.90#Rotatable Bonds: 3
Polar Surface Area: 59.67Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 6.50CX Basic pKa: CX LogP: 4.06CX LogD: 3.14
Aromatic Rings: 4Heavy Atoms: 25QED Weighted: 0.57Np Likeness Score: 0.24

References

1. Hu Y, Yang Y, Yu Y, Wen G, Shang N, Zhuang W, Lu D, Zhou B, Liang B, Yue X, Li F, Du J, Bu X..  (2013)  Synthesis and identification of new flavonoids targeting liver X receptor β involved pathway as potential facilitators of Aβ clearance with reduced lipid accumulation.,  56  (15): [PMID:23844653] [10.1021/jm301913k]
2. Chen M, Yang F, Kang J, Gan H, Lai X, Gao Y..  (2018)  Discovery of molecular mechanism of a clinical herbal formula upregulating serum HDL-c levels in treatment of metabolic syndrome by in vivo and computational studies.,  28  (2): [PMID:29196136] [10.1016/j.bmcl.2017.11.033]

Source