(E)-1-(4-(Dimethylamino)-2-hydroxyphenyl)-3-(5-methylfuran-2-yl)prop-2-en-1-one

ID: ALA2419916

Chembl Id: CHEMBL2419916

PubChem CID: 71817629

Max Phase: Preclinical

Molecular Formula: C16H17NO3

Molecular Weight: 271.32

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1ccc(/C=C/C(=O)c2ccc(N(C)C)cc2O)o1

Standard InChI:  InChI=1S/C16H17NO3/c1-11-4-6-13(20-11)7-9-15(18)14-8-5-12(17(2)3)10-16(14)19/h4-10,19H,1-3H3/b9-7+

Standard InChI Key:  CXFADWSMBPRWFM-VQHVLOKHSA-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: 271.32Molecular Weight (Monoisotopic): 271.1208AlogP: 3.26#Rotatable Bonds: 4
Polar Surface Area: 53.68Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 7.36CX Basic pKa: 2.59CX LogP: 3.60CX LogD: 3.28
Aromatic Rings: 2Heavy Atoms: 20QED Weighted: 0.68Np Likeness Score: -0.61

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