(E)-1-(4-Amino-2-hydroxyphenyl)-3-(3,5-bis-(trifluoromethyl)phenyl)prop-2-en-1-one

ID: ALA2419935

Chembl Id: CHEMBL2419935

PubChem CID: 71819502

Max Phase: Preclinical

Molecular Formula: C17H11F6NO2

Molecular Weight: 375.27

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Nc1ccc(C(=O)/C=C/c2cc(C(F)(F)F)cc(C(F)(F)F)c2)c(O)c1

Standard InChI:  InChI=1S/C17H11F6NO2/c18-16(19,20)10-5-9(6-11(7-10)17(21,22)23)1-4-14(25)13-3-2-12(24)8-15(13)26/h1-8,26H,24H2/b4-1+

Standard InChI Key:  ZAKATBBJLDVIBJ-DAFODLJHSA-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: 375.27Molecular Weight (Monoisotopic): 375.0694AlogP: 4.91#Rotatable Bonds: 3
Polar Surface Area: 63.32Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: HBA (Lipinski): 3HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: 7.40CX Basic pKa: 2.76CX LogP: 5.16CX LogD: 4.86
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.35Np Likeness Score: -0.17

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