(E)-1-(4-Chlorophenyl)-3-(3-ethoxy-4-hydroxyphenyl)prop-2-en-1-one

ID: ALA4160709

Chembl Id: CHEMBL4160709

PubChem CID: 8829225

Max Phase: Preclinical

Molecular Formula: C17H15ClO3

Molecular Weight: 302.76

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCOc1cc(/C=C/C(=O)c2ccc(Cl)cc2)ccc1O

Standard InChI:  InChI=1S/C17H15ClO3/c1-2-21-17-11-12(4-10-16(17)20)3-9-15(19)13-5-7-14(18)8-6-13/h3-11,20H,2H2,1H3/b9-3+

Standard InChI Key:  HOKXZSSLXZDGLC-YCRREMRBSA-N

Associated Targets(Human)

CXCL12 Tchem Stromal cell-derived factor 1 (156 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: 302.76Molecular Weight (Monoisotopic): 302.0710AlogP: 4.34#Rotatable Bonds: 5
Polar Surface Area: 46.53Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 9.49CX Basic pKa: CX LogP: 4.39CX LogD: 4.39
Aromatic Rings: 2Heavy Atoms: 21QED Weighted: 0.66Np Likeness Score: -0.18

References

1. Regenass P, Abboud D, Daubeuf F, Lehalle C, Gizzi P, Riché S, Hachet-Haas M, Rohmer F, Gasparik V, Boeglin D, Haiech J, Knehans T, Rognan D, Heissler D, Marsol C, Villa P, Galzi JL, Hibert M, Frossard N, Bonnet D..  (2018)  Discovery of a Locally and Orally Active CXCL12 Neutraligand (LIT-927) with Anti-inflammatory Effect in a Murine Model of Allergic Airway Hypereosinophilia.,  61  (17): [PMID:30106292] [10.1021/acs.jmedchem.8b00657]

Source