3-(4-methoxyphenyl)-7-(2-((1,2,3,4-tetrahydroacridin-9-yl)amino)ethoxy)-4H-chromen-4-one

ID: ALA4438929

Chembl Id: CHEMBL4438929

PubChem CID: 155513598

Max Phase: Preclinical

Molecular Formula: C31H28N2O4

Molecular Weight: 492.58

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1ccc(-c2coc3cc(OCCNc4c5c(nc6ccccc46)CCCC5)ccc3c2=O)cc1

Standard InChI:  InChI=1S/C31H28N2O4/c1-35-21-12-10-20(11-13-21)26-19-37-29-18-22(14-15-25(29)31(26)34)36-17-16-32-30-23-6-2-4-8-27(23)33-28-9-5-3-7-24(28)30/h2,4,6,8,10-15,18-19H,3,5,7,9,16-17H2,1H3,(H,32,33)

Standard InChI Key:  YLNDHUJSURMTDP-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4438929

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Associated Targets(Human)

HRH3 Tclin Histamine H3 receptor (10389 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Ache Acetylcholinesterase (1323 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bche Butyrylcholinesterase (210 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 492.58Molecular Weight (Monoisotopic): 492.2049AlogP: 6.39#Rotatable Bonds: 7
Polar Surface Area: 73.59Molecular Species: BASEHBA: 6HBD: 1
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 8.88CX LogP: 5.78CX LogD: 4.45
Aromatic Rings: 5Heavy Atoms: 37QED Weighted: 0.27Np Likeness Score: -0.40

References

1. Wang D, Hu M, Li X, Zhang D, Chen C, Fu J, Shao S, Shi G, Zhou Y, Wu S, Zhang T..  (2019)  Design, synthesis, and evaluation of isoflavone analogs as multifunctional agents for the treatment of Alzheimer's disease.,  168  [PMID:30822710] [10.1016/j.ejmech.2019.02.053]

Source