ID: ALA3127010

Max Phase: Preclinical

Molecular Formula: C27H27NO5

Molecular Weight: 445.52

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCN(CCCOc1ccc(-c2coc3cc(O)cc(O)c3c2=O)cc1)Cc1ccccc1

Standard InChI:  InChI=1S/C27H27NO5/c1-2-28(17-19-7-4-3-5-8-19)13-6-14-32-22-11-9-20(10-12-22)23-18-33-25-16-21(29)15-24(30)26(25)27(23)31/h3-5,7-12,15-16,18,29-30H,2,6,13-14,17H2,1H3

Standard InChI Key:  AQMLTOWGCRQUOF-UHFFFAOYSA-N

Associated Targets(Human)

Acetylcholinesterase 18204 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Butyrylcholinesterase 745 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Acetylcholinesterase 12221 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Acetylcholinesterase 2577 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

Properties

Molecular Weight: 445.52Molecular Weight (Monoisotopic): 445.1889AlogP: 5.16#Rotatable Bonds: 9
Polar Surface Area: 83.14Molecular Species: BASEHBA: 6HBD: 2
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 6.55CX Basic pKa: 9.27CX LogP: 3.91CX LogD: 3.94
Aromatic Rings: 4Heavy Atoms: 33QED Weighted: 0.35Np Likeness Score: 0.02

References

1. Qiang X, Sang Z, Yuan W, Li Y, Liu Q, Bai P, Shi Y, Ang W, Tan Z, Deng Y..  (2014)  Design, synthesis and evaluation of genistein-O-alkylbenzylamines as potential multifunctional agents for the treatment of Alzheimer's disease.,  76  [PMID:24589487] [10.1016/j.ejmech.2014.02.045]

Source