ID: ALA3321877

Max Phase: Preclinical

Molecular Formula: C16H24N2O3

Molecular Weight: 292.38

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(CN2CCCCC2)cc1OC(=O)N(C)C

Standard InChI:  InChI=1S/C16H24N2O3/c1-17(2)16(19)21-15-11-13(7-8-14(15)20-3)12-18-9-5-4-6-10-18/h7-8,11H,4-6,9-10,12H2,1-3H3

Standard InChI Key:  CIHXFRDDFGQHHD-UHFFFAOYSA-N

Associated Targets(Human)

Amyloid-beta A4 protein 8510 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Acetylcholinesterase 2577 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Butyrylcholinesterase 745 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: 292.38Molecular Weight (Monoisotopic): 292.1787AlogP: 2.74#Rotatable Bonds: 4
Polar Surface Area: 42.01Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.25CX LogP: 2.33CX LogD: 1.43
Aromatic Rings: 1Heavy Atoms: 21QED Weighted: 0.86Np Likeness Score: -1.00

References

1. Li Y, Peng P, Tang L, Hu Y, Hu Y, Sheng R..  (2014)  Design, synthesis and evaluation of rivastigmine and curcumin hybrids as site-activated multitarget-directed ligands for Alzheimer's disease therapy.,  22  (17): [PMID:25082512] [10.1016/j.bmc.2014.07.009]

Source