ID: ALA2177698

Max Phase: Preclinical

Molecular Formula: C17H25ClN2O4

Molecular Weight: 320.39

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCN(C)C(=O)Oc1cccc2c1C(CCC(=O)OC)CN2C.Cl

Standard InChI:  InChI=1S/C17H24N2O4.ClH/c1-5-18(2)17(21)23-14-8-6-7-13-16(14)12(11-19(13)3)9-10-15(20)22-4;/h6-8,12H,5,9-11H2,1-4H3;1H

Standard InChI Key:  LMUIGNVZNKCFIM-UHFFFAOYSA-N

Associated Targets(non-human)

H9c2 3506 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Butyrylcholinesterase 805 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Acetylcholinesterase 1035 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: 320.39Molecular Weight (Monoisotopic): 320.1736AlogP: 2.62#Rotatable Bonds: 5
Polar Surface Area: 59.08Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 2.48CX LogP: 2.28CX LogD: 2.28
Aromatic Rings: 1Heavy Atoms: 23QED Weighted: 0.78Np Likeness Score: -0.37

References

1. Yanovsky I, Finkin-Groner E, Zaikin A, Lerman L, Shalom H, Zeeli S, Weill T, Ginsburg I, Nudelman A, Weinstock M..  (2012)  Carbamate derivatives of indolines as cholinesterase inhibitors and antioxidants for the treatment of Alzheimer's disease.,  55  (23): [PMID:23151013] [10.1021/jm301411g]

Source