ID: ALA1204343

Max Phase: Preclinical

Molecular Formula: C23H31Cl2FN2O

Molecular Weight: 368.50

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cl.Cl.O[C@@H]1CCN(Cc2ccc(F)cc2)C[C@H]1N1CCC(c2ccccc2)CC1

Standard InChI:  InChI=1S/C23H29FN2O.2ClH/c24-21-8-6-18(7-9-21)16-25-13-12-23(27)22(17-25)26-14-10-20(11-15-26)19-4-2-1-3-5-19;;/h1-9,20,22-23,27H,10-17H2;2*1H/t22-,23-;;/m1../s1

Standard InChI Key:  FOPXXIUICYTUFQ-TVLOEWINSA-N

Associated Targets(non-human)

Vesicular acetylcholine transporter 105 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: 368.50Molecular Weight (Monoisotopic): 368.2264AlogP: 3.64#Rotatable Bonds: 4
Polar Surface Area: 26.71Molecular Species: BASEHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.99CX LogP: 3.67CX LogD: 2.07
Aromatic Rings: 2Heavy Atoms: 27QED Weighted: 0.89Np Likeness Score: -0.70

References

1. Efange SM, Khare A, Parsons SM, Bau R, Metzenthin T..  (1993)  Nonsymmetrical bipiperidyls as inhibitors of vesicular acetylcholine storage.,  36  (8): [PMID:8478910] [10.1021/jm00060a005]

Source