ID: ALA2312561

Max Phase: Preclinical

Molecular Formula: C11H18N2O

Molecular Weight: 194.28

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C[C@H](CCOc1cccnc1)N(C)C

Standard InChI:  InChI=1S/C11H18N2O/c1-10(13(2)3)6-8-14-11-5-4-7-12-9-11/h4-5,7,9-10H,6,8H2,1-3H3/t10-/m1/s1

Standard InChI Key:  CJOVRHGBQYDTNU-SNVBAGLBSA-N

Associated Targets(non-human)

Acetylcholine-binding protein 240 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Neuronal acetylcholine receptor protein alpha-7 subunit 3047 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Neuronal acetylcholine receptor; alpha4/beta4 595 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Neuronal acetylcholine receptor; alpha3/beta4 1368 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Neuronal acetylcholine receptor; alpha4/beta2 3557 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: 194.28Molecular Weight (Monoisotopic): 194.1419AlogP: 1.80#Rotatable Bonds: 5
Polar Surface Area: 25.36Molecular Species: BASEHBA: 3HBD: 0
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 9.54CX LogP: 1.09CX LogD: -1.03
Aromatic Rings: 1Heavy Atoms: 14QED Weighted: 0.71Np Likeness Score: -1.23

References

1. Ussing CA, Hansen CP, Petersen JG, Jensen AA, Rohde LA, Ahring PK, Nielsen EØ, Kastrup JS, Gajhede M, Frølund B, Balle T..  (2013)  Synthesis, pharmacology, and biostructural characterization of novel α4β2 nicotinic acetylcholine receptor agonists.,  56  (3): [PMID:23256554] [10.1021/jm301409f]

Source