ID: ALA3318896

Max Phase: Preclinical

Molecular Formula: C8H15NO

Molecular Weight: 141.21

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O[C@H]1CC[C@H]2CCN[C@H]2C1

Standard InChI:  InChI=1S/C8H15NO/c10-7-2-1-6-3-4-9-8(6)5-7/h6-10H,1-5H2/t6-,7-,8-/m0/s1

Standard InChI Key:  WPMCENBDLQRRNM-FXQIFTODSA-N

Associated Targets(non-human)

Neuronal acetylcholine receptor; alpha3/beta4 1368 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Nicotinic acetylcholine receptor alpha-4/beta-2 112 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; 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: 141.21Molecular Weight (Monoisotopic): 141.1154AlogP: 0.51#Rotatable Bonds: 0
Polar Surface Area: 32.26Molecular Species: BASEHBA: 2HBD: 2
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 11.08CX LogP: 0.04CX LogD: -3.07
Aromatic Rings: 0Heavy Atoms: 10QED Weighted: 0.51Np Likeness Score: 2.13

References

1. Jepsen TH, Jensen AA, Lund MH, Glibstrup E, Kristensen JL..  (2014)  Synthesis and Pharmacological Evaluation of DHβE Analogues as Neuronal Nicotinic Acetylcholine Receptor Antagonists.,  (7): [PMID:25050162] [10.1021/ml500094c]

Source