ID: ALA3318889

Max Phase: Preclinical

Molecular Formula: C10H19NO

Molecular Weight: 169.27

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CO[C@H]1CC[C@H]2CCN(C)[C@H]2C1

Standard InChI:  InChI=1S/C10H19NO/c1-11-6-5-8-3-4-9(12-2)7-10(8)11/h8-10H,3-7H2,1-2H3/t8-,9-,10-/m0/s1

Standard InChI Key:  PNDUXUALYZWZES-GUBZILKMSA-N

Associated Targets(non-human)

Neuronal acetylcholine receptor; alpha4/beta2 3557 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

Nicotinic acetylcholine receptor alpha-4/beta-2 112 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: 169.27Molecular Weight (Monoisotopic): 169.1467AlogP: 1.51#Rotatable Bonds: 1
Polar Surface Area: 12.47Molecular Species: BASEHBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 10.27CX LogP: 1.06CX LogD: -1.71
Aromatic Rings: 0Heavy Atoms: 12QED Weighted: 0.59Np Likeness Score: 1.02

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