ID: ALA3318894

Max Phase: Preclinical

Molecular Formula: C16H23NO

Molecular Weight: 245.37

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CN1CC[C@@H]2CC[C@H](OCc3ccccc3)C[C@@H]21

Standard InChI:  InChI=1S/C16H23NO/c1-17-10-9-14-7-8-15(11-16(14)17)18-12-13-5-3-2-4-6-13/h2-6,14-16H,7-12H2,1H3/t14-,15-,16-/m0/s1

Standard InChI Key:  XJBIRLCXDMVDOD-JYJNAYRXSA-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: 245.37Molecular Weight (Monoisotopic): 245.1780AlogP: 3.08#Rotatable Bonds: 3
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: 10.14CX LogP: 2.79CX LogD: 0.12
Aromatic Rings: 1Heavy Atoms: 18QED Weighted: 0.81Np Likeness Score: 0.44

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