ID: ALA390022

Max Phase: Preclinical

Molecular Formula: C15H22N2O

Molecular Weight: 246.35

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CN1CC2CC[C@H](O)C1CN2Cc1ccccc1

Standard InChI:  InChI=1S/C15H22N2O/c1-16-10-13-7-8-15(18)14(16)11-17(13)9-12-5-3-2-4-6-12/h2-6,13-15,18H,7-11H2,1H3/t13?,14?,15-/m0/s1

Standard InChI Key:  NHNVWOOBLVBHIJ-NRXISQOPSA-N

Associated Targets(non-human)

Kappa opioid receptor 4577 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Sigma-1 receptor 3326 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mu opioid receptor 3620 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: 246.35Molecular Weight (Monoisotopic): 246.1732AlogP: 1.33#Rotatable Bonds: 2
Polar Surface Area: 26.71Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.39CX LogP: 1.66CX LogD: 0.63
Aromatic Rings: 1Heavy Atoms: 18QED Weighted: 0.85Np Likeness Score: 0.22

References

1. Weigl M, Wünsch B..  (2007)  Synthesis of bridged piperazines with sigma receptor affinity.,  42  (10): [PMID:17420073] [10.1016/j.ejmech.2007.02.005]

Source