ID: ALA395304

Max Phase: Preclinical

Molecular Formula: C22H28N2O

Molecular Weight: 336.48

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O[C@@H]1CCC2CN(CCc3ccccc3)C1CN2Cc1ccccc1

Standard InChI:  InChI=1S/C22H28N2O/c25-22-12-11-20-16-23(14-13-18-7-3-1-4-8-18)21(22)17-24(20)15-19-9-5-2-6-10-19/h1-10,20-22,25H,11-17H2/t20?,21?,22-/m1/s1

Standard InChI Key:  KNLILHFSKCATHQ-LZBANZJXSA-N

Associated Targets(non-human)

Sigma-1 receptor 3326 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Kappa opioid receptor 4577 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: 336.48Molecular Weight (Monoisotopic): 336.2202AlogP: 2.94#Rotatable Bonds: 5
Polar Surface Area: 26.71Molecular Species: BASEHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.51CX LogP: 3.67CX LogD: 2.53
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.91Np Likeness Score: -0.11

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