| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA244652
Max Phase: Preclinical
Molecular Formula: C23H30N2O
Molecular Weight: 350.51
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: COC1CCC2CN(CCc3ccccc3)C1CN2Cc1ccccc1
Standard InChI: InChI=1S/C23H30N2O/c1-26-23-13-12-21-17-24(15-14-19-8-4-2-5-9-19)22(23)18-25(21)16-20-10-6-3-7-11-20/h2-11,21-23H,12-18H2,1H3
Standard InChI Key: WYUPWHUGPAKEOJ-UHFFFAOYSA-N
Associated Targets(non-human)
Sigma-1 receptor 3326 Activities
Kappa opioid receptor 4577 Activities
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Mu opioid receptor 3620 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Small molecule | Topical: No | First In Class: No | Black Box: No |
| Chirality: No | Availability: No | Prodrug: No |
Drug Indications
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
| Molecular Weight: 350.51 | Molecular Weight (Monoisotopic): 350.2358 | AlogP: 3.59 | #Rotatable Bonds: 6 |
| Polar Surface Area: 15.71 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 8.38 | CX LogP: 4.31 | CX LogD: 3.29 |
| Aromatic Rings: 2 | Heavy Atoms: 26 | QED Weighted: 0.79 | Np 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
Source(1):