| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA2431036
Max Phase: Preclinical
Molecular Formula: C20H30ClN3O3
Molecular Weight: 359.47
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Cc1cccc(OCCNCCCCN2C(=O)C3CCCN3C2=O)c1C.Cl
Standard InChI: InChI=1S/C20H29N3O3.ClH/c1-15-7-5-9-18(16(15)2)26-14-11-21-10-3-4-12-23-19(24)17-8-6-13-22(17)20(23)25;/h5,7,9,17,21H,3-4,6,8,10-14H2,1-2H3;1H
Standard InChI Key: GQUMYDSHDGDFBW-UHFFFAOYSA-N
Associated Targets(non-human)
Serotonin 7 (5-HT7) receptor 811 Activities
Serotonin 4 (5-HT4) receptor 653 Activities
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Serotonin 3a (5-HT3a) receptor 173 Activities
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Serotonin 2a (5-HT2a) receptor 3540 Activities
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Serotonin 1a (5-HT1a) receptor 8655 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 |
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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: 359.47 | Molecular Weight (Monoisotopic): 359.2209 | AlogP: 2.48 | #Rotatable Bonds: 9 |
| Polar Surface Area: 61.88 | Molecular Species: BASE | HBA: 4 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 13.50 | CX Basic pKa: 9.46 | CX LogP: 2.50 | CX LogD: 0.46 |
| Aromatic Rings: 1 | Heavy Atoms: 26 | QED Weighted: 0.54 | Np Likeness Score: -0.94 |
References
| 1. Valhondo M, Marco I, Martín-Fontecha M, Vázquez-Villa H, Ramos JA, Berkels R, Lauterbach T, Benhamú B, López-Rodríguez ML.. (2013) New serotonin 5-HT1A receptor agonists endowed with antinociceptive activity in vivo., 56 (20): [PMID:24050112] [10.1021/jm400766k] |
Source
Source(1):