| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA2431054
Max Phase: Preclinical
Molecular Formula: C18H25BrClN3O3
Molecular Weight: 410.31
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Cl.O=C1C2CCCN2C(=O)N1CCCCNCCOc1cccc(Br)c1
Standard InChI: InChI=1S/C18H24BrN3O3.ClH/c19-14-5-3-6-15(13-14)25-12-9-20-8-1-2-10-22-17(23)16-7-4-11-21(16)18(22)24;/h3,5-6,13,16,20H,1-2,4,7-12H2;1H
Standard InChI Key: SUYTYQKZLIMSJU-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: 410.31 | Molecular Weight (Monoisotopic): 409.1001 | AlogP: 2.62 | #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: 9.43 | CX LogP: 2.24 | CX LogD: 0.23 |
| Aromatic Rings: 1 | Heavy Atoms: 25 | QED Weighted: 0.50 | Np Likeness Score: -1.06 |
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):