ID: ALA3408294
Chembl Id: CHEMBL3408294
PubChem CID: 89964926
Max Phase: Preclinical
Molecular Formula: C15H21ClN2
Molecular Weight: 228.34
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: Cc1ccc(/N=C2/CC(C)CN2)c2c1CCC2.Cl
Standard InChI: InChI=1S/C15H20N2.ClH/c1-10-8-15(16-9-10)17-14-7-6-11(2)12-4-3-5-13(12)14;/h6-7,10H,3-5,8-9H2,1-2H3,(H,16,17);1H
Standard InChI Key: BBTPWUDIUFTVPM-UHFFFAOYSA-N
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| 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 |
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
|---|
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
| Molecular Weight: 228.34 | Molecular Weight (Monoisotopic): 228.1626 | AlogP: 3.33 | #Rotatable Bonds: 1 |
| Polar Surface Area: 24.39 | Molecular Species: BASE | HBA: 2 | HBD: 1 |
| #RO5 Violations: ┄ | HBA (Lipinski): 2 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): ┄ |
| CX Acidic pKa: ┄ | CX Basic pKa: 8.86 | CX LogP: 3.56 | CX LogD: 2.13 |
| Aromatic Rings: 1 | Heavy Atoms: 17 | QED Weighted: 0.78 | Np Likeness Score: -0.10 |
| 1. Gasparik V, Greney H, Schann S, Feldman J, Fellmann L, Ehrhardt JD, Bousquet P.. (2015) Synthesis and biological evaluation of 2-aryliminopyrrolidines as selective ligands for I1 imidazoline receptors: discovery of new sympatho-inhibitory hypotensive agents with potential beneficial effects in metabolic syndrome., 58 (2): [PMID:25521963] [10.1021/jm501456p] |
Source(1):
