| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA221898
Max Phase: Preclinical
Molecular Formula: C20H22N4
Molecular Weight: 318.42
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: C#Cc1ccc(N2CCN(CC3C=NN4C=CC=CC34)CC2)cc1
Standard InChI: InChI=1S/C20H22N4/c1-2-17-6-8-19(9-7-17)23-13-11-22(12-14-23)16-18-15-21-24-10-4-3-5-20(18)24/h1,3-10,15,18,20H,11-14,16H2
Standard InChI Key: AREIGLVVBYCXNP-UHFFFAOYSA-N
Associated Targets(Human)
Dopamine receptors; D2 & D3 635 Activities
Dopamine receptors; D3 & D4 312 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: 318.42 | Molecular Weight (Monoisotopic): 318.1844 | AlogP: 2.16 | #Rotatable Bonds: 3 |
| Polar Surface Area: 22.08 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 8.21 | CX LogP: 2.01 | CX LogD: 1.14 |
| Aromatic Rings: 1 | Heavy Atoms: 24 | QED Weighted: 0.80 | Np Likeness Score: -0.92 |
References
| 1. Salama I, Hocke C, Utz W, Prante O, Boeckler F, Hübner H, Kuwert T, Gmeiner P.. (2007) Structure-selectivity investigations of D2-like receptor ligands by CoMFA and CoMSIA guiding the discovery of D3 selective PET radioligands., 50 (3): [PMID:17266201] [10.1021/jm0611152] |
Source
Source(1):