| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA2235131
Max Phase: Preclinical
Molecular Formula: C8H8Cl2N2
Molecular Weight: 203.07
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: N/N=C/Cc1ccc(Cl)cc1Cl
Standard InChI: InChI=1S/C8H8Cl2N2/c9-7-2-1-6(3-4-12-11)8(10)5-7/h1-2,4-5H,3,11H2/b12-4+
Standard InChI Key: AQHRZDBZBINLEJ-UUILKARUSA-N
Associated Targets(Human)
Gamma-amino-N-butyrate transaminase 140 Activities
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 |
|---|
Properties
| Molecular Weight: 203.07 | Molecular Weight (Monoisotopic): 202.0065 | AlogP: 2.48 | #Rotatable Bonds: 2 |
| Polar Surface Area: 38.38 | Molecular Species: NEUTRAL | HBA: 2 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 2 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 2.48 | CX LogP: 2.38 | CX LogD: 2.38 |
| Aromatic Rings: 1 | Heavy Atoms: 12 | QED Weighted: 0.45 | Np Likeness Score: -0.87 |
References
| 1. Bansal SK, Sinha BN, Khosa RL, Olson AJ. (2011) Novel GABA-AT inhibitors: QSAR and docking based virtual screening of phenyl substituted -phenyl ethylidene hydrazine analogues, 20 (9): [10.1007/s00044-010-9390-6] |
Source
Source(1):