ID: ALA4160244
Chembl Id: CHEMBL4160244
PubChem CID: 145956904
Max Phase: Preclinical
Molecular Formula: C19H16N4O
Molecular Weight: 316.36
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: COc1ccc(-c2nc3nnccn3c2-c2ccccc2C)cc1
Standard InChI: InChI=1S/C19H16N4O/c1-13-5-3-4-6-16(13)18-17(14-7-9-15(24-2)10-8-14)21-19-22-20-11-12-23(18)19/h3-12H,1-2H3
Standard InChI Key: ZBGFLCZQZBXRBR-UHFFFAOYSA-N
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| 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 |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| Molecular Weight: 316.36 | Molecular Weight (Monoisotopic): 316.1324 | AlogP: 3.78 | #Rotatable Bonds: 3 |
| Polar Surface Area: 52.31 | Molecular Species: NEUTRAL | HBA: 5 | HBD: ┄ |
| #RO5 Violations: ┄ | HBA (Lipinski): 5 | HBD (Lipinski): ┄ | #RO5 Violations (Lipinski): ┄ |
| CX Acidic pKa: ┄ | CX Basic pKa: ┄ | CX LogP: 2.78 | CX LogD: 2.78 |
| Aromatic Rings: 4 | Heavy Atoms: 24 | QED Weighted: 0.58 | Np Likeness Score: -1.16 |
| 1. Loubidi M, Jouha J, Tber Z, Khouili M, Suzenet F, Akssira M, Erdogan MA, Köse FA, Dagcı T, Armagan G, Saso L, Guillaumet G.. (2018) Efficient synthesis and first regioselective C-6 direct arylation of imidazo[2,1-c][1,2,4]triazine scaffold and their evaluation in H2O2-induced oxidative stress., 145 [PMID:29324335] [10.1016/j.ejmech.2017.12.081] |
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