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ID: ALA2413972
Max Phase: Preclinical
Molecular Formula: C13H12N2O5
Molecular Weight: 276.25
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: COC(=O)c1ccc2c(c1)[n+]([O-])c(C(C)=O)c(C)[n+]2[O-]
Standard InChI: InChI=1S/C13H12N2O5/c1-7-12(8(2)16)15(19)11-6-9(13(17)20-3)4-5-10(11)14(7)18/h4-6H,1-3H3
Standard InChI Key: XJWWXAFSESUFPL-UHFFFAOYSA-N
Associated Targets(non-human)
Vero 26788 Activities
Entamoeba histolytica 2676 Activities
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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: 276.25 | Molecular Weight (Monoisotopic): 276.0746 | AlogP: 0.40 | #Rotatable Bonds: 2 |
| Polar Surface Area: 97.25 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 12.24 | CX Basic pKa: 0.73 | CX LogP: -0.72 | CX LogD: -0.72 |
| Aromatic Rings: 2 | Heavy Atoms: 20 | QED Weighted: 0.34 | Np Likeness Score: -0.13 |
References
| 1. Duque-Montaño BE, Gómez-Caro LC, Sanchez-Sanchez M, Monge A, Hernández-Baltazar E, Rivera G, Torres-Angeles O.. (2013) Synthesis and in vitro evaluation of new ethyl and methyl quinoxaline-7-carboxylate 1,4-di-N-oxide against Entamoeba histolytica., 21 (15): [PMID:23787289] [10.1016/j.bmc.2013.05.036] |
Source
Source(1):