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ID: ALA2397456
Max Phase: Preclinical
Molecular Formula: C11H7ClN4O3
Molecular Weight: 278.66
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: O=C(Nc1cccc([N+](=O)[O-])c1)c1cnc(Cl)cn1
Standard InChI: InChI=1S/C11H7ClN4O3/c12-10-6-13-9(5-14-10)11(17)15-7-2-1-3-8(4-7)16(18)19/h1-6H,(H,15,17)
Standard InChI Key: WAHMBVUHSWEIEI-UHFFFAOYSA-N
Associated Targets(non-human)
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: 278.66 | Molecular Weight (Monoisotopic): 278.0207 | AlogP: 2.29 | #Rotatable Bonds: 3 |
Polar Surface Area: 98.02 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 12.79 | CX Basic pKa: | CX LogP: 1.78 | CX LogD: 1.78 |
Aromatic Rings: 2 | Heavy Atoms: 19 | QED Weighted: 0.69 | Np Likeness Score: -2.21 |
References
1. Servusová B, Vobicková J, Paterová P, Kubíček V, Kuneš J, Doležal M, Doležal M, Zitko J.. (2013) Synthesis and antimycobacterial evaluation of N-substituted 5-chloropyrazine-2-carboxamides., 23 (12): [PMID:23659859] [10.1016/j.bmcl.2013.04.021] |