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ID: ALA2253299
Max Phase: Preclinical
Molecular Formula: C18H13F4N3
Molecular Weight: 347.31
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Cc1cc(-c2cccc(C(F)(F)F)c2)c(Nc2ccc(F)cc2)nn1
Standard InChI: InChI=1S/C18H13F4N3/c1-11-9-16(12-3-2-4-13(10-12)18(20,21)22)17(25-24-11)23-15-7-5-14(19)6-8-15/h2-10H,1H3,(H,23,25)
Standard InChI Key: JECJPKPQCUXRRK-UHFFFAOYSA-N
Associated Targets(non-human)
Spirodela polyrhiza 146 Activities
Amaranthus retroflexus 1838 Activities
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Brassica rapa subsp. oleifera 1696 Activities
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Digitaria 171 Activities
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Echinochloa crus-galli 3685 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: 347.31 | Molecular Weight (Monoisotopic): 347.1046 | AlogP: 5.35 | #Rotatable Bonds: 3 |
| Polar Surface Area: 37.81 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 1 |
| #RO5 Violations: 1 | HBA (Lipinski): 3 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: | CX Basic pKa: 4.04 | CX LogP: 4.61 | CX LogD: 4.61 |
| Aromatic Rings: 3 | Heavy Atoms: 25 | QED Weighted: 0.65 | Np Likeness Score: -1.49 |
References
| 1. Xu H, Hu XH, Zou XM, Liu B, Zhu YQ, Wang Y, Hu FZ, Yang HZ.. (2008) Synthesis and herbicidal activities of novel 3-N-substituted amino-6-methyl-4-(3-trifluoromethylphenyl)pyridazine derivatives., 56 (15): [PMID:18605735] [10.1021/jf800900h] |
Source
Source(1):