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ID: ALA2287767
Max Phase: Preclinical
Molecular Formula: C24H17F3N2O
Molecular Weight: 406.41
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Cc1cc(-c2cccc(C(F)(F)F)c2)c(Oc2ccccc2-c2ccccc2)nn1
Standard InChI: InChI=1S/C24H17F3N2O/c1-16-14-21(18-10-7-11-19(15-18)24(25,26)27)23(29-28-16)30-22-13-6-5-12-20(22)17-8-3-2-4-9-17/h2-15H,1H3
Standard InChI Key: JIPVFHCDSUBFJC-UHFFFAOYSA-N
Associated Targets(non-human)
Digitaria 171 Activities
Echinochloa crus-galli 3685 Activities
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Amaranthus retroflexus 1838 Activities
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Brassica rapa subsp. oleifera 1696 Activities
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Spirodela polyrhiza 146 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
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Mechanisms of Action
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Properties
| Molecular Weight: 406.41 | Molecular Weight (Monoisotopic): 406.1293 | AlogP: 6.93 | #Rotatable Bonds: 4 |
| Polar Surface Area: 35.01 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 0 |
| #RO5 Violations: 1 | HBA (Lipinski): 3 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: | CX Basic pKa: 2.54 | CX LogP: 6.17 | CX LogD: 6.17 |
| Aromatic Rings: 4 | Heavy Atoms: 30 | QED Weighted: 0.37 | Np Likeness Score: -0.91 |
References
| 1. Xu H, Zhu YQ, Zou XM, Liu B, Wang Y, Hu FZ, Yang HZ.. (2012) Synthesis and herbicidal activities of novel 3-(substituted benzyloxy or phenoxy)-6-methyl-4-(3-trifluoromethylphenyl)pyridazine derivatives., 68 (2): [PMID:22076665] [10.1002/ps.2257] |
Source
Source(1):