N-(3-FLUOROPHENYL)-N-METHYL-2-(4-METHYL-3-(TRIFLUOROMETHYL)ISOXAZOL-5-YLOXY)ACETAMIDE


Source	Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...


Active Pharmaceutical Ingredients Bioactive chemicals	Exact Similarity SubStructure	Threshold (%) >= 70

Structure


InChI Key	VSACSSUSBNBFBM-UHFFFAOYSA-N
Smiles	CN(C(=O)COc1onc(c1C)C(F)(F)F)c2cccc(F)c2
InChI	InChI=1S/C14H12F4N2O3/c1-8-12(14(16,17)18)19-23-13(8)22-7-11(21)20(2)10-5-3-4-9(15)6-10/h3-6H,7H2,1-2H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C14H12F4N2O3
Molecular Weight	332.25
AlogP	3.3
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	5.0
Polar Surface Area	55.57
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	23.0

Assay Description	Organism	Bioactivity
Toxicity in Gossypium hirsutum cv. Hakushuu (cotton) assessed as seedling death under green house at 0.25 kg/ha at 25 degC measured after 4 weeks by crop selectivity assay	Gossypium hirsutum	None
Toxicity in Glycine max cv. Tamahomare (soybean) assessed as seedling death under green house at 0.25 kg/ha at 25 degC measured after 4 weeks by crop selectivity assay	Glycine max	None
Herbicidal activity against Amaranthus viridis assessed as seedling death under green house at 0.25 kg/ha at 25 degC measured after 4 weeks	Amaranthus viridis	None
Toxicity in Triticum aestivum cv. Nohrin-61 (wheat) assessed as seedling death under green house at 0.25 kg/ha at 25 degC measured after 4 weeks by crop selectivity assay	Triticum aestivum	None
Herbicidal activity against Digitaria ciliaris assessed as seedling death under green house at 0.25 kg/ha at 25 degC measured after 4 weeks	Digitaria ciliaris	None
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as seedling death under green house at 0.25 kg/ha at 25 degC measured after 4 weeks	Echinochloa crus-galli	None
Herbicidal activity against Amaranthus viridis assessed as seedling death under green house at 0.5 kg/ha at 25 degC measured after 4 weeks	Amaranthus viridis	None
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as seedling death under green house at 0.5 kg/ha at 25 degC measured after 4 weeks	Echinochloa crus-galli	None
Herbicidal activity against Digitaria ciliaris assessed as seedling death under green house at 0.5 kg/ha at 25 degC measured after 4 weeks	Digitaria ciliaris	None
Herbicidal activity against Amaranthus viridis assessed as seedling death under green house at 1 kg/ha at 25 degC measured after 4 weeks	Amaranthus viridis	None
Herbicidal activity against Persicaria lapathifolia assessed as seedling death under green house at 1 kg/ha at 25 degC measured after 4 weeks	Persicaria lapathifolia	None
Herbicidal activity against Digitaria ciliaris assessed as seedling death under green house at 1 kg/ha at 25 degC measured after 4 weeks	Digitaria ciliaris	None
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as seedling death under green house at 1 kg/ha at 25 degC measured after 4 weeks	Echinochloa crus-galli	None

Cross References

Resources	Reference
ChEMBL	CHEMBL2287930
PubChem	14855525

CONTENTS


PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).