4-(3-BROMO-4-FLUOROPHENYL)-6-FLUORO-1H-BENZO[D][1,2]OXAZINE


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	MTXULIDBXBPVHB-UHFFFAOYSA-N
Smiles	Fc1ccc2CON=C(c3ccc(F)c(Br)c3)c2c1
InChI	InChI=1S/C14H8BrF2NO/c15-12-5-8(2-4-13(12)17)14-11-6-10(16)3-1-9(11)7-19-18-14/h1-6H,7H2

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C14H8BrF2NO
Molecular Weight	324.12
AlogP	4.25
Hydrogen Bond Acceptor	2.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	1.0
Polar Surface Area	21.59
Molecular species	None
Aromatic Rings	2.0
Heavy Atoms	19.0

Assay Description	Organism	Bioactivity
Toxicity in Gossypium hirsutum (cotton) assessed as killing at 1 kg/ha by crop selectivity assay	Gossypium hirsutum	0.0 %
Toxicity in Glycine max (soybean) assessed as killing at 1 kg/ha by crop selectivity assay	Glycine max	0.0 %
Toxicity in Triticum aestivum (wheat) plant assessed as killing at 1 kg/ha by crop selectivity assay	Triticum aestivum	2.0 %
Herbicidal activity against Amaranthus viridis assessed as killing at 1 kg/ha	Amaranthus viridis	8.0 %
Herbicidal activity against Digitaria ciliaris assessed as killing at 1 kg/ha	Digitaria ciliaris	10.0 %
Herbicidal activity against Persicaria lapathifolia assessed as killing at 1 kg/ha	Persicaria lapathifolia	6.0 %
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as killing at 1 kg/ha	Echinochloa crus-galli	10.0 %
Toxicity in Gossypium hirsutum (cotton) assessed as killing at 2 kg/ha by crop selectivity assay	Gossypium hirsutum	0.0 %
Toxicity in Triticum aestivum (wheat) plant assessed as killing at 2 kg/ha by crop selectivity assay	Triticum aestivum	20.0 %
Toxicity in Glycine max (soybean) assessed as killing at 2 kg/ha by crop selectivity assay	Glycine max	0.0 %
Herbicidal activity against Amaranthus viridis assessed as killing at 2 kg/ha	Amaranthus viridis	100.0 %
Herbicidal activity against Digitaria ciliaris assessed as killing at 2 kg/ha	Digitaria ciliaris	100.0 %
Herbicidal activity against Persicaria lapathifolia assessed as killing at 2 kg/ha	Persicaria lapathifolia	80.0 %
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as killing at 2 kg/ha	Echinochloa crus-galli	100.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2272563
PubChem	76330697

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).