METHYL 3-(6-(2-CHLORO-6-FLUORO-4-(TRIFLUOROMETHYL)PHENOXY)-1H-BENZO[D][1,2,3]TRIAZOL-1-YL)PROPANOATE


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	MRKQQGMTDZQANQ-UHFFFAOYSA-N
Smiles	COC(=O)CCn1nnc2ccc(Oc3c(F)cc(cc3Cl)C(F)(F)F)cc12
InChI	InChI=1S/C17H12ClF4N3O3/c1-27-15(26)4-5-25-14-8-10(2-3-13(14)23-24-25)28-16-11(18)6-9(7-12(16)19)17(20,21)22/h2-3,6-8H,4-5H2,1H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C17H12ClF4N3O3
Molecular Weight	417.74
AlogP	4.97
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	7.0
Polar Surface Area	66.24
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	28.0

Assay Description	Organism	Bioactivity
Post-emergence herbicidal activity against Digitaria sanguinalis (hairy crabgrass)	Digitaria sanguinalis	32.0 g/ha
Post-emergence herbicidal activity against Echinochloa crus-galli (barnyard grass)	Echinochloa crus-galli	125.0 g/ha
Post-emergence herbicidal activity against Setaria viridis (green foxtail)	Setaria viridis	250.0 g/ha
Post-emergence herbicidal activity against Ipomoea purpurea (common morning-glory)	Ipomoea purpurea	32.0 g/ha
Post-emergence herbicidal activity against Abutilon theophrasti (velvetleaf)	Abutilon theophrasti	32.0 g/ha

Cross References

Resources	Reference
ChEMBL	CHEMBL2287031
PubChem	76331022

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).