N-(4-CHLORO-2-METHYL-6-(2-METHYL-1-(S-METHYLSULFONIMIDOYL)PROPAN-2-YLCARBAMOYL)PHENYL)-1-(3-CHLOROPYRIDIN-2-YL)-3-(TRIFLUOROMETHYL)-1H-PYRAZOLE-5-CARBOXAMIDE


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	PJRXEFAOTDSAFY-UHFFFAOYSA-N
Smiles	Cc1cc(Cl)cc(C(=O)NC(C)(C)CS(=N)(=O)C)c1NC(=O)c2cc(nn2c3ncccc3Cl)C(F)(F)F
InChI	InChI=1S/C23H23Cl2F3N6O3S/c1-12-8-13(24)9-14(20(35)32-22(2,3)11-38(4,29)37)18(12)31-21(36)16-10-17(23(26,27)28)33-34(16)19-15(25)6-5-7-30-19/h5-10,29H,11H2,1-4H3,(H,31,36)(H,32,35)

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C23H23Cl2F3N6O3S
Molecular Weight	591.43
AlogP	5.44
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	3.0
Number of Rotational Bond	8.0
Polar Surface Area	138.21
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	38.0

Assay Description	Organism	Bioactivity
Insecticidal activity against Myzus persicae (green peach aphid) assessed as mortality by greenhouse assay	Myzus persicae	50.0 ppm
Insecticidal activity against Plutella xylostella (diamondback moth) assessed as mortality by greenhouse assay	Plutella xylostella	0.8 ppm
Insecticidal activity against Spodoptera littoralis assessed as mortality by greenhouse assay	Spodoptera littoralis	0.8 ppm
Insecticidal activity against Spodoptera frugiperda (fall armyworm) in maize assessed as control of pests measured after 12 to 22 days of seed application	Spodoptera frugiperda	None
Insecticidal activity against Agrotis ipsilon in maize assessed as control of pests measured after 12 to 22 days of seed application	Agrotis ipsilon	None
Insecticidal activity against Liriomyza trifolii in kidney beans assessed as control of pests measured after 12 to 22 days of seed application	Liriomyza trifolii	None
Insecticidal activity against Phyllotreta striolata in radish assessed as control of pests measured after 12 to 22 days of seed application	Phyllotreta striolata	None
Insecticidal activity against Spodoptera littoralis in maize assessed as control of pests measured after 12 to 22 days of seed application	Spodoptera littoralis	None
Lipophilicity, log P of the compound	None	2.4
Aqueous solubility of the compound at pH 7	None	196.0 ppm
Displacement of [3H]-Tritium-N-(4-chloro-2-methyl-6-(methylcarbamoyl)phenyl)-1-(3-chloropyridin-2-yl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide from Myzus persicae (green peach aphid) ryanodine receptor	Myzus persicae	None
Displacement of [3H]-Tritium-N-(4-chloro-2-methyl-6-(methylcarbamoyl)phenyl)-1-(3-chloropyridin-2-yl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide from Spodoptera littoralis ryanodine receptor	Spodoptera littoralis	None

Cross References

Resources	Reference
ChEMBL	CHEMBL2288194
PubChem	11699907
SureChEMBL	SCHEMBL12870068

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).