5-(4-CHLOROPHENYL)-3-(3-(2,6-DICHLORO-4-(3,3-DICHLOROALLYLOXY)PHENOXY)PROPOXY)-1,4-DIMETHYL-1H-PYRAZOLE


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	QMSIHKIWEUQXED-UHFFFAOYSA-N
Smiles	Cc1c(OCCCOc2c(Cl)cc(OCC=C(Cl)Cl)cc2Cl)nn(C)c1c3ccc(Cl)cc3
InChI	InChI=1S/C23H21Cl5N2O3/c1-14-21(15-4-6-16(24)7-5-15)30(2)29-23(14)33-10-3-9-32-22-18(25)12-17(13-19(22)26)31-11-8-20(27)28/h4-8,12-13H,3,9-11H2,1-2H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C23H21Cl5N2O3
Molecular Weight	550.69
AlogP	8.33
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	10.0
Polar Surface Area	45.51
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	33.0

Assay Description	Organism	Bioactivity
Insecticidal activity against third-instar larvae of Plutella xylostella (diamondback moth) fed on compound treated cabbage leaves assessed as mortality at 6.25 mg/l after 3 days relative to control	Plutella xylostella	20.0 %
Insecticidal activity against third-instar larvae of Plutella xylostella (diamondback moth) fed on compound treated cabbage leaves assessed as mortality at 25 mg/l after 3 days relative to control	Plutella xylostella	50.0 %
Insecticidal activity against third-instar larvae of Plutella xylostella (diamondback moth) fed on compound treated cabbage leaves assessed as mortality at 100 mg/l after 3 days relative to control	Plutella xylostella	80.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2288627
PubChem	76334717

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).