2-TERT-BUTYL-4-CHLORO-5-((5-(2,4-DICHLORO-5-FLUOROPHENYL)-1,3,4-OXADIAZOL-2-YL)METHOXY)PYRIDAZIN-3(2H)-ONE


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	CCTIKIMGVAIECA-UHFFFAOYSA-N
Smiles	CC(C)(C)N1N=CC(=C(Cl)C1=O)OCc2oc(nn2)c3cc(F)c(Cl)cc3Cl
InChI	InChI=1S/C17H14Cl3FN4O3/c1-17(2,3)25-16(26)14(20)12(6-22-25)27-7-13-23-24-15(28-13)8-4-11(21)10(19)5-9(8)18/h4-6H,7H2,1-3H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C17H14Cl3FN4O3
Molecular Weight	447.68
AlogP	3.5
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	5.0
Polar Surface Area	80.82
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	28.0

Assay Description	Organism	Bioactivity
Hydrophobicity, log P of the compound	None	3.36
Antifeedant activity against second-instar larvae of Mythimna separata (Oriental armyworm) in compound treated leaves assessed as growth inhibition measured after 5 days by chronic growth bioassay	Mythimna separata	23120.65 nM	Antifeedant activity against second-instar larvae of Mythimna separata (Oriental armyworm) in compound treated leaves assessed as growth inhibition measured after 5 days by chronic growth bioassay	Mythimna separata	23.1 ug.mL-1
Antifeedant activity against fifth-instar larval stage of Ostrinia furnacalis (Asian corn borer) assessed as feeding deterrence index at 500 mg/kg after 24 hr by diet-choice assay	Ostrinia furnacalis	35.16 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2252408
PubChem	10884819

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).