3-BROMO-1-(3-CHLOROPYRIDIN-2-YL)-N-(4-IODOPHENYL)-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	ZPEQKSSVNOBVPK-UHFFFAOYSA-N
Smiles	Clc1cccnc1n2nc(Br)cc2C(=O)Nc3ccc(I)cc3
InChI	InChI=1S/C15H9BrClIN4O/c16-13-8-12(15(23)20-10-5-3-9(18)4-6-10)22(21-13)14-11(17)2-1-7-19-14/h1-8H,(H,20,23)

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C15H9BrClIN4O
Molecular Weight	503.52
AlogP	4.75
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	3.0
Polar Surface Area	59.81
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	23.0

Assay Description	Organism	Bioactivity
Insecticidal activity against Culex pipiens pallens (mosquito) fourth-instar larvae assessed as mortality at 2 ug/mL measured 72 hr post compound treatment	Culex pipiens pallens	100.0 %
Insecticidal activity against fourth-instar larvae of Mythimna separata (Oriental armyworm) reared on compound pre-treated corn leaves assessed as mortality at 50 ug/mL measured 72 hr post compound treatment by leaf-dipping assay	Mythimna separata	50.0 %
Insecticidal activity against fourth-instar larvae of Mythimna separata (Oriental armyworm) reared on compound pre-treated corn leaves assessed as mortality at 100 ug/mL measured 72 hr post compound treatment by leaf-dipping assay	Mythimna separata	100.0 %
Insecticidal activity against fourth-instar larvae of Mythimna separata (Oriental armyworm) reared on compound pre-treated corn leaves assessed as mortality at 200 ug/mL measured 72 hr post compound treatment by leaf-dipping assay	Mythimna separata	100.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2253182
PubChem	76326398

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).