4-(3-CYANOHEXAN-3-YLCARBAMOYL)-1-METHYL-1H-PYRAZOL-3-YL METHANESULFONATE


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	RQDJGBKQQVIDBC-UHFFFAOYSA-N
Smiles	CCCC(CC)(NC(=O)c1cn(C)nc1OS(=O)(=O)C)C#N
InChI	InChI=1S/C13H20N4O4S/c1-5-7-13(6-2,9-14)15-11(18)10-8-17(3)16-12(10)21-22(4,19)20/h8H,5-7H2,1-4H3,(H,15,18)

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C13H20N4O4S
Molecular Weight	328.39
AlogP	1.82
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	7.0
Polar Surface Area	122.46
Molecular species	NEUTRAL
Aromatic Rings	1.0
Heavy Atoms	22.0

Assay Description	Organism	Bioactivity
Insecticidal activity against Tetranychus urticae (two-spotted spider mite) eggs in compound treated kidney bean leaf disk assessed as ovicidal at 62.5 ppm measured after 7 days	Tetranychus urticae	39.0 %
Insecticidal activity against Tetranychus urticae (two-spotted spider mite) in compound treated kidney bean leaf disk assessed as mortality at 62.5 ppm measured after 7 days	Tetranychus urticae	15.0 %
Insecticidal activity against Nephotettix cincticeps (green rice leafhopper) third instar larvae in compound treated rice seedlings assessed as mortality at 62.5 ppm measured after 7 days	Nephotettix cincticeps	22.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2271622
PubChem	76312521

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).