6-(ISOBUTYLTHIO)PYRIDIN-2-YL METHANESULFONATE

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Search structure


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	BBPAPSVFSDRUHU-UHFFFAOYSA-N
Smiles	CC(C)CSc1cccc(OS(=O)(=O)C)n1
InChI	InChI=1S/C10H15NO3S2/c1-8(2)7-15-10-6-4-5-9(11-10)14-16(3,12)13/h4-6,8H,7H2,1-3H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C10H15NO3S2
Molecular Weight	261.36
AlogP	3.05
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	5.0
Polar Surface Area	89.94
Molecular species	NEUTRAL
Aromatic Rings	1.0
Heavy Atoms	16.0

Assay Description	Organism	Bioactivity	Reference
Methanol-water partition coefficient, log k of the compound	None	0.399
Insecticidal activity against resistant Nephotettix cincticeps Izumi (green rice leafhopper) assessed as mortality by foliar-spray	Nephotettix cincticeps	7.95
Insecticidal activity against susceptible Nephotettix cincticeps Ageo (green rice leafhopper)assessed as mortality by foliar-spray	Nephotettix cincticeps	8.16
Insecticidal activity against Musca domestica (house fly) NAIDM	Musca domestica	1.11 ug
Insecticidal activity against drug-susceptible Nephotettix cincticeps Ageo (green rice leafhopper) assessed as mortality after 2 days by foliar spraying method	Nephotettix cincticeps	1.06 mg.kg-1
Inhibition of Bos taurus (bovine) erythrocytes acetylcholinesterase	Bos taurus	2000000.0 nM
Inhibition of Musca domestica (house fly) NAIDM head acetylcholinesterase	Musca domestica	1300000.0 nM
Lipophilicity, log K of the compound	None	0.4
Inhibition of drug-susceptible Nephotettix cincticeps Ageo (green rice leafhopper) acetylcholinesterase	Nephotettix cincticeps	2000000.0 nM
Insecticidal activity against drug-resistant Nephotettix cincticeps Izumi (green rice leafhopper) assessed as mortality at 200 ppm after 2 days by foliar spraying method	Nephotettix cincticeps	2.9 mg.kg-1
Insecticidal activity against drug-susceptible Nephotettix cincticeps Ageo (green rice leafhopper) assessed as mortality at 200 ppm after 2 days by foliar spraying method	Nephotettix cincticeps	1.8 mg.kg-1
Acaricidal activity against Tetranychus urticae (two-spotted spider mite) assessed as mortality at 200 ppm after 2 days by leaf dipping method	Tetranychus urticae	72.0 %
Drug degradation in sorensen buffer assessed as hydrolysis at 3 x 10'-5 M at pH 7.4 after 24 hr	None	1.8 %
Insecticidal activity against Culex pipiens assessed as mortality at 200 ppm after 2 days by immersion method	Culex pipiens	100.0 %
Insecticidal activity against Plutella xylostella (diamondback moth) assessed as mortality at 200 ppm after 2 days by foliar spraying method	Plutella xylostella	0.0 %
Insecticidal activity against Nilaparvata lugens (brown planthopper) assessed as mortality at 200 ppm after 2 days by foliar spraying method	Nilaparvata lugens	100.0 %
Insecticidal activity against Nephotettix cincticeps Izumi (green rice leafhopper) assessed as mortality at 200 ppm after 2 days by foliar spraying method	Nephotettix cincticeps	100.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2286245
PubChem	13748732

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).