S-4-(1,3-DIOXOISOINDOLIN-2-YL)BUTYL O,O-DIETHYL PHOSPHOROTHIOATE


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	ZCPLATPMENEVQQ-UHFFFAOYSA-N
Smiles	CCOP(=O)(OCC)SCCCCN1C(=O)c2ccccc2C1=O
InChI	InChI=1S/C16H22NO5PS/c1-3-21-23(20,22-4-2)24-12-8-7-11-17-15(18)13-9-5-6-10-14(13)16(17)19/h5-6,9-10H,3-4,7-8,11-12H2,1-2H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C16H22NO5PS
Molecular Weight	371.39
AlogP	2.41
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	10.0
Polar Surface Area	108.02
Molecular species	NEUTRAL
Aromatic Rings	1.0
Heavy Atoms	24.0

Assay Description	Organism	Bioactivity
Insecticidal activity against Lipaphis erysimi (mustard aphids) assessed as insect mortality at 300 mg/mL	Lipaphis erysimi	97.7 %
Insecticidal activity against Tetranychus cinnabarinus (carmine spider mite) assessed as insect mortality at 300 mg/mL	Tetranychus cinnabarinus	88.9 %
Inhibition of acetylcholinesterase in Musca domestica (house fly) brain by Ellman's method	Musca domestica	25770.0 nM
Inhibition of acetylcholinesterase in Drosophila melanogaster brain by Ellman's method	Drosophila melanogaster	9920.0 nM

Cross References

Resources	Reference
ChEMBL	CHEMBL2252848
PubChem	76333655

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).