UNII G3LOM1T4X9
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 ...

Structure

InChI Key ICTQUFQQEYSGGJ-UHFFFAOYSA-N
Smiles CN(C)C1CSSSC1.OC(=O)C(=O)O
InChI
InChI=1S/C5H11NS3.C2H2O4/c1-6(2)5-3-7-9-8-4-5;3-1(4)2(5)6/h5H,3-4H2,1-2H3;(H,3,4)(H,5,6)

Physicochemical Descriptors

Property Name Value
Molecular Formula C7H13NO4S3
Molecular Weight 271.38
AlogP 1.96
Hydrogen Bond Acceptor 4.0
Hydrogen Bond Donor 0.0
Number of Rotational Bond 1.0
Polar Surface Area 79.14
Molecular species NEUTRAL
Aromatic Rings 0.0
Heavy Atoms 9.0
Assay Description Organism Bioactivity Reference
Acaricidal activity against Tetranychus urticae (two-spotted spider mite) assessed as mortality at 500 ppm Tetranychus urticae 80.0 %
Insecticidal activity against Chilo suppressalis (rice stem borer) assessed as mortality at 50 ug/g administered as topical application Chilo suppressalis 100.0 %
Insecticidal activity against Spodoptera litura assessed as mortality at 500 ppm Spodoptera litura 20.0 %
Insecticidal activity against Nilaparvata lugens (brown planthopper) assessed as mortality at 50 ppm Nilaparvata lugens 100.0 %
Insecticidal activity against Culex pipiens molestus assessed as mortality at 5 ppm Culex pipiens molestus 100.0 %
Ratio of EC50 for Daphnia magna to EC50 for first instar larvae of Cheumatopsyche brevilineata None 2.54
Insecticidal activity against first-instar larvae of Cheumatopsyche brevilineata after 48 hr Cheumatopsyche 0.00576 ug.mL-1
Octanol-water partition coefficient, log KOW of the compound None -0.07
Insecticidal activity against Daphnia pulex after 48 hr Daphnia pulex 2.01 ug.mL-1

Cross References

Resources Reference
ChEMBL CHEMBL2270412
FDA SRS G3LOM1T4X9
PubChem 35969
SureChEMBL SCHEMBL143310