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 UZHJYSOPDZKFIJ-XDHOZWIPSA-N
Smiles COc1ccccc1\C(=N\Nc2nc3c(C)cccc3s2)\C
InChI
InChI=1S/C17H17N3OS/c1-11-7-6-10-15-16(11)18-17(22-15)20-19-12(2)13-8-4-5-9-14(13)21-3/h4-10H,1-3H3,(H,18,20)/b19-12+

Physicochemical Descriptors

Property Name Value
Molecular Formula C17H17N3OS
Molecular Weight 311.4
AlogP 4.52
Hydrogen Bond Acceptor 4.0
Hydrogen Bond Donor 1.0
Number of Rotational Bond 4.0
Polar Surface Area 74.75
Molecular species NEUTRAL
Aromatic Rings 3.0
Heavy Atoms 22.0
Assay Description Organism Bioactivity Reference
Fungicidal activity against Rhizoctonia solani assessed as inhibition rate of circle mycelium growth at 500 ug/ml Rhizoctonia solani 60.0 %
Fungicidal activity against Ustilaginoidea oryzae assessed as inhibition rate of circle mycelium growth at 500 ug/ml Ustilaginoidea 0.0 %
Fungicidal activity against Alternaria alternata assessed as inhibition rate of circle mycelium growth at 500 ug/ml Alternaria alternata 0.0 %
Fungicidal activity against Phytophthora capsici assessed as inhibition rate of circle mycelium growth at 500 ug/ml Phytophthora capsici 0.0 %
Fungicidal activity against Fusarium graminearum assessed as inhibition rate of circle mycelium growth at 500 ug/ml Fusarium graminearum 0.0 %
Fungicidal activity against Botryotinia fuckeliana assessed as inhibition rate of circle mycelium growth at 500 ug/ml Botryotinia fuckeliana 0.0 %
Fungicidal activity against Sclerotinia sclerotiorum assessed as inhibition rate of circle mycelium growth at 500 ug/ml Sclerotinia sclerotiorum 3.1 %

Cross References

Resources Reference
ChEMBL CHEMBL2268716
PubChem 76323173