Synonyms
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 QYKQWFZDEDFELK-UHFFFAOYSA-N
Smiles CSC(=S)NCc1c[nH]c2ccccc12
InChI
InChI=1S/C11H12N2S2/c1-15-11(14)13-7-8-6-12-10-5-3-2-4-9(8)10/h2-6,12H,7H2,1H3,(H,13,14)

Physicochemical Descriptors

Property Name Value
Molecular Formula C11H12N2S2
Molecular Weight 236.36
AlogP 3.55
Hydrogen Bond Acceptor 2.0
Hydrogen Bond Donor 2.0
Number of Rotational Bond 4.0
Polar Surface Area 85.21
Molecular species NEUTRAL
Aromatic Rings 2.0
Heavy Atoms 15.0
Assay Description Organism Bioactivity Reference
Drug metabolism in Leptosphaeria maculans isolate BJ-125 assessed as rate of transformation to indole-3-carboxaldehyde at 0.10 mM after 15 hr by HPLC analysis Leptosphaeria maculans 40.0 %
Drug metabolism in Leptosphaeria maculans isolate BJ-125 assessed as drug recovery at 0.10 mM after 24 hr by HPLC analysis Leptosphaeria maculans 5.0 %
Antifungal activity against Leptosphaeria maculans isolate BJ-125/UAMH-9410 assessed as mycelial growth inhibition at 0.1 mM incubated under constant light for 5 days by mycelial radial growth bioassay Leptosphaeria maculans 10.0 %
Antifungal activity against Leptosphaeria maculans isolate BJ-125/UAMH-9410 assessed as mycelial growth inhibition at 0.2 mM incubated under constant light for 5 days by mycelial radial growth bioassay Leptosphaeria maculans 21.0 %
Antifungal activity against Leptosphaeria maculans isolate BJ-125/UAMH-9410 assessed as mycelial growth inhibition at 0.5 mM incubated under constant light for 5 days by mycelial radial growth bioassay Leptosphaeria maculans 55.0 %

Cross References

Resources Reference
ChEMBL CHEMBL373777
PubChem 3035211
SureChEMBL SCHEMBL849773
ZINC ZINC02382836