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 CLKPSDBTSRWVOQ-UHFFFAOYSA-N
Smiles OC(C1CC1)c2ccc(Cl)cc2
InChI
InChI=1S/C10H11ClO/c11-9-5-3-8(4-6-9)10(12)7-1-2-7/h3-7,10,12H,1-2H2

Physicochemical Descriptors

Property Name Value
Molecular Formula C10H11ClO
Molecular Weight 182.65
AlogP 2.74
Hydrogen Bond Acceptor 1.0
Hydrogen Bond Donor 1.0
Number of Rotational Bond 2.0
Polar Surface Area 20.23
Molecular species NEUTRAL
Aromatic Rings 1.0
Heavy Atoms 12.0
Assay Description Organism Bioactivity Reference
Antifungal activity against Colletotrichum gloeosporioides 20122-CECT assessed as inhibition of radial growth at 50 ug/mL at 25 degC measured after 5 days Colletotrichum gloeosporioides 31.0 %
Antifungal activity against Colletotrichum gloeosporioides 20122-CECT assessed as inhibition of radial growth at 100 ug/mL at 25 degC measured after 5 days Colletotrichum gloeosporioides 53.0 %
Antifungal activity against Colletotrichum gloeosporioides 20122-CECT assessed as inhibition of radial growth at 150 ug/mL at 25 degC measured after 5 days Colletotrichum gloeosporioides 80.0 %
Antifungal activity against Botryotinia fuckeliana 2100 assessed as inhibition of radial growth at 50 ug/mL at 25 degC measured after 5 days Botryotinia fuckeliana 74.0 %
Antifungal activity against Botryotinia fuckeliana 2100 assessed as inhibition of radial growth at 100 ug/mL at 25 degC measured after 5 days Botryotinia fuckeliana 100.0 %
Antifungal activity against Botryotinia fuckeliana 2100 assessed as inhibition of radial growth at 150 ug/mL at 25 degC measured after 5 days Botryotinia fuckeliana 100.0 %

Cross References

Resources Reference
ChEMBL CHEMBL2251576
PubChem 86679
SureChEMBL SCHEMBL1349046