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 AJYOOHCNOXWTKJ-UHFFFAOYSA-N
Smiles OC(c1ccccc1)c2ccc(Cl)cc2
InChI
InChI=1S/C13H11ClO/c14-12-8-6-11(7-9-12)13(15)10-4-2-1-3-5-10/h1-9,13,15H

Physicochemical Descriptors

Property Name Value
Molecular Formula C13H11ClO
Molecular Weight 218.68
AlogP 3.5
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 2.0
Heavy Atoms 15.0
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 63.0 %
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 87.0 %
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 94.0 %
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 95.0 %
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 CHEMBL2251568
PubChem 8401
SureChEMBL SCHEMBL477379