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 AWZJRRBGXZWVOY-UHFFFAOYSA-N
Smiles Clc1ccc(cc1)C2OC2c3ccccc3
InChI
InChI=1S/C14H11ClO/c15-12-8-6-11(7-9-12)14-13(16-14)10-4-2-1-3-5-10/h1-9,13-14H

Physicochemical Descriptors

Property Name Value
Molecular Formula C14H11ClO
Molecular Weight 230.69
AlogP 3.76
Hydrogen Bond Acceptor 1.0
Hydrogen Bond Donor 0.0
Number of Rotational Bond 2.0
Polar Surface Area 12.53
Molecular species None
Aromatic Rings 2.0
Heavy Atoms 16.0
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 0.0 %
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 0.0 %
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 0.0 %
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 24.0 %
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 26.0 %
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 28.0 %

Cross References

Resources Reference
ChEMBL CHEMBL2251572
PubChem 608511
SureChEMBL SCHEMBL4388071