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 TXAWBKBMGZKBNN-UHFFFAOYSA-N
Smiles CCC(O)c1ccc(Cl)cc1
InChI
InChI=1S/C9H11ClO/c1-2-9(11)7-3-5-8(10)6-4-7/h3-6,9,11H,2H2,1H3

Physicochemical Descriptors

Property Name Value
Molecular Formula C9H11ClO
Molecular Weight 170.64
AlogP 2.79
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 11.0
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 28.0 %
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 41.0 %
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 51.0 %
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 61.0 %
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 77.0 %
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 95.0 %

Cross References

Resources Reference
ChEMBL CHEMBL2251579
PubChem 83774
SureChEMBL SCHEMBL868462