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 SLNCTQCXEXOORY-UHFFFAOYSA-N
Smiles CO\N=C/1\NCCN(Cc2ccc(Cl)nc2)C1=O
InChI
InChI=1S/C11H13ClN4O2/c1-18-15-10-11(17)16(5-4-13-10)7-8-2-3-9(12)14-6-8/h2-3,6H,4-5,7H2,1H3,(H,13,15)

Physicochemical Descriptors

Property Name Value
Molecular Formula C11H13ClN4O2
Molecular Weight 268.7
AlogP 0.17
Hydrogen Bond Acceptor 5.0
Hydrogen Bond Donor 1.0
Number of Rotational Bond 3.0
Polar Surface Area 66.82
Molecular species NEUTRAL
Aromatic Rings 1.0
Heavy Atoms 18.0
Assay Description Organism Bioactivity Reference
Insecticidal activity against Aphis gossypii (cotton aphid) infested expanded cotyledon stage of summer crookneck squash seedlings assessed as mortality at 50 ppm applied as spray after 72 hr by dissecting binocular microscopic analysis relative to control Aphis gossypii 90.0 %
Displacement of [3H]imidacloprid from nicotinic acetylcholine receptor in Musca domestica (house fly) head membrane after 1 hr by liquid scintillation counting analysis Musca domestica 1530.0 nM
Insecticidal activity against Aphis gossypii (cotton aphid) infested expanded cotyledon stage of summer crookneck squash seedlings assessed as mortality at 0.5 ppm applied as spray after 72 hr by dissecting binocular microscopic analysis relative to control Aphis gossypii 50.0 %
Insecticidal activity against Aphis gossypii (cotton aphid) infested expanded cotyledon stage of summer crookneck squash seedlings assessed as mortality at 5 ppm applied as spray after 72 hr by dissecting binocular microscopic analysis relative to control Aphis gossypii 70.0 %

Cross References

Resources Reference
ChEMBL CHEMBL2272694
PubChem 10869295