(E)-2-[2-(4-CHLORO-2-METHYLPHENOXYMETHYL)-ALPHA-METHOXYIMINOBENZYL]-1-METHYLIMIDAZOLE


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 ...


Active Pharmaceutical Ingredients Bioactive chemicals	Exact Similarity SubStructure	Threshold (%) >= 70

Structure


InChI Key	NECNLQYUBKYFLV-FCDQGJHFSA-N
Smiles	CO\N=C(/c1ccccc1COc2ccc(Cl)cc2C)\c3nccn3C
InChI	InChI=1S/C20H20ClN3O2/c1-14-12-16(21)8-9-18(14)26-13-15-6-4-5-7-17(15)19(23-25-3)20-22-10-11-24(20)2/h4-12H,13H2,1-3H3/b23-19+

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C20H20ClN3O2
Molecular Weight	369.84
AlogP	4.56
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	6.0
Polar Surface Area	48.64
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	26.0

Assay Description	Organism	Bioactivity
Curative fungicidal activity against Botryotinia fuckeliana infected cucumber plant at 7.8 ppm by foliar application	Botryotinia fuckeliana	55.0 %
Curative fungicidal activity against Botryotinia fuckeliana infected cucumber plant at 31.3 ppm by foliar application	Botryotinia fuckeliana	55.0 %
Preventive fungicidal activity against Botryotinia fuckeliana infected cucumber plant at 7.8 ppm by foliar application	Botryotinia fuckeliana	60.0 %
Preventive fungicidal activity against Botryotinia fuckeliana infected cucumber plant at 31.3 ppm by foliar application	Botryotinia fuckeliana	55.0 %
Curative fungicidal activity against Podosphaera fuliginea infected cucumber plant at 7.8 ppm by foliar application	Podosphaera fuliginea	100.0 %
Curative fungicidal activity against Podosphaera fuliginea infected cucumber plant at 31.3 ppm by foliar application	Podosphaera fuliginea	100.0 %
Preventive fungicidal activity against Podosphaera fuliginea infected cucumber plant at 7.8 ppm by foliar application	Podosphaera fuliginea	100.0 %
Preventive fungicidal activity against Podosphaera fuliginea infected cucumber plant at 31.3 ppm by foliar application	Podosphaera fuliginea	100.0 %
Fungicidal activity against Botryotinia fuckeliana infected cucumber plant at 7.8 ppm by foliar application	Botryotinia fuckeliana	90.0 %
Fungicidal activity against Podosphaera fuliginea infected cucumber plant at 7.8 ppm by foliar application	Podosphaera fuliginea	90.0 %
Antifungal activity against Botryotinia fuckeliana in cucumber at 7.8 ppm	Botryotinia fuckeliana	50.0 %
Antifungal activity against Podosphaera fuliginea in cucumber at 2 ppm	Podosphaera fuliginea	90.0 %
Antifungal activity against Pseudoperonospora cubensis in cucumber at 500 ppm	Pseudoperonospora cubensis	50.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2286158
PubChem	76330954

CONTENTS


PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).