N-(1-(4-CHLORO-2-METHOXYPHENYL)ETHYL)-2-CYANO-3,3-DIMETHYLPENT-4-ENAMIDE


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	HOOXADQKKTZKLI-UHFFFAOYSA-N
Smiles	COc1cc(Cl)ccc1C(C)NC(=O)C(C#N)C(C)(C)C=C
InChI	InChI=1S/C17H21ClN2O2/c1-6-17(3,4)14(10-19)16(21)20-11(2)13-8-7-12(18)9-15(13)22-5/h6-9,11,14H,1H2,2-5H3,(H,20,21)

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C17H21ClN2O2
Molecular Weight	320.81
AlogP	3.48
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	6.0
Polar Surface Area	62.12
Molecular species	NEUTRAL
Aromatic Rings	1.0
Heavy Atoms	22.0

Assay Description	Organism	Bioactivity	Reference
Fungicidal activity against Magnaporthe grisea in rice plant assessed as prevention from rice blast disease measured as lesions under greenhouse at 50 ppm for 8 days by soil drench compound treated before inoculation	Magnaporthe grisea	10.0 %
Fungicidal activity against Magnaporthe grisea in rice plant assessed as prevention from rice blast disease measured as lesions under greenhouse at 3.1 ppm for 8 days by foliar spray compound treated before inoculation	Magnaporthe grisea	10.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2286888
PubChem	15135410
SureChEMBL	SCHEMBL9760103

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).