(Z)-2-ETHOXYETHYL 3-((6-CHLOROPYRIDIN-3-YL)METHYLAMINO)-2-CYANOPENT-2-ENOATE

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Search structure


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	GESZBOUFAGKSNF-YPKPFQOOSA-N
Smiles	CCOCCOC(=O)\C(=C(\CC)/NCc1ccc(Cl)nc1)\C#N
InChI	InChI=1S/C16H20ClN3O3/c1-3-14(19-10-12-5-6-15(17)20-11-12)13(9-18)16(21)23-8-7-22-4-2/h5-6,11,19H,3-4,7-8,10H2,1-2H3/b14-13-

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C16H20ClN3O3
Molecular Weight	337.8
AlogP	2.04
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	10.0
Polar Surface Area	84.24
Molecular species	NEUTRAL
Aromatic Rings	1.0
Heavy Atoms	23.0

Assay Description	Organism	Bioactivity	Reference
Phytotoxicity against Zea mays (maize) at 750 g/ha	Zea mays	None
Post-emergence herbicidal activity against Brassica napus (oilseed rape) at 75 g/ha applied through spraying after first true leaf expanded	Brassica napus	94.1 %
Post-emergence herbicidal activity against Brassica napus (oilseed rape) at 300 g/ha applied through spraying after first true leaf expanded	Brassica napus	98.4 %
Post-emergence herbicidal activity against Brassica napus (oilseed rape) at 1500 g/ha applied through spraying after first true leaf expanded	Brassica napus	100.0 %
Post-emergence herbicidal activity against Amaranthus retroflexus at 75 g/ha applied through spraying after first true leaf expanded	Amaranthus retroflexus	88.4 %
Post-emergence herbicidal activity against Amaranthus retroflexus at 300 g/ha applied through spraying after first true leaf expanded	Amaranthus retroflexus	100.0 %
Post-emergence herbicidal activity against Amaranthus retroflexus at 1500 g/ha applied through spraying after first true leaf expanded	Amaranthus retroflexus	100.0 %
Post-emergence herbicidal activity against Medicago sativa (alfalfa) at 75 g/ha applied through spraying after first true leaf expanded	Medicago sativa	45.3 %
Post-emergence herbicidal activity against Medicago sativa (alfalfa) at 300 g/ha applied through spraying after first true leaf expanded	Medicago sativa	62.8 %
Post-emergence herbicidal activity against Medicago sativa (alfalfa) at 1500 g/ha applied through spraying after first true leaf expanded	Medicago sativa	83.7 %
Pre-emergence herbicidal activity against Brassica napus (oilseed rape) at 1.5 kg/ha applied through spraying immediately after seed plantings	Brassica napus	75.0 %
Pre-emergence herbicidal activity against Amaranthus retroflexus at 1.5 kg/ha applied through spraying immediately after seed plantings	Amaranthus retroflexus	71.4 %
Pre-emergence herbicidal activity against Medicago sativa (alfalfa) at 1.5 kg/ha applied through spraying immediately after seed plantings	Medicago sativa	71.4 %
Post-emergence herbicidal activity against Brassica napus (oilseed rape) at 1.5 kg/ha applied through spraying after first true leaf expanded	Brassica napus	100.0 %
Post-emergence herbicidal activity against Amaranthus retroflexus at 1.5 kg/ha applied through spraying after first true leaf expanded	Amaranthus retroflexus	100.0 %
Post-emergence herbicidal activity against Medicago sativa (alfalfa) at 1.5 kg/ha applied through spraying after first true leaf expanded	Medicago sativa	83.7 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2273004
PubChem	11035122

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).