(E/Z)-13-(2-(2,4-DICHLOROPHENOXY)ACETOXYIMINO)OXACYCLOHEXADECAN-2-ONE


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	WKKURTNVWLZEHM-UHFFFAOYSA-N
Smiles	Clc1ccc(OCC(=O)O\N=C\2/CCCCCCCCCCC(=O)OCCC2)c(Cl)c1
InChI	InChI=1S/C23H31Cl2NO5/c24-18-13-14-21(20(25)16-18)30-17-23(28)31-26-19-10-7-5-3-1-2-4-6-8-12-22(27)29-15-9-11-19/h13-14,16H,1-12,15,17H2

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C23H31Cl2NO5
Molecular Weight	472.4
AlogP	6.59
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	5.0
Polar Surface Area	74.19
Molecular species	None
Aromatic Rings	1.0
Heavy Atoms	31.0

Assay Description	Organism	Bioactivity
Herbicidal activity against Festuca arundinacea assessed as plant dead at 25 to 32 degC measured after 7 days	Festuca arundinacea	50.2 ug.mL-1
Herbicidal activity against Oryza sativa (rice) assessed as plant dead at 25 to 32 degC measured after 7 days	Oryza sativa	2.5 ug.mL-1
Herbicidal activity against Zea mays (maize) assessed as plant dead at 25 to 32 degC measured after 7 days	Zea mays	0.3 ug.mL-1
Herbicidal activity against Triticum aestivum L. (wheat) assessed as plant dead at 25 to 32 degC measured after 7 days	Triticum aestivum	38.4 ug.mL-1
Herbicidal activity against Glycine max (soybean) assessed as plant dead at 25 to 32 degC measured after 7 days	Glycine max	14.4 ug.mL-1
Herbicidal activity against Vigna radiata var. radiata assessed as plant dead at 25 to 32 degC measured after 7 days	Vigna radiata var. radiata	2.8 ug.mL-1
Herbicidal activity against Cucumis sativus (cucumber) assessed as plant dead at 25 to 32 degC measured after 7 days	Cucumis sativus	1.5 ug.mL-1
Herbicidal activity against Amaranthus tricolor assessed as plant dead at 25 to 32 degC measured after 7 days	Amaranthus tricolor	7.7 ug.mL-1

Cross References

Resources	Reference
ChEMBL	CHEMBL2229012
PubChem	74406870

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).