(R,R)(+)-2-(4-(5-CHLORO-3-FLUOROPYRIDIN-2-YLOXY)PHENOXY)PROPIONIC ACID 4-(1-ETHOXYCARBONYL-ETHOXY)-PHENYL ESTER


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	IWNZCKQEOQZUEL-HZPDHXFCSA-N
Smiles	CCOC(=O)[C@@H](C)Oc1ccc(OC(=O)[C@@H](C)Oc2ccc(Oc3ncc(Cl)cc3F)cc2)cc1
InChI	InChI=1S/C25H23ClFNO7/c1-4-31-24(29)15(2)32-18-7-11-21(12-8-18)35-25(30)16(3)33-19-5-9-20(10-6-19)34-23-22(27)13-17(26)14-28-23/h5-16H,4H2,1-3H3/t15-,16-/m1/s1

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C25H23ClFNO7
Molecular Weight	503.9
AlogP	5.92
Hydrogen Bond Acceptor	8.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	12.0
Polar Surface Area	93.18
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	35.0

Assay Description	Organism	Bioactivity
Herbicidal activity against Avena fatua assessed as growth inhibition at 125 g/ha after 3 weeks relative to control	Avena fatua	93.0 %
Herbicidal activity against Alopecurus myosuroides assessed as growth inhibition at 125 g/ha after 3 weeks relative to control	Alopecurus myosuroides	90.0 %
Herbicidal activity against Echinochloa crus-galli (barnyard grass) assessed as growth inhibition at 125 g/ha after 3 weeks relative to control	Echinochloa crus-galli	80.0 %
Phytotoxicity against Triticum aestivum (wheat) assessed as growth inhibition at 125 g/ha after 3 weeks relative to control	Triticum aestivum	0.0 %
Phytoxicity against Hordeum vulgare (barley) assessed as growth inhibition at 125 g/ha after 3 weeks relative to control	Hordeum vulgare	10.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2286490
PubChem	76316395

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).