(E)-METHYL 2-(2-((3-((E)-3-(2-CHLOROPHENYL)ACRYLOYL)PHENOXY)METHYL)PHENYL)-3-METHOXYACRYLATE


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	ZZONOFBXNDLVNY-VYJCLQOASA-N
Smiles	CO\C=C(\C(=O)OC)/c1ccccc1COc2cccc(c2)C(=O)\C=C\c3ccccc3Cl
InChI	InChI=1S/C27H23ClO5/c1-31-18-24(27(30)32-2)23-12-5-3-9-21(23)17-33-22-11-7-10-20(16-22)26(29)15-14-19-8-4-6-13-25(19)28/h3-16,18H,17H2,1-2H3/b15-14+,24-18+

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C27H23ClO5
Molecular Weight	462.92
AlogP	5.67
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	10.0
Polar Surface Area	61.83
Molecular species	None
Aromatic Rings	3.0
Heavy Atoms	33.0

Assay Description	Organism	Bioactivity
Antifungal activity against Pseudoperonospora cubensis in cucumber plants under greenhouse conditions assessed as fungicidal activity by in vivo assay	Pseudoperonospora cubensis	118.52 ug ml-1
Antifungal activity against Pseudoperonospora cubensis in cucumber plants under greenhouse conditions assessed as fungicidal activity at 25 mg/mL by in vivo assay	Pseudoperonospora cubensis	69.0 %
Antifungal activity against Pseudoperonospora cubensis in cucumber plants under greenhouse conditions assessed as fungicidal activity at 50 mg/mL by in vivo assay	Pseudoperonospora cubensis	77.0 %
Antifungal activity against Pseudoperonospora cubensis in cucumber plants under greenhouse conditions assessed as fungicidal activity at 100 mg/mL by in vivo assay	Pseudoperonospora cubensis	85.0 %
Antifungal activity against Podosphaera fuliginea in cucumber plants under greenhouse conditions assessed as fungicidal activity at 100 mg/mL by in vivo assay	Podosphaera fuliginea	22.0 %
Antifungal activity against Rhizoctonia solani assessed as fungicidal activity at 200 mg/L (beneficial crop - cucumber)	Rhizoctonia solani	0.0 %
Antifungal activity against Botryotinia fuckeliana assessed as fungicidal activity at 200 mg/L (beneficial crop - cucumber)	Botryotinia fuckeliana	0.0 %
Antifungal activity against Podosphaera fuliginea assessed as fungicidal activity at 200 mg/L (beneficial crop - cucumber)	Podosphaera fuliginea	94.0 %
Antifungal activity against Pseudoperonospora cubensis assessed as fungicidal activity at 200 mg/L (beneficial crop - cucumber)	Pseudoperonospora cubensis	98.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2251511

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).