5-((2-(((1-(4-BROMOPHENYL)ETHYLIDENE)HYDRAZONO)METHYL)PHENYL)(METHOXY)METHYL)-3-METHYLISOXAZOLE


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	JIXRDPZLPDASNQ-CLKIXKSOSA-N
Smiles	COC(c1onc(C)c1)c2ccccc2\C=N\N=C(/C)\c3ccc(Br)cc3
InChI	InChI=1S/C21H20BrN3O2/c1-14-12-20(27-25-14)21(26-3)19-7-5-4-6-17(19)13-23-24-15(2)16-8-10-18(22)11-9-16/h4-13,21H,1-3H3/b23-13+,24-15+

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C21H20BrN3O2
Molecular Weight	426.31
AlogP	4.56
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	6.0
Polar Surface Area	59.98
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	27.0

Assay Description	Organism	Bioactivity
Curative fungicidal activity against Pseudoperonospora cubensis infected cucumber leaves at 7.8 ppm after by foliar application method	Pseudoperonospora cubensis	100.0 %
Curative fungicidal activity against Pseudoperonospora cubensis infected cucumber leaves at 31.3 ppm after by foliar application method	Pseudoperonospora cubensis	100.0 %
Preventive fungicidal activity against Pseudoperonospora cubensis infected cucumber leaves at 31.3 ppm after by foliar application method	Pseudoperonospora cubensis	70.0 %
Preventive fungicidal activity against Pseudoperonospora cubensis infected cucumber leaves at 7.8 ppm after by foliar application method	Pseudoperonospora cubensis	50.0 %
Curative fungicidal activity against Podosphaera fuliginea infected cucumber leaves at 31.3 ppm after by foliar application method	Podosphaera fuliginea	70.0 %
Curative fungicidal activity against Podosphaera fuliginea infected cucumber leaves at 7.8 ppm after by foliar application method	Podosphaera fuliginea	50.0 %
Preventive fungicidal activity against Podosphaera fuliginea infected cucumber leaves at 31.3 ppm after by foliar application method	Podosphaera fuliginea	100.0 %
Preventive fungicidal activity against Podosphaera fuliginea infected cucumber leaves at 7.8 ppm after by foliar application method	Podosphaera fuliginea	100.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2289391
PubChem	76313077

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).