2-(4-METHOXYPHENYL)-5-(5-(4-NITROPHENYL)FURAN-2-YL)-1,3,4-OXADIAZOLE


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	CWRHEDMEGRIEHR-UHFFFAOYSA-N
Smiles	COc1ccc(cc1)c2oc(nn2)c3oc(cc3)c4ccc(cc4)[N+](=O)[O-]
InChI	InChI=1S/C19H13N3O5/c1-25-15-8-4-13(5-9-15)18-20-21-19(27-18)17-11-10-16(26-17)12-2-6-14(7-3-12)22(23)24/h2-11H,1H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C19H13N3O5
Molecular Weight	363.32
AlogP	4.14
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	5.0
Polar Surface Area	107.1
Molecular species	NEUTRAL
Aromatic Rings	4.0
Heavy Atoms	27.0

Assay Description	Organism	Bioactivity
Fungicidal activity against Rhizoctonia solani infected drug-pretreated cucumber two seeded leaves assessed as decrease in disease index at 500 ug/ml (acetone Rvb = 2.22 +/-0.79%)	Rhizoctonia solani	-3.97 %
Fungicidal activity against Botryotinia fuckeliana infected in drug-pretreated cucumber two seeded leaves assessed as decrease in disease index at 500 ug/ml (acetone Rvb = 1.53 +/-0.21%)	Botryotinia fuckeliana	47.83 %
Fungicidal activity against Corynespora cassiicola infected in drug-pretreated cucumber two seeded leaves assessed as decrease in disease index at 500 ug/ml (acetone Rvb = 5.23 +/-0.88%)	Corynespora cassiicola	10.59 %
Fungicidal activity against Cladosporium cucumerinum infected drug-pretreated cucumber two seeded leaves assessed as decrease in disease index at 500 ug/ml (acetone Rvb = 3.18 +/-0.75%)	Cladosporium cucumerinum	12.35 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2230284
PubChem	71517432

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).