2-(METHYLSULFONYL)-5-(2,6-DIFLUOROPHENYL)-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	XLQQPFQTFGSMFH-UHFFFAOYSA-N
Smiles	CS(=O)(=O)c1oc(nn1)c2c(F)cccc2F
InChI	InChI=1S/C9H6F2N2O3S/c1-17(14,15)9-13-12-8(16-9)7-5(10)3-2-4-6(7)11/h2-4H,1H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C9H6F2N2O3S
Molecular Weight	260.22
AlogP	1.61
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	2.0
Polar Surface Area	81.44
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	17.0

Assay Description	Organism	Bioactivity
Antifungal activity against Cytospora mandshurica assessed as mycelial growth inhibition	Cytospora	38.27 ug.mL-1
Antifungal activity against Fusarium oxysporum assessed as mycelial growth inhibition	Fusarium oxysporum	65.75 ug.mL-1
Antifungal activity against Thanatephorus cucumeris assessed as mycelial growth inhibition	Thanatephorus cucumeris	23.35 ug.mL-1
Antifungal activity against Sclerotinia sclerotiorum assessed as mycelial growth inhibition	Sclerotinia sclerotiorum	14.97 ug.mL-1
Antifungal activity against Colletotrichum gloeosporioides assessed as mycelial growth inhibition	Colletotrichum gloeosporioides	26.07 ug.mL-1
Antifungal activity against Phytophthora infestans assessed as mycelial growth inhibition	Phytophthora infestans	59.52 ug.mL-1
Antifungal activity against Botryotinia fuckeliana assessed as mycelial growth inhibition	Botryotinia fuckeliana	8.25 ug.mL-1
Antifungal activity against Rhizoctonia solani assessed as mycelial growth inhibition	Rhizoctonia solani	21.23 ug.mL-1
Antifungal activity against Cytospora mandshurica at 50 ug/ml after 5 days by poison plate technique	Cytospora	97.8 %
Antifungal activity against Fusarium oxysporum at 50 ug/ml after 5 days by poison plate technique	Fusarium oxysporum	98.8 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2252858
PubChem	76308303

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).