N-(4-CHLORO-2-(TRIFLUOROMETHYL)PHENYL)-2-OXOCYCLOHEPTANE-1-SULFONAMIDE


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	HHXYXPARZDOJIF-UHFFFAOYSA-N
Smiles	FC(F)(F)c1cc(Cl)ccc1NS(=O)(=O)C2CCCCCC2=O
InChI	InChI=1S/C14H15ClF3NO3S/c15-9-6-7-11(10(8-9)14(16,17)18)19-23(21,22)13-5-3-1-2-4-12(13)20/h6-8,13,19H,1-5H2

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C14H15ClF3NO3S
Molecular Weight	369.79
AlogP	3.69
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	4.0
Polar Surface Area	71.62
Molecular species	ACID
Aromatic Rings	1.0
Heavy Atoms	23.0

Assay Description	Organism	Bioactivity
Fungicidal activity against Botryotinia fuckeliana grown on compound pre-treated cucumber leaves assessed as control efficiency against gray mold disease on leaves at 31.25 ug/mL	Botryotinia fuckeliana	11.97 %
Fungicidal activity against Botryotinia fuckeliana grown on compound pre-treated cucumber leaves assessed as control efficiency against gray mold disease on leaves at 125 ug/mL	Botryotinia fuckeliana	21.95 %
Fungicidal activity against Botryotinia fuckeliana grown on compound pre-treated cucumber leaves assessed as control efficiency against gray mold disease on leaves at 500 ug/mL	Botryotinia fuckeliana	49.53 %
Fungicidal activity against Botryotinia fuckeliana assessed as inhibition spore germination	Botryotinia fuckeliana	387.82 ug ml-1	Fungicidal activity against Botryotinia fuckeliana assessed as inhibition spore germination	Botryotinia fuckeliana	18.07 ug.mL-1
Fungicidal activity against Botryotinia fuckeliana assessed as inhibition of mycelial growth	Botryotinia fuckeliana	3.7 ug ml-1	Fungicidal activity against Botryotinia fuckeliana assessed as inhibition of mycelial growth	Botryotinia fuckeliana	0.8 ug.mL-1

Cross References

Resources	Reference
ChEMBL	CHEMBL2229800
PubChem	49803778

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).