1-METHYL-N-(5-BROMOPYRIDIN-2-YL)-3-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXAMIDE


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	QRKGCLOTACZLCC-UHFFFAOYSA-N
Smiles	Cn1cc(C(=O)Nc2ccc(Br)cn2)c(n1)C(F)(F)F
InChI	InChI=1S/C11H8BrF3N4O/c1-19-5-7(9(18-19)11(13,14)15)10(20)17-8-3-2-6(12)4-16-8/h2-5H,1H3,(H,16,17,20)

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C11H8BrF3N4O
Molecular Weight	349.11
AlogP	2.77
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	3.0
Polar Surface Area	59.81
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	20.0

Assay Description	Organism	Bioactivity
Antifungal activity against Cytospora mandshurica assessed as inhibition of mycelium growth	Cytospora	132.5 ug.mL-1
Antifungal activity against Fusarium oxysporum assessed as inhibition of mycelium growth	Fusarium oxysporum	97.8 ug.mL-1
Antifungal activity against Fusarium oxysporum assessed as inhibition of mycelium growth at 100 ug/ml	Fusarium oxysporum	53.5 %
Antifungal activity against Cytospora mandshurica assessed as inhibition of mycelium growth at 100 ug/ml	Cytospora	48.7 %
Antifungal activity against Fusarium graminearum assessed as inhibition of mycelium growth	Fusarium graminearum	76.3 ug.mL-1
Antifungal activity against Fusarium graminearum assessed as inhibition of mycelium growth at 100 ug/ml	Fusarium graminearum	73.2 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2288636
PubChem	76327451

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).