2,2-DIBROMO-3,3-DIMETHYL-N-(5-(PERFLUOROBUTYL)-1,3,4-THIADIAZOL-2-YL)BUTANAMIDE


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	CSXCUOMWQLQRRE-UHFFFAOYSA-N
Smiles	CC(C)(C)C(Br)(Br)C(=O)Nc1nnc(s1)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
InChI	InChI=1S/C12H10Br2F9N3OS/c1-7(2,3)8(13,14)4(27)24-6-26-25-5(28-6)9(15,16)10(17,18)11(19,20)12(21,22)23/h1-3H3,(H,24,26,27)

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C12H10Br2F9N3OS
Molecular Weight	575.09
AlogP	5.3
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	7.0
Polar Surface Area	83.12
Molecular species	ACID
Aromatic Rings	1.0
Heavy Atoms	28.0

Assay Description	Organism	Bioactivity
Acaricidal activity against Tetranychus urticae (two-spotted spider mite) assessed as mite mortality at 3.13 ppm relative to untreated control	Tetranychus urticae	None
Acaricidal activity against Tetranychus urticae (two-spotted spider mite) assessed as mite mortality at 12.5 ppm relative to untreated control	Tetranychus urticae	30.0 %
Acaricidal activity against Tetranychus urticae (two-spotted spider mite) assessed as mite mortality at 50 ppm relative to untreated control	Tetranychus urticae	100.0 %
Acaricidal activity against Tetranychus urticae (two-spotted spider mite) assessed as mite mortality at 500 ppm relative to untreated control	Tetranychus urticae	100.0 %
Acaricidal activity against Tetranychus urticae (two-spotted spider mite) assessed as mite mortality at 200 ppm relative to untreated control	Tetranychus urticae	100.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2268671
PubChem	76334004

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).