3-(2,6-DIMETHYLBENZENESELENONYL)-[1,2,4]TRIAZOLE-1-CARBOXYLICACID DIETHYLAMIDE


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	RHJJOADQEXLVDJ-UHFFFAOYSA-N
Smiles	CCN(CC)C(=O)n1cnc(n1)[Se](=O)(=O)c2c(C)cccc2C
InChI	InChI=1S/C15H20N4O3Se/c1-5-18(6-2)15(20)19-10-16-14(17-19)23(21,22)13-11(3)8-7-9-12(13)4/h7-10H,5-6H2,1-4H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C15H20N4O3Se
Molecular Weight	383.3
AlogP	None
Hydrogen Bond Acceptor	None
Hydrogen Bond Donor	None
Number of Rotational Bond	None
Polar Surface Area	None
Molecular species	None
Aromatic Rings	None
Heavy Atoms	None

Assay Description	Organism	Bioactivity
Herbicidal activity against semen euphorbiae assessed as inhibition of weed growth at at 7.5 ug/mL measured 15 days post compound treatment by pot-culture method	Echinochloa crus-galli	88.9 %
Toxicity against Oryza sativa xiuanyou 63 (rice) assessed as growth inhibition at 7.5 ug/mL measured 15 days post compound treatment by pot-culture method	Oryza sativa	2.8 %
Herbicidal activity against Cucumis sativus jinyou 15 (cucumber) assessed as inhibition of weed growth at 3.75 ug/mL measured 15 days post compound treatment by pot-culture method	Cucumis sativus	100.0 %
Herbicidal activity against semen euphorbiae assessed as inhibition of weed growth at 500 ug/mL measured 15 days post compound treatment by pot-culture method	Echinochloa crus-galli	100.0 %
Herbicidal activity against Cucumis sativus jinyou 15 (cucumber) assessed as inhibition of weed growth at 500 ug/mL measured 15 days post compound treatment by pot-culture method	Cucumis sativus	100.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2253138
PubChem	16085815

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).