2-(DIETHYLAMINO)-6-METHYLPYRIMIDIN-4-YL DIMETHYLCARBAMATE


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	OPYWWMLAMDZTER-UHFFFAOYSA-N
Smiles	CCN(CC)c1nc(C)cc(OC(=O)N(C)C)n1
InChI	InChI=1S/C12H20N4O2/c1-6-16(7-2)11-13-9(3)8-10(14-11)18-12(17)15(4)5/h8H,6-7H2,1-5H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C12H20N4O2
Molecular Weight	252.31
AlogP	2.22
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	5.0
Polar Surface Area	58.56
Molecular species	NEUTRAL
Aromatic Rings	1.0
Heavy Atoms	18.0

Assay Description	Organism	Bioactivity
Potentiation of pirimiphos-methyl-induced insecticidal activity against OP-resistant Chilo suppressalis Hata-f (rice stem borer) assessed as synergistic ratio at 1:10 pirimiphos-methyl to compound ratio relative to pirimiphos-methyl alone	Chilo suppressalis	451.0
Potentiation of fenitrothion-induced insecticidal activity against OP-susceptible Chilo suppressalis (rice stem borer) S strain assessed as synergistic ratio at 1:10 fenitrothion to compound ratio relative to fenitrothion alone	Chilo suppressalis	1.0
Potentiation of pirimiphos-methyl-induced insecticidal activity against OP-resistant Chilo suppressalis Hata-f (rice stem borer) assessed as synergistic ratio at 1:5 pirimiphos-methyl to compound ratio relative to pirimiphos-methyl alone	Chilo suppressalis	440.0
Potentiation of pirimiphos-methyl-induced insecticidal activity against OP-resistant Chilo suppressalis Hata-f (rice stem borer) assessed as synergistic ratio at 1:1 pirimiphos-methyl to compound ratio relative to pirimiphos-methyl alone	Chilo suppressalis	86.0
Potentiation of fenitrothion-induced insecticidal activity against OP-resistant Chilo suppressalis Hata-f (rice stem borer) assessed as synergistic ratio at 1:10 fenitrothion to compound ratio relative to fenitrothion alone	Chilo suppressalis	20.0

Cross References

Resources	Reference
ChEMBL	CHEMBL2288462
PubChem	54163373
SureChEMBL	SCHEMBL988810

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).