N-ETHYL-N-METHYL-2-NITRO-N-((TETRAHYDROFURAN-3-YL)METHYL)ETHENE-1,1-DIAMINE


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	PUSVVOZJZNYOPO-JXMROGBWSA-N
Smiles	CCN(CC1CCOC1)\C(=C\[N+](=O)[O-])\NC
InChI	InChI=1S/C10H19N3O3/c1-3-12(6-9-4-5-16-8-9)10(11-2)7-13(14)15/h7,9,11H,3-6,8H2,1-2H3/b10-7+

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C10H19N3O3
Molecular Weight	229.28
AlogP	0.36
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	6.0
Polar Surface Area	70.31
Molecular species	NEUTRAL
Aromatic Rings	0.0
Heavy Atoms	16.0

Assay Description	Organism	Bioactivity
Binding affinity to Nephotettix cincticeps (green rice leafhopper) nicotinic acetylcholine receptor	Nephotettix cincticeps	None
Binding affinity to Laodelphax striatella (small brown planthopper) nicotinic acetylcholine receptor	Laodelphax striatella	None
Insecticidal activity against Nephotettix cincticeps (green rice leafhopper) assessed as lethality at 1 to 10 ppm	Nephotettix cincticeps	70.0 %
Insecticidal activity against Laodelphax striatella (small brown planthopper) assessed as lethality at 10 to 100 ppm	Laodelphax striatella	70.0 %
Insecticidal activity against 1 to 3 day-old adult Nephotettix cincticeps (green rice leafhopper) infested in compound-treated rice seedlings assessed as mortality measured after 3 days	Nephotettix cincticeps	10.0 ppm
Insecticidal activity against 1 to 3 day-old adult Laodelphax striatella (small brown planthopper) infested compound-treated rice seedlings assessed as mortality measured after 3 days	Laodelphax striatella	1.0 ppm

Cross References

Resources	Reference
ChEMBL	CHEMBL2229763
PubChem	15278161
SureChEMBL	SCHEMBL8550998

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).