Services
Research
Training
Industry
About us
ChEBI
Examples:
iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
Advanced
Home
Advanced Search
Browse
Documentation
Download
Tools
About ChEBI
Submit
Contact us
DiNA
Statistics
Entity of the Month
Periodic Table
Ontology
Train online
User Manual
Annotation Manual
Developer Manual
FAQ's
BiNChE
libChEBI
Web Services
ChEBI
> Main
CHEBI:39171 - nitenpyram
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
nitenpyram
ChEBI ID
CHEBI:39171
Definition
A
C
-nitro compound consisting of 2-nitroethene-1,1-diamine where one of the nitrogens bears ethyl and (6-chloro-3-pyridinyl)methyl while the other nitrogen carries a methyl group.
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download
Molfile
XML
SDF
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
Formula
C11H15ClN4O2
Net Charge
0
Average Mass
270.71500
Monoisotopic Mass
270.08835
InChI
InChI=1S/C11H15ClN4O2/c1-3-15(11(13-2)8-16(17)18)7-9-4-5-10(12)14-6-9/h4-6,8,13H,3,7H2,1-2H3
InChIKey
CFRPSFYHXJZSBI-UHFFFAOYSA-N
SMILES
[H]C(=C(NC)N(CC)Cc1ccc(Cl)nc1)[N+]([O-])=O
Roles Classification
Biological Role
(s):
neonicotinoid insectide
A class of neuro-active insecticides that act at the nicotinic acetylcholine receptor.
Application
(s):
neonicotinoid insectide
A class of neuro-active insecticides that act at the nicotinic acetylcholine receptor.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
nitenpyram (
CHEBI:39171
)
has functional parent
2-chloropyridine (
CHEBI:39174
)
nitenpyram (
CHEBI:39171
)
has role
neonicotinoid insectide (
CHEBI:25540
)
nitenpyram (
CHEBI:39171
)
is a
C
-nitro compound (
CHEBI:35716
)
nitenpyram (
CHEBI:39171
)
is a
monochloropyridine (
CHEBI:39172
)
Incoming
(
E
)-nitenpyram (
CHEBI:39170
)
is a
nitenpyram (
CHEBI:39171
)
IUPAC Name
N
-[(6-chloropyridin-3-yl)methyl]-
N
-ethyl-
N
'-methyl-2-nitroethene-1,1-diamine
Registry Numbers
Types
Sources
8553513
Beilstein Registry Number
Beilstein
8553513
Reaxys Registry Number
Reaxys
Citations
Types
Sources
10789501
PubMed citation
Europe PMC
21714058
PubMed citation
Europe PMC
Last Modified
12 February 2015