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:133665 -
N
-(2-furoyl)glycinate
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
N
-(2-furoyl)glycinate
ChEBI ID
CHEBI:133665
ChEBI ASCII Name
N-(2-furoyl)glycinate
Definition
A monocarboxylic acid anion that is the conjugate base of
N
-(2-furoyl)glycine, obtained by deprotonation of the carboxy group; major species at pH 7.3.
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
C7H6NO4
Net Charge
-1
Average Mass
168.127
Monoisotopic Mass
168.03023
InChI
InChI=1S/C7H7NO4/c9-6(10)4-8-7(11)5-2-1-3-12-5/h1-3H,4H2,(H,8,11)(H,9,10)/p-1
InChIKey
KSPQDMRTZZYQLM-UHFFFAOYSA-M
SMILES
O1C=CC=C1C(NCC([O-])=O)=O
Roles Classification
Biological Role
(s):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
N
-(2-furoyl)glycinate (
CHEBI:133665
)
has role
human metabolite (
CHEBI:77746
)
N
-(2-furoyl)glycinate (
CHEBI:133665
)
is a
N
-acylglycinate (
CHEBI:57670
)
N
-(2-furoyl)glycinate (
CHEBI:133665
)
is a
monocarboxylic acid anion (
CHEBI:35757
)
N
-(2-furoyl)glycinate (
CHEBI:133665
)
is conjugate base of
N
-(2-furoyl)glycine (
CHEBI:82912
)
Incoming
N
-(2-furoyl)glycine (
CHEBI:82912
)
is conjugate acid of
N
-(2-furoyl)glycinate (
CHEBI:133665
)
IUPAC Name
[(furan-2-carbonyl)amino]acetate
Synonyms
Sources
furoylglycinate
ChEBI
N
-(furan-2-ylcarbonyl)glycinate
ChEBI
pyromucurate
ChEBI
Registry Number
Type
Source
5657-19-2
CAS Registry Number
ChemIDplus
Last Modified
13 October 2016