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:64305 - 2-aminopimelic acid
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
2-aminopimelic acid
ChEBI ID
CHEBI:64305
Definition
An amino dicarboxylic acid that is heptanedioic acid in which a hydrogen at position 2 is replaced by an amino group. It is a component of the cell wall peptidoglycan of bacteria.
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
C7H13NO4
Net Charge
0
Average Mass
175.18240
Monoisotopic Mass
175.08446
InChI
InChI=1S/C7H13NO4/c8-5(7(11)12)3-1-2-4-6(9)10/h5H,1-4,8H2,(H,9,10)(H,11,12)
InChIKey
JUQLUIFNNFIIKC-UHFFFAOYSA-N
SMILES
NC(CCCCC(O)=O)C(O)=O
Roles Classification
Chemical Role
(s):
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
Biological Role
(s):
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
2-aminopimelic acid (
CHEBI:64305
)
has role
bacterial metabolite (
CHEBI:76969
)
2-aminopimelic acid (
CHEBI:64305
)
is a
amino dicarboxylic acid (
CHEBI:36164
)
2-aminopimelic acid (
CHEBI:64305
)
is a
non-proteinogenic α-amino acid (
CHEBI:83925
)
Incoming
L
-2-aminopimelic acid (
CHEBI:44387
)
is a
2-aminopimelic acid (
CHEBI:64305
)
IUPAC Name
2-aminoheptanedioic acid
Synonyms
Sources
α-aminopimelic acid
ChemIDplus
Apm
ChEBI
Manual Xref
Database
HMDB0034252
HMDB
View more database links
Registry Numbers
Types
Sources
1724722
Reaxys Registry Number
Reaxys
3721-85-5
CAS Registry Number
ChemIDplus
Citations
Types
Sources
2019472
PubMed citation
Europe PMC
3079832
PubMed citation
Europe PMC
Last Modified
26 March 2015