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:73450 - Asp-Gly
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
Asp-Gly
ChEBI ID
CHEBI:73450
Definition
A dipeptide composed of
L
-aspartic acid and glycine joined by a peptide linkage.
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
C6H10N2O5
Net Charge
0
Average Mass
190.15400
Monoisotopic Mass
190.05897
InChI
InChI=1S/C6H10N2O5/c7-3(1-4(9)10)6(13)8-2-5(11)12/h3H,1-2,7H2,(H,8,13)(H,9,10)(H,11,12)/t3-/m0/s1
InChIKey
JHFNSBBHKSZXKB-VKHMYHEASA-N
SMILES
N[C@@H](CC(O)=O)C(=O)NCC(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
)
Biological Role
(s):
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
Asp-Gly (
CHEBI:73450
)
has functional parent
L
-aspartic acid (
CHEBI:17053
)
Asp-Gly (
CHEBI:73450
)
has functional parent
glycine (
CHEBI:15428
)
Asp-Gly (
CHEBI:73450
)
has role
metabolite (
CHEBI:25212
)
Asp-Gly (
CHEBI:73450
)
is a
dipeptide (
CHEBI:46761
)
Asp-Gly (
CHEBI:73450
)
is conjugate acid of
Asp-Gly(1−) (
CHEBI:191203
)
Incoming
Asp-Gly(1−) (
CHEBI:191203
)
is conjugate base of
Asp-Gly (
CHEBI:73450
)
IUPAC Name
L
-α-aspartylglycine
Synonyms
Sources
D-G
ChEBI
DG
ChEBI
L
-Asp-Gly
ChEBI
Manual Xref
Database
HMDB0028753
HMDB
View more database links
Registry Number
Type
Source
3790-51-0
CAS Registry Number
ChemIDplus
Citation
Type
Source
16584231
PubMed citation
Europe PMC
Last Modified
25 April 2022