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:132225 -
D
-homocysteic acid
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
D
-homocysteic acid
ChEBI ID
CHEBI:132225
ChEBI ASCII Name
D-homocysteic acid
Definition
A homocysteic acid with
D
-configuration.
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
C4H9NO5S
Net Charge
0
Average Mass
183.184
Monoisotopic Mass
183.02014
InChI
InChI=1S/C4H9NO5S/c5-3(4(6)7)1-2-11(8,9)10/h3H,1-2,5H2,(H,6,7)(H,8,9,10)/t3-/m1/s1
InChIKey
VBOQYPQEPHKASR-GSVOUGTGSA-N
SMILES
OC([C@@H](CCS(O)(=O)=O)N)=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):
metabotropic glutamate receptor agonist
An agonist that selectively binds to and activates a metabotropic glutamate receptor.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-homocysteic acid (
CHEBI:132225
)
has role
metabotropic glutamate receptor agonist (
CHEBI:61966
)
D
-homocysteic acid (
CHEBI:132225
)
is a
homocysteic acid (
CHEBI:90324
)
D
-homocysteic acid (
CHEBI:132225
)
is enantiomer of
L
-homocysteic acid (
CHEBI:132223
)
Incoming
D
L
-homocysteic acid (
CHEBI:132221
)
has part
D
-homocysteic acid (
CHEBI:132225
)
L
-homocysteic acid (
CHEBI:132223
)
is enantiomer of
D
-homocysteic acid (
CHEBI:132225
)
IUPAC Name
(2
R
)-2-amino-4-sulfobutanoic acid
Synonyms
Sources
(2
R
)-2-amino-4-sulfobutyric acid
ChEBI
(
R
)-2-amino-4-sulfobutanoic acid
ChEBI
(
R
)-2-amino-4-sulfobutyric acid
ChEBI
Registry Numbers
Types
Sources
56892-03-6
CAS Registry Number
ChemIDplus
6582338
Reaxys Registry Number
Reaxys
Citations
Types
Sources
10209293
PubMed citation
Europe PMC
1279472
PubMed citation
Europe PMC
19906886
PubMed citation
Europe PMC
Last Modified
17 June 2016