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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:132223 -
L
-homocysteic acid
Main
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ChEBI Name
L
-homocysteic acid
ChEBI ID
CHEBI:132223
ChEBI ASCII Name
L-homocysteic acid
Definition
A homocysteic acid with
L
-configuration.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:80543
Supplier Information
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Wikipedia
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Read full article at Wikipedia
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-/m0/s1
InChIKey
VBOQYPQEPHKASR-VKHMYHEASA-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):
NMDA receptor agonist
An excitatory amino acid agonist which binds to NMDA receptors and triggers a response.
Application
(s):
NMDA receptor agonist
An excitatory amino acid agonist which binds to NMDA receptors and triggers a response.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
L
-homocysteic acid (
CHEBI:132223
)
has role
NMDA receptor agonist (
CHEBI:64571
)
L
-homocysteic acid (
CHEBI:132223
)
is a
homocysteic acid (
CHEBI:90324
)
L
-homocysteic acid (
CHEBI:132223
)
is enantiomer of
D
-homocysteic acid (
CHEBI:132225
)
Incoming
D
L
-homocysteic acid (
CHEBI:132221
)
has part
L
-homocysteic acid (
CHEBI:132223
)
D
-homocysteic acid (
CHEBI:132225
)
is enantiomer of
L
-homocysteic acid (
CHEBI:132223
)
IUPAC Name
(2
S
)-2-amino-4-sulfobutanoic acid
Synonyms
Sources
(2
S
)-2-amino-4-sulfobutyric acid
ChEBI
(
S
)-2-amino-4-sulfobutanoic acid
ChEBI
(
S
)-2-amino-4-sulfobutyric acid
ChEBI
homocysteic acid
ChEBI
L-2-amino-4-sulfobutyric acid
HMDB
Manual Xrefs
Databases
C16511
KEGG COMPOUND
HMDB0002205
HMDB
Homocysteic_acid
Wikipedia
View more database links
Registry Numbers
Types
Sources
14857-77-3
CAS Registry Number
KEGG COMPOUND
14857-77-3
CAS Registry Number
ChemIDplus
5735822
Reaxys Registry Number
Reaxys
Citations
Types
Sources
25592718
PubMed citation
Europe PMC
27046337
PubMed citation
Europe PMC
Last Modified
17 June 2016