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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:16523 -
D
-serine
Main
ChEBI Ontology
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ChEBI Name
D
-serine
ChEBI ID
CHEBI:16523
ChEBI ASCII Name
D-serine
Definition
The
R
-enantiomer of serine.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:42262, CHEBI:143888, CHEBI:4245, CHEBI:13019, CHEBI:21090
Supplier Information
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Molfile
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Formula
C3H7NO3
Net Charge
0
Average Mass
105.09262
Monoisotopic Mass
105.04259
InChI
InChI=1S/C3H7NO3/c4-2(1-5)3(6)7/h2,5H,1,4H2,(H,6,7)/t2-/m1/s1
InChIKey
MTCFGRXMJLQNBG-UWTATZPHSA-N
SMILES
N[C@H](CO)C(O)=O
Metabolite of Species
Details
Escherichia coli
(NCBI:txid562)
See:
PubMed
Homo sapiens
(NCBI:txid9606)
See:
DOI
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):
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in
Escherichia coli
.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
NMDA receptor agonist
An excitatory amino acid agonist which binds to NMDA receptors and triggers a response.
fundamental metabolite
Any metabolite produced by all living cells.
(via
serine
)
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
D
-serine (
CHEBI:16523
)
has role
Escherichia coli
metabolite (
CHEBI:76971
)
D
-serine (
CHEBI:16523
)
has role
human metabolite (
CHEBI:77746
)
D
-serine (
CHEBI:16523
)
has role
NMDA receptor agonist (
CHEBI:64571
)
D
-serine (
CHEBI:16523
)
is a
D
-α-amino acid (
CHEBI:16733
)
D
-serine (
CHEBI:16523
)
is a
serine (
CHEBI:17822
)
D
-serine (
CHEBI:16523
)
is conjugate acid of
D
-serinate (
CHEBI:32840
)
D
-serine (
CHEBI:16523
)
is conjugate base of
D
-serinium (
CHEBI:32841
)
D
-serine (
CHEBI:16523
)
is enantiomer of
L
-serine (
CHEBI:17115
)
D
-serine (
CHEBI:16523
)
is tautomer of
D
-serine zwitterion (
CHEBI:35247
)
Incoming
D
-serine derivative (
CHEBI:84133
)
has functional parent
D
-serine (
CHEBI:16523
)
D
-serinium (
CHEBI:32841
)
is conjugate acid of
D
-serine (
CHEBI:16523
)
D
-serinate (
CHEBI:32840
)
is conjugate base of
D
-serine (
CHEBI:16523
)
L
-serine (
CHEBI:17115
)
is enantiomer of
D
-serine (
CHEBI:16523
)
D
-serine residue (
CHEBI:29998
)
is substituent group from
D
-serine (
CHEBI:16523
)
D
-serino group (
CHEBI:32843
)
is substituent group from
D
-serine (
CHEBI:16523
)
D
-seryl group (
CHEBI:32842
)
is substituent group from
D
-serine (
CHEBI:16523
)
D
-serine zwitterion (
CHEBI:35247
)
is tautomer of
D
-serine (
CHEBI:16523
)
IUPAC Name
D
-serine
Synonyms
Sources
(2
R
)-2-amino-3-hydroxypropanoic acid
IUPAC
(R)-2-Amino-3-hydroxy-propionic acid
ChEMBL
(
R
)-2-amino-3-hydroxypropanoic acid
ChEBI
D
-Serin
ChEBI
D-Serine
KEGG COMPOUND
D-SERINE
PDBeChem
DSN
PDBeChem
Manual Xrefs
Databases
C00740
KEGG COMPOUND
D-SERINE
MetaCyc
DB03929
DrugBank
DSN
PDBeChem
ECMDB03406
ECMDB
HMDB0003406
HMDB
YMDB00284
YMDB
View more database links
Registry Numbers
Types
Sources
1041392
Gmelin Registry Number
Gmelin
1721403
Beilstein Registry Number
Beilstein
1721403
Reaxys Registry Number
Reaxys
312-84-5
CAS Registry Number
KEGG COMPOUND
312-84-5
CAS Registry Number
NIST Chemistry WebBook
312-84-5
CAS Registry Number
ChemIDplus
Citations
Types
Sources
11864625
PubMed citation
Europe PMC
12850593
PubMed citation
Europe PMC
19212759
PubMed citation
Europe PMC
19217074
PubMed citation
Europe PMC
21295046
PubMed citation
Europe PMC
21914633
PubMed citation
Europe PMC
21956571
PubMed citation
Europe PMC
22117694
PubMed citation
Europe PMC
22128843
PubMed citation
Europe PMC
22266400
PubMed citation
Europe PMC
22280157
PubMed citation
Europe PMC
22362148
PubMed citation
Europe PMC
22369458
PubMed citation
Europe PMC
22445805
PubMed citation
Europe PMC
22465696
PubMed citation
Europe PMC
22486999
PubMed citation
Europe PMC
Last Modified
25 January 2016