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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:16867 -
D
-methionine
Main
ChEBI Ontology
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Models
ChEBI Name
D
-methionine
ChEBI ID
CHEBI:16867
ChEBI ASCII Name
D-methionine
Definition
An optically active form of methionine having
D
-configuration.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:44071, CHEBI:4215, CHEBI:13005, CHEBI:21065
Supplier Information
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Formula
C5H11NO2S
Net Charge
0
Average Mass
149.21238
Monoisotopic Mass
149.05105
InChI
InChI=1S/C5H11NO2S/c1-9-3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)/t4-/m1/s1
InChIKey
FFEARJCKVFRZRR-SCSAIBSYSA-N
SMILES
CSCC[C@@H](N)C(O)=O
Metabolite of Species
Details
Saccharomyces cerevisiae
(NCBI:txid4932)
See:
PubMed
Escherichia coli
(NCBI:txid562)
See:
PubMed
Escherichia coli
(NCBI:txid562)
See:
PubMed
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):
algal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in algae including unicellular organisms like chlorella and diatoms to multicellular organisms like giant kelps and brown algae.
(via
methionine
)
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in
Escherichia coli
.
(via
methionine
)
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (
Saccharomyces cerevisiae
).
(via
methionine
)
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
(via
methionine
)
Daphnia magna metabolite
A
Daphnia
metabolite produced by the species
Daphnia magna
.
(via
methionine
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-methionine (
CHEBI:16867
)
is a
D
-α-amino acid (
CHEBI:16733
)
D
-methionine (
CHEBI:16867
)
is a
methionine (
CHEBI:16811
)
D
-methionine (
CHEBI:16867
)
is conjugate acid of
D
-methioninate (
CHEBI:32637
)
D
-methionine (
CHEBI:16867
)
is conjugate base of
D
-methioninium (
CHEBI:32638
)
D
-methionine (
CHEBI:16867
)
is enantiomer of
L
-methionine (
CHEBI:16643
)
D
-methionine (
CHEBI:16867
)
is tautomer of
D
-methionine zwitterion (
CHEBI:57932
)
Incoming
(
R
)-5-[2-(methylthio)ethyl]hydantoin (
CHEBI:137150
)
has functional parent
D
-methionine (
CHEBI:16867
)
D
-methionine derivative (
CHEBI:84122
)
has functional parent
D
-methionine (
CHEBI:16867
)
D
-methioninium (
CHEBI:32638
)
is conjugate acid of
D
-methionine (
CHEBI:16867
)
D
-methioninate (
CHEBI:32637
)
is conjugate base of
D
-methionine (
CHEBI:16867
)
L
-methionine (
CHEBI:16643
)
is enantiomer of
D
-methionine (
CHEBI:16867
)
D
-methionine residue (
CHEBI:29984
)
is substituent group from
D
-methionine (
CHEBI:16867
)
D
-methionino group (
CHEBI:32641
)
is substituent group from
D
-methionine (
CHEBI:16867
)
D
-methionyl group (
CHEBI:32640
)
is substituent group from
D
-methionine (
CHEBI:16867
)
D
-methionine zwitterion (
CHEBI:57932
)
is tautomer of
D
-methionine (
CHEBI:16867
)
IUPAC Name
D
-methionine
Synonyms
Sources
(2
R
)-2-amino-4-(methylsulfanyl)butanoic acid
IUPAC
(
R
)-2-amino-4-(methylthio)butanoic acid
JCBN
(
R
)-methionine
ChemIDplus
D-2-Amino-4-(methylthio)butyric acid
KEGG COMPOUND
D
-Methionin
ChEBI
D-Methionine
KEGG COMPOUND
D-METHIONINE
PDBeChem
MED
PDBeChem
Manual Xrefs
Databases
C00855
KEGG COMPOUND
CPD-218
MetaCyc
DB02893
DrugBank
ECMDB21203
ECMDB
MED
PDBeChem
YMDB00816
YMDB
View more database links
Registry Numbers
Types
Sources
1722293
Reaxys Registry Number
Reaxys
26934
Gmelin Registry Number
Gmelin
348-67-4
CAS Registry Number
KEGG COMPOUND
348-67-4
CAS Registry Number
ChemIDplus
348-67-4
CAS Registry Number
NIST Chemistry WebBook
Citations
Types
Sources
15375647
PubMed citation
Europe PMC
20431016
PubMed citation
Europe PMC
20872028
PubMed citation
Europe PMC
21480759
PubMed citation
Europe PMC
21750343
PubMed citation
Europe PMC
21924333
PubMed citation
Europe PMC
22192214
PubMed citation
Europe PMC
22304623
PubMed citation
Europe PMC
318639
PubMed citation
Europe PMC
Last Modified
19 July 2017