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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:16313 -
D
-proline
Main
ChEBI Ontology
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ChEBI Name
D
-proline
ChEBI ID
CHEBI:16313
ChEBI ASCII Name
D-proline
Definition
The
D
-enantiomer of proline.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:42213, CHEBI:42129, CHEBI:45156, CHEBI:45161, CHEBI:42012, CHEBI:4226, CHEBI:13008, CHEBI:21070
Supplier Information
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Wikipedia
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Read full article at Wikipedia
Formulae
C5H9NO2
C5H9NO2
Net Charge
0
Average Mass
115.13050
Monoisotopic Mass
115.06333
InChI
InChI=1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/t4-/m1/s1
InChIKey
ONIBWKKTOPOVIA-SCSAIBSYSA-N
SMILES
OC(=O)[C@H]1CCCN1
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
Source: BioModels - MODEL1507180067 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):
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
(via
proline
)
Daphnia magna metabolite
A
Daphnia
metabolite produced by the species
Daphnia magna
.
(via
proline
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-proline (
CHEBI:16313
)
has role
mouse metabolite (
CHEBI:75771
)
D
-proline (
CHEBI:16313
)
is a
D
-α-amino acid (
CHEBI:16733
)
D
-proline (
CHEBI:16313
)
is a
proline (
CHEBI:26271
)
D
-proline (
CHEBI:16313
)
is conjugate acid of
D
-prolinate (
CHEBI:32867
)
D
-proline (
CHEBI:16313
)
is conjugate base of
D
-prolinium (
CHEBI:32868
)
D
-proline (
CHEBI:16313
)
is enantiomer of
L
-proline (
CHEBI:17203
)
D
-proline (
CHEBI:16313
)
is tautomer of
D
-proline zwitterion (
CHEBI:57726
)
Incoming
D
-proline derivative (
CHEBI:84185
)
has functional parent
D
-proline (
CHEBI:16313
)
D
-prolinium (
CHEBI:32868
)
is conjugate acid of
D
-proline (
CHEBI:16313
)
D
-prolinate (
CHEBI:32867
)
is conjugate base of
D
-proline (
CHEBI:16313
)
L
-proline (
CHEBI:17203
)
is enantiomer of
D
-proline (
CHEBI:16313
)
D
-proline residue (
CHEBI:30018
)
is substituent group from
D
-proline (
CHEBI:16313
)
D
-prolino group (
CHEBI:32870
)
is substituent group from
D
-proline (
CHEBI:16313
)
D
-prolyl group (
CHEBI:32869
)
is substituent group from
D
-proline (
CHEBI:16313
)
D
-proline zwitterion (
CHEBI:57726
)
is tautomer of
D
-proline (
CHEBI:16313
)
IUPAC Name
D
-proline
Synonyms
Sources
(2
R
)-pyrrolidine-2-carboxylic acid
IUPAC
(R)-2-Carboxypyrrolidine
HMDB
(
R
)-pyrrolidine-2-carboxylic acid
ChEBI
D
-Prolin
ChEBI
D-Proline
KEGG COMPOUND
D-PROLINE
PDBeChem
DPR
PDBeChem
Manual Xrefs
Databases
C00763
KEGG COMPOUND
D-proline
Wikipedia
D-PROLINE
MetaCyc
DB02853
DrugBank
DPR
PDBeChem
HMDB0003411
HMDB
View more database links
Registry Numbers
Types
Sources
344-25-2
CAS Registry Number
KEGG COMPOUND
344-25-2
CAS Registry Number
ChemIDplus
80811
Reaxys Registry Number
Reaxys
833984
Gmelin Registry Number
Gmelin
Citations
Types
Sources
19023642
PubMed citation
Europe PMC
20023020
PubMed citation
Europe PMC
20959625
PubMed citation
Europe PMC
21374575
PubMed citation
Europe PMC
21563681
PubMed citation
Europe PMC
22475019
PubMed citation
Europe PMC
22479580
PubMed citation
Europe PMC
Last Modified
27 January 2016