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ChEBI
> Main
CHEBI:16889 -
trans
-3-hydroxy-
L
-proline
Main
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ChEBI Name
trans
-3-hydroxy-
L
-proline
ChEBI ID
CHEBI:16889
ChEBI ASCII Name
trans-3-hydroxy-L-proline
Definition
The (3
S
)-
trans
-diastereomer of 3-hydroxy-
L
-proline.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:43308, CHEBI:12868, CHEBI:10730, CHEBI:27055, CHEBI:27067
Supplier Information
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Molfile
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Molfile
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Formula
C5H9NO3
Net Charge
0
Average Mass
131.131
Monoisotopic Mass
131.05824
InChI
InChI=1S/C5H9NO3/c7-3-1-2-6-4(3)5(8)9/h3-4,6-7H,1-2H2,(H,8,9)/t3-,4-/m0/s1
InChIKey
BJBUEDPLEOHJGE-IMJSIDKUSA-N
SMILES
[C@H]1([C@H](CCN1)O)C(O)=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):
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
trans
-3-hydroxy-
L
-proline (
CHEBI:16889
)
has role
metabolite (
CHEBI:25212
)
trans
-3-hydroxy-
L
-proline (
CHEBI:16889
)
is a
3-hydroxy-
L
-proline (
CHEBI:20056
)
trans
-3-hydroxy-
L
-proline (
CHEBI:16889
)
is tautomer of
trans
-3-hydroxy-
L
-proline zwitterion (
CHEBI:57938
)
Incoming
trans
-3-hydroxy-
L
-proline residue (
CHEBI:85428
)
is substituent group from
trans
-3-hydroxy-
L
-proline (
CHEBI:16889
)
trans
-3-hydroxy-
L
-proline zwitterion (
CHEBI:57938
)
is tautomer of
trans
-3-hydroxy-
L
-proline (
CHEBI:16889
)
IUPAC Name
(3
S
)-3-hydroxy-
L
-proline
Synonyms
Sources
(2
S
,3
S
)-3-hydroxypyrrolidine-2-carboxylic acid
ChEBI
3-trans-hydroxy-L-proline
ChEBI
L-threo-3-hydroxyproline
ChEBI
trans-3-hydroxy-L-proline
ChEBI
trans-L-3-hydroxyproline
ChEBI
trans-L-3-Hydroxyproline
KEGG COMPOUND
Manual Xrefs
Databases
C05147
KEGG COMPOUND
CPD-664
MetaCyc
HMDB0059659
HMDB
HY3
PDBeChem
View more database links
Registry Number
Type
Source
471959
Reaxys Registry Number
Reaxys
Citation
Type
Source
22770225
PubMed citation
Europe PMC
Last Modified
21 November 2019