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InChI=1S/CH4O/c1-2/h2H,1H3
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caffeine
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ChEBI
> Main
CHEBI:41582 -
D
-pipecolic acid
Main
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ChEBI Name
D
-pipecolic acid
ChEBI ID
CHEBI:41582
ChEBI ASCII Name
D-pipecolic acid
Definition
The
D
-enantiomer of pipecolic acid.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:18704, CHEBI:41574
Supplier Information
Download
Molfile
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Molfile
Formula
C6H11NO2
Net Charge
0
Average Mass
129.157
Monoisotopic Mass
129.07898
InChI
InChI=1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)/t5-/m1/s1
InChIKey
HXEACLLIILLPRG-RXMQYKEDSA-N
SMILES
N1CCCC[C@@H]1C(O)=O
Metabolite of Species
Details
Homo sapiens
(NCBI:txid9606)
See:
PubMed
Roles Classification
Chemical Role
(s):
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
Biological Role
(s):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-pipecolic acid (
CHEBI:41582
)
has role
human metabolite (
CHEBI:77746
)
D
-pipecolic acid (
CHEBI:41582
)
is a
pipecolic acid (
CHEBI:17964
)
D
-pipecolic acid (
CHEBI:41582
)
is conjugate base of
D
-pipecolate (
CHEBI:18703
)
D
-pipecolic acid (
CHEBI:41582
)
is enantiomer of
L
-pipecolic acid (
CHEBI:30913
)
Incoming
D
-pipecolate (
CHEBI:18703
)
is conjugate acid of
D
-pipecolic acid (
CHEBI:41582
)
L
-pipecolic acid (
CHEBI:30913
)
is enantiomer of
D
-pipecolic acid (
CHEBI:41582
)
IUPAC Name
(2
R
)-piperidine-2-carboxylic acid
Synonyms
Sources
(
R
)-pipecolic acid
ChEBI
(
R
)-piperidine-2-carboxylic acid
ChemIDplus
6-CARBOXYPIPERIDINE
PDBeChem
Manual Xrefs
Databases
CPI
PDBeChem
HMDB0005960
HMDB
View more database links
Registry Numbers
Types
Sources
1723-00-8
CAS Registry Number
ChemIDplus
4291592
Beilstein Registry Number
Beilstein
81094
Beilstein Registry Number
Beilstein
81094
Reaxys Registry Number
Reaxys
Citations
Types
Sources
24114978
PubMed citation
Europe PMC
2871866
PubMed citation
Europe PMC
Last Modified
19 July 2018