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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:134538 -
D
-lyxonic acid
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ChEBI Name
D
-lyxonic acid
ChEBI ID
CHEBI:134538
ChEBI ASCII Name
D-lyxonic acid
Definition
A lyxonic acid that has
D
-configuration.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C5H10O6
Net Charge
0
Average Mass
166.129
Monoisotopic Mass
166.04774
InChI
InChI=1S/C5H10O6/c6-1-2(7)3(8)4(9)5(10)11/h2-4,6-9H,1H2,(H,10,11)/t2-,3+,4+/m1/s1
InChIKey
QXKAIJAYHKCRRA-UZBSEBFBSA-N
SMILES
C([C@H]([C@@H]([C@@H](C(=O)O)O)O)O)O
Metabolite of Species
Details
Arabidopsis thaliana
(NCBI:txid3702)
See:
MetaboLights Study
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):
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-lyxonic acid (
CHEBI:134538
)
has role
plant metabolite (
CHEBI:76924
)
D
-lyxonic acid (
CHEBI:134538
)
is a
lyxonic acid (
CHEBI:145755
)
D
-lyxonic acid (
CHEBI:134538
)
is conjugate acid of
D
-lyxonate (
CHEBI:145758
)
D
-lyxonic acid (
CHEBI:134538
)
is enantiomer of
L
-lyxonic acid (
CHEBI:6268
)
Incoming
D
-lyxono-1,4-lactone (
CHEBI:134539
)
has functional parent
D
-lyxonic acid (
CHEBI:134538
)
D
-lyxonate (
CHEBI:145758
)
is conjugate base of
D
-lyxonic acid (
CHEBI:134538
)
L
-lyxonic acid (
CHEBI:6268
)
is enantiomer of
D
-lyxonic acid (
CHEBI:134538
)
IUPAC Name
D
-lyxonic acid
Synonyms
Sources
(2
S
,3
S
,4
R
)-2,3,4,5-tetrahydroxypentanoic acid
IUPAC
Lyxonic acid
ChemIDplus
Manual Xrefs
Databases
134810
ChemSpider
CN1602762
Patent
CPD-8902
MetaCyc
GB2403220
Patent
US2004131737
Patent
View more database links
Registry Numbers
Types
Sources
1724266
Reaxys Registry Number
Reaxys
28223-40-7
CAS Registry Number
ChemIDplus
Citations
Types
Sources
11841815
PubMed citation
Europe PMC
22541300
PubMed citation
Europe PMC
Last Modified
08 January 2020