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ChEBI
> Main
CHEBI:6178 -
L
-arabinofuranose
Main
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ChEBI Name
L
-arabinofuranose
ChEBI ID
CHEBI:6178
ChEBI ASCII Name
L-arabinofuranose
Definition
The five-membered ring form of
L
-arabinose.
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Molfile
XML
SDF
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Molfile
Formula
C5H10O5
Net Charge
0
Average Mass
150.12990
Monoisotopic Mass
150.05282
InChI
InChI=1S/C5H10O5/c6-1-2-3(7)4(8)5(9)10-2/h2-9H,1H2/t2-,3-,4+,5?/m0/s1
InChIKey
HMFHBZSHGGEWLO-HWQSCIPKSA-N
SMILES
OC[C@@H]1OC(O)[C@H](O)[C@H]1O
Roles Classification
Biological Role
(s):
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (
Saccharomyces cerevisiae
).
(via
L-arabinose
)
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
(via
L-arabinose
)
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
L-arabinose
)
fundamental metabolite
Any metabolite produced by all living cells.
(via
arabinose
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
L
-arabinofuranose (
CHEBI:6178
)
is a
L
-arabinose (
CHEBI:30849
)
L
-arabinofuranose (
CHEBI:6178
)
is enantiomer of
D
-arabinofuranose (
CHEBI:79054
)
Incoming
β-
D
-Gal
p
-(1→3)-
L
-Ara
f
(
CHEBI:152218
)
has functional parent
L
-arabinofuranose (
CHEBI:6178
)
5-
O
-(
trans
-feruloyl)-
L
-arabinofuranose (
CHEBI:62281
)
has functional parent
L
-arabinofuranose (
CHEBI:6178
)
α-
L
-arabinofuranose (
CHEBI:28772
)
is a
L
-arabinofuranose (
CHEBI:6178
)
β-
L
-arabinofuranose (
CHEBI:28272
)
is a
L
-arabinofuranose (
CHEBI:6178
)
D
-arabinofuranose (
CHEBI:79054
)
is enantiomer of
L
-arabinofuranose (
CHEBI:6178
)
IUPAC Name
L
-arabinofuranose
Synonyms
Sources
L
-arabinofuranose
UniProt
L-Arabinofuranose
KEGG COMPOUND
WURCS=2.0/1,1,0/[a211h-1x_1-4]/1/
ChEBI
Manual Xrefs
Databases
C06115
KEGG COMPOUND
G37615KF
GlyTouCan
G37615KF
GlyGen
View more database links
Registry Number
Type
Source
1904880
Beilstein Registry Number
Beilstein
Citations
Types
Sources
11206446
PubMed citation
Europe PMC
17336832
PubMed citation
Europe PMC
22499274
PubMed citation
Europe PMC
22549013
PubMed citation
Europe PMC
24036380
PubMed citation
Europe PMC
Last Modified
07 April 2021