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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:17459 -
D
-iditol
Main
ChEBI Ontology
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ChEBI Name
D
-iditol
ChEBI ID
CHEBI:17459
ChEBI ASCII Name
D-iditol
Definition
The
D
-enantiomer of iditol.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:4198, CHEBI:12993, CHEBI:21042
Supplier Information
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Molfile
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Molfile
Formula
C6H14O6
Net Charge
0
Average Mass
182.17176
Monoisotopic Mass
182.07904
InChI
InChI=1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4-,5+,6+/m1/s1
InChIKey
FBPFZTCFMRRESA-ZXXMMSQZSA-N
SMILES
OC[C@@H](O)[C@H](O)[C@@H](O)[C@H](O)CO
Roles Classification
Biological Role
(s):
fungal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-iditol (
CHEBI:17459
)
has role
fungal metabolite (
CHEBI:76946
)
D
-iditol (
CHEBI:17459
)
is a
iditol (
CHEBI:24766
)
D
-iditol (
CHEBI:17459
)
is enantiomer of
L
-iditol (
CHEBI:18202
)
Incoming
L
-iditol (
CHEBI:18202
)
is enantiomer of
D
-iditol (
CHEBI:17459
)
IUPAC Name
D
-iditol
Synonyms
Sources
(2
R
,3
S
,4
S
,5
R
)-hexane-1,2,3,4,5,6-hexol
IUPAC
D
-Idit
ChEBI
D-Iditol
KEGG COMPOUND
D
-iditol
UniProt
Manual Xrefs
Databases
C01489
KEGG COMPOUND
CPD-357
MetaCyc
View more database links
Registry Numbers
Types
Sources
1721905
Reaxys Registry Number
Reaxys
1721905
Beilstein Registry Number
Beilstein
25878-23-3
CAS Registry Number
KEGG COMPOUND
Citations
Types
Sources
16232515
PubMed citation
Europe PMC
18175917
PubMed citation
Europe PMC
Last Modified
24 March 2015