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ChEBI
> Main
CHEBI:16298 -
D
-mannitol 1-phosphate
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ChEBI Name
D
-mannitol 1-phosphate
ChEBI ID
CHEBI:16298
ChEBI ASCII Name
D-mannitol 1-phosphate
Definition
An alditol 1-phosphate that is the 1-
O
-phospho derivative of mannitol with
D
-configuration.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:12997, CHEBI:4205, CHEBI:21051
Supplier Information
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Molfile
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Molfile
Formula
C6H15O9P
Net Charge
0
Average Mass
262.15170
Monoisotopic Mass
262.04537
InChI
InChI=1S/C6H15O9P/c7-
1-
3(8)
5(10)
6(11)
4(9)
2-
15-
16(12,13)
14/h3-
11H,1-
2H2,(H2,12,13,14)
/t3-
,4-
,5-
,6-
/m1/s1
InChIKey
GACTWZZMVMUKNG-KVTDHHQDSA-N
SMILES
OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)COP(O)(O)=O
Metabolite of Species
Details
Escherichia coli
(NCBI:txid562)
See:
PubMed
Roles Classification
Biological Role
(s):
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in
Escherichia coli
.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
D
-mannitol 1-phosphate (
CHEBI:16298
)
has functional parent
D
-mannitol (
CHEBI:16899
)
D
-mannitol 1-phosphate (
CHEBI:16298
)
has role
Escherichia coli
metabolite (
CHEBI:76971
)
D
-mannitol 1-phosphate (
CHEBI:16298
)
has role
human metabolite (
CHEBI:77746
)
D
-mannitol 1-phosphate (
CHEBI:16298
)
is a
alditol 1-phosphate (
CHEBI:22292
)
D
-mannitol 1-phosphate (
CHEBI:16298
)
is a
hexitol phosphate (
CHEBI:24582
)
D
-mannitol 1-phosphate (
CHEBI:16298
)
is conjugate acid of
D
-mannitol 1-phosphate(2−) (
CHEBI:61381
)
Incoming
D
-mannitol 1-phosphate(2−) (
CHEBI:61381
)
is conjugate base of
D
-mannitol 1-phosphate (
CHEBI:16298
)
IUPAC Names
1-
O
-phosphono-
D
-mannitol
D
-mannitol 1-(dihydrogen phosphate)
Synonym
Source
D-Mannitol 1-phosphate
KEGG COMPOUND
Manual Xrefs
Databases
C00019638
KNApSAcK
C00644
KEGG COMPOUND
HMDB0001530
HMDB
MANNITOL-1P
MetaCyc
View more database links
Registry Numbers
Types
Sources
15806-48-1
CAS Registry Number
ChemIDplus
1728362
Reaxys Registry Number
Reaxys
Citation
Type
Source
21299839
PubMed citation
Europe PMC
Last Modified
25 January 2016