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ChEBI
> Main
CHEBI:131938 - validoxylamine A 7'-phosphate
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ChEBI Ontology
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ChEBI Name
validoxylamine A 7'-phosphate
ChEBI ID
CHEBI:131938
Definition
A cyclitol phosphate that is validoxylamine A carrying a single monophosphate substituent at position 7'.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C14H26NO11P
Net Charge
0
Average Mass
415.331
Monoisotopic Mass
415.12435
InChI
InChI=1S/C14H26NO11P/c16-
3-
5-
1-
7(11(19)
13(21)
9(5)
17)
15-
8-
2-
6(4-
26-
27(23,24)
25)
10(18)
14(22)
12(8)
20/h1,6-
22H,2-
4H2,(H2,23,24,25)
/t6-
,7+,8+,9-
,10-
,11+,12+,13+,14+/m1/s1
InChIKey
ZKSTYMJGEHZSFH-MBABXGOBSA-N
SMILES
C1[C@@H]([C@@H]([C@H]([C@@H]([C@H]1COP(O)(=O)O)O)O)O)N[C@@H]2[C@@H]([C@H]([C@@H](C(=C2)CO)O)O)O
Metabolite of Species
Details
Streptomyces hygroscopicus
subsp.
limoneus
(NCBI:txid264445)
See:
PubMed
Roles Classification
Chemical Role
(s):
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Biological Role
(s):
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
validoxylamine A 7'-phosphate (
CHEBI:131938
)
has role
bacterial metabolite (
CHEBI:76969
)
validoxylamine A 7'-phosphate (
CHEBI:131938
)
is a
amino cyclitol (
CHEBI:61689
)
validoxylamine A 7'-phosphate (
CHEBI:131938
)
is a
cyclitol phosphate (
CHEBI:23450
)
validoxylamine A 7'-phosphate (
CHEBI:131938
)
is a
secondary amino compound (
CHEBI:50995
)
validoxylamine A 7'-phosphate (
CHEBI:131938
)
is conjugate acid of
validoxylamine A 7'-phosphate(1−) (
CHEBI:111504
)
Incoming
validoxylamine A 7'-phosphate(1−) (
CHEBI:111504
)
is conjugate base of
validoxylamine A 7'-phosphate (
CHEBI:131938
)
IUPAC Name
[(1
R
,2
R
,3
S
,4
S
,5
S
)-
2,3,4-
trihydroxy-
5-
{[(1
S
,4
R
,5
S
,6
S
)-
4,5,6-
trihydroxy-
3-
(hydroxymethyl)cyclohex-
2-
en-
1-
yl]amino}cyclohexyl]methyl dihydrogen phosphate
Manual Xref
Database
CPD-18789
MetaCyc
View more database links
Registry Number
Type
Source
20199462
Reaxys Registry Number
Reaxys
Citations
Types
Sources
21766819
PubMed citation
Europe PMC
22384130
PubMed citation
Europe PMC
22961651
PubMed citation
Europe PMC
23028689
PubMed citation
Europe PMC
Last Modified
17 May 2016