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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:7933 - paromamine
Main
ChEBI Ontology
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ChEBI Name
paromamine
ChEBI ID
CHEBI:7933
Definition
An aminoglycoside that is 4α,6α-diaminocyclohexane-1β,2α,3β-triol in which the
pro
-
R
hydroxy group has been converted into its 2-amino-α-
D
-glucoside derivative.
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Molfile
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Molfile
Formula
C12H25N3O7
Net Charge
0
Average Mass
323.34280
Monoisotopic Mass
323.16925
InChI
InChI=1S/C12H25N3O7/c13-
3-
1-
4(14)
11(10(20)
7(3)
17)
22-
12-
6(15)
9(19)
8(18)
5(2-
16)
21-
12/h3-
12,16-
20H,1-
2,13-
15H2/t3-
,4+,5-
,6-
,7+,8-
,9-
,10-
,11-
,12-
/m1/s1
InChIKey
JGSMDVGTXBPWIM-HKEUSBCWSA-N
SMILES
N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@H]1O
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
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
paromamine (
CHEBI:7933
)
has functional parent
α-
D
-glucose (
CHEBI:17925
)
paromamine (
CHEBI:7933
)
has functional parent
2-deoxystreptamine (
CHEBI:28295
)
paromamine (
CHEBI:7933
)
is a
aminoglycoside (
CHEBI:47779
)
paromamine (
CHEBI:7933
)
is a
primary amino compound (
CHEBI:50994
)
paromamine (
CHEBI:7933
)
is a
triamine (
CHEBI:38751
)
paromamine (
CHEBI:7933
)
is conjugate base of
paromamine(3+) (
CHEBI:65015
)
Incoming
6'-oxoparomamine (
CHEBI:65008
)
has functional parent
paromamine (
CHEBI:7933
)
paromamine(3+) (
CHEBI:65015
)
is conjugate acid of
paromamine (
CHEBI:7933
)
IUPAC Name
(1
R
,2
R
,3
S
,4
R
,6
S
)-
4,6-
diamino-
2,3-
dihydroxycyclohexyl 2-
amino-
2-
deoxy-
α-
D
-
glucopyranoside
Synonyms
Sources
(1
R
)-
O
4-(2-amino-2-deoxy-α-
D
-glucopyranosyl)-2-deoxy-streptamine
ChEBI
4-
O
-
(2-
amino-
2-
deoxy-
α-
D
-
glucopyranosyl)-
2-
deoxy-
D
-
streptamine
ChEBI
Neomycin D
KEGG COMPOUND
Paromamine
KEGG COMPOUND
Manual Xrefs
Databases
C01743
KEGG COMPOUND
CPD-14125
MetaCyc
View more database links
Registry Numbers
Types
Sources
26713
Reaxys Registry Number
Reaxys
534-47-4
CAS Registry Number
KEGG COMPOUND
534-47-4
CAS Registry Number
ChemIDplus
Citations
Types
Sources
17206729
PubMed citation
Europe PMC
19466609
PubMed citation
Europe PMC
4645948
PubMed citation
Europe PMC
5459627
PubMed citation
Europe PMC
6698890
PubMed citation
Europe PMC
Last Modified
28 April 2020