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ChEBI
> Main
CHEBI:29656 - neomethymycin
Main
ChEBI Ontology
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ChEBI Name
neomethymycin
ChEBI ID
CHEBI:29656
Definition
A twelve-membered macrolide antibiotic that is biosynthesised by
Streptomyces venezuelae
.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C25H43NO7
Net Charge
0
Average Mass
469.61140
Monoisotopic Mass
469.30395
InChI
InChI=1S/C25H43NO7/c1-
13-
9-
10-
20(28)
14(2)
11-
15(3)
22(17(5)
24(30)
32-
23(13)
18(6)
27)
33-
25-
21(29)
19(26(7)
8)
12-
16(4)
31-
25/h9-
10,13-
19,21-
23,25,27,29H,11-
12H2,1-
8H3/b10-
9+/t13-
,14-
,15+,16-
,17-
,18-
,19+,21-
,22+,23+,25+/m1/s1
InChIKey
UEIVQYHYALXCBD-OTUJEKPESA-N
SMILES
C[C@@H]
(O)
[C@H]
1OC(=O)
[C@H]
(C)
[C@@H]
(O[C@@H]
2O[C@H]
(C)
C[C@@H]
([C@H]
2O)
N(C)
C)
[C@@H]
(C)
C[C@@H]
(C)
C(=O)
\C=C\[C@H]
1C
Roles Classification
Biological Role
(s):
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
(via
macrolide antibiotic
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
neomethymycin (
CHEBI:29656
)
has role
bacterial metabolite (
CHEBI:76969
)
neomethymycin (
CHEBI:29656
)
is a
enone (
CHEBI:51689
)
neomethymycin (
CHEBI:29656
)
is a
macrolide antibiotic (
CHEBI:25105
)
neomethymycin (
CHEBI:29656
)
is a
monosaccharide derivative (
CHEBI:63367
)
neomethymycin (
CHEBI:29656
)
is conjugate base of
neomethymycin(1+) (
CHEBI:77353
)
Incoming
neomethymycin(1+) (
CHEBI:77353
)
is conjugate acid of
neomethymycin (
CHEBI:29656
)
IUPAC Name
(3
R
,4
S
,5
S
,7
R
,9
E
,11
R
,12
S
)-
12-
[(1
R
)-
1-
hydroxyethyl]-
3,5,7,11-
tetramethyl-
2,8-
dioxooxacyclododec-
9-
en-
4-
yl 3,4,6-
trideoxy-
3-
(dimethylamino)-
β-
D
-
xylo
-
hexopyranoside
Manual Xrefs
Databases
C11995
KEGG COMPOUND
CPD-13833
MetaCyc
LMPK04000036
LIPID MAPS
View more database links
Registry Numbers
Types
Sources
1334300
Reaxys Registry Number
Reaxys
497-73-4
CAS Registry Number
KEGG COMPOUND
497-73-4
CAS Registry Number
ChemIDplus
Citations
Types
Sources
11720530
PubMed citation
Europe PMC
20695498
PubMed citation
Europe PMC
23866020
PubMed citation
Europe PMC
5439233
PubMed citation
Europe PMC
9831532
PubMed citation
Europe PMC
9873687
PubMed citation
Europe PMC
Last Modified
11 March 2014