Services
Research
Training
Industry
About us
ChEBI
Examples:
iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
Advanced
Home
Advanced Search
Browse
Documentation
Download
Tools
About ChEBI
Submit
Contact us
DiNA
Statistics
Entity of the Month
Periodic Table
Ontology
Train online
User Manual
Annotation Manual
Developer Manual
FAQ's
BiNChE
libChEBI
Web Services
ChEBI
> Main
CHEBI:134191 - 20-oxo-5-
O
-β-mycaminosyltylactone
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
20-oxo-5-
O
-β-mycaminosyltylactone
ChEBI ID
CHEBI:134191
ChEBI ASCII Name
20-oxo-5-O-beta-mycaminosyltylactone
Definition
A macrolide antibiotic that is 20-oxotylactone having a β-
D
-mycaminosyl residue attached at position 5.
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download
Molfile
XML
SDF
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
Formula
C31H51NO9
Net Charge
0
Average Mass
581.739
Monoisotopic Mass
581.35638
InChI
InChI=1S/C31H51NO9/c1-
9-
25-
19(4)
14-
17(2)
10-
11-
23(34)
18(3)
15-
22(12-
13-
33)
30(20(5)
24(35)
16-
26(36)
40-
25)
41-
31-
29(38)
27(32(7)
8)
28(37)
21(6)
39-
31/h10-
11,13-
14,18-
22,24-
25,27-
31,35,37-
38H,9,12,15-
16H2,1-
8H3/b11-
10+,17-
14+/t18-
,19+,20+,21-
,22+,24-
,25-
,27+,28-
,29-
,30-
,31+/m1/s1
InChIKey
FERSDKADYZRIAA-CQGKBTLCSA-N
SMILES
[C@@H]
1([C@H]
(C[C@H]
(C(C=CC(=C[C@@H]
([C@H]
(OC(C[C@H]
([C@@H]
1C)
O)
=O)
CC)
C)
C)
=O)
C)
CC=O)
O[C@H]
2[C@H]
(O)
[C@H]
([C@@H]
([C@H]
(O2)
C)
O)
N(C)
C
Metabolite of Species
Details
Mycobacterium avium
(NCBI:txid1764)
See:
PubMed
Apis cerana
(NCBI:txid7461)
See:
MetaboLights Study
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.
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
20-oxo-5-
O
-β-mycaminosyltylactone (
CHEBI:134191
)
has functional parent
tylactone (
CHEBI:29700
)
20-oxo-5-
O
-β-mycaminosyltylactone (
CHEBI:134191
)
has role
bacterial metabolite (
CHEBI:76969
)
20-oxo-5-
O
-β-mycaminosyltylactone (
CHEBI:134191
)
is a
aldehyde (
CHEBI:17478
)
20-oxo-5-
O
-β-mycaminosyltylactone (
CHEBI:134191
)
is a
enone (
CHEBI:51689
)
20-oxo-5-
O
-β-mycaminosyltylactone (
CHEBI:134191
)
is a
macrolide antibiotic (
CHEBI:25105
)
20-oxo-5-
O
-β-mycaminosyltylactone (
CHEBI:134191
)
is a
monosaccharide derivative (
CHEBI:63367
)
20-oxo-5-
O
-β-mycaminosyltylactone (
CHEBI:134191
)
is a
tertiary amino compound (
CHEBI:50996
)
IUPAC Name
(4
R
,5
S
,6
S
,7
R
,9
R
,11
E
,13
E
,15
S
,16
R
)-
16-
ethyl-
4-
hydroxy-
5,9,13,15-
tetramethyl-
2,10-
dioxo-
7-
(2-
oxoethyl)-
1-
oxacyclohexadeca-
11,13-
dien-
6-
yl 3,6-
dideoxy-
3-
(dimethylamino)-
β-
D
-
glucopyranoside
Synonyms
Sources
23-Deoxy-5-O-beta-mycaminosyltylonolide
KEGG COMPOUND
23-Deoxy-5-O-mycaminosyltylonolide
ChemIDplus
Deepoxycirramycin A1
ChemIDplus
Manual Xrefs
Databases
C20760
KEGG COMPOUND
CPD-15945
MetaCyc
US4334019
Patent
View more database links
Registry Numbers
Types
Sources
50507-46-5
CAS Registry Number
ChemIDplus
6457636
Reaxys Registry Number
Reaxys
Citation
Type
Source
2817858
PubMed citation
Europe PMC
Last Modified
13 June 2017