Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C8H16O4 |
| Molecular Weight | 176.2106 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CO[C@](C)(CC=O)[C@@H](O)[C@H](C)O
InChI
InChIKey=AJSDVNKVGFVAQU-BIIVOSGPSA-N
InChI=1S/C8H16O4/c1-6(10)7(11)8(2,12-3)4-5-9/h5-7,10-11H,4H2,1-3H3/t6-,7-,8+/m0/s1
| Molecular Formula | C8H16O4 |
| Molecular Weight | 176.2106 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Various novel erythromycin derivatives obtained by different modifications: recent advance in macrolide antibiotics. | 2010-04 |
|
| Structure-activity relationships of macrolides against Mycobacterium tuberculosis. | 2008-08 |
|
| Mechanism for the degradation of erythromycin A and erythromycin A 2'-ethyl succinate in acidic aqueous solution. | 2007-10-11 |
|
| Systematic approach to understanding macrolide-ribosome interactions: NMR and modeling studies of oleandomycin and its derivatives. | 2006-01-19 |
|
| Accelerated transformation and deactivation of erythromycin in superheated water. 2. Transformation reactions and bioassays. | 2005-04-01 |
|
| pH-dependent geometric isomerization of roxithromycin in simulated gastrointestinal fluids and in rats. | 2004-05 |
|
| Rapid and accurate prediction of degradant formation rates in pharmaceutical formulations using high-performance liquid chromatography-mass spectrometry. | 2004-04 |
|
| Nonpeptide luteinizing hormone-releasing hormone antagonists derived from erythromycin A: design, synthesis, and biological activity of cladinose replacement analogues. | 2004-02-26 |
|
| Synthesis, stereochemical assignment and biological activity of a novel series of C-4" modified aza-macrolides. | 2003-06-16 |
|
| Dead bugs don't mutate: susceptibility issues in the emergence of bacterial resistance. | 2003-01 |
|
| Regioselective synthesis of bifunctional macrolides for probing ribosomal binding. | 2002-03-21 |
|
| [Multicenter study in southern South America of the in vitro activity of telithromycin in strains with defined resistance phenotypes isolated from community-acquired respiratory infections]. | 2001-09 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Tue Apr 01 16:21:29 GMT 2025
by
admin
on
Tue Apr 01 16:21:29 GMT 2025
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| Record UNII |
1C99S1OM20
|
| Record Status |
FAILED
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| Record Version |
|
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1C99S1OM20
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5460588
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