Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C8H16O4 |
| Molecular Weight | 176.2102 |
| 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 | 176.2102 |
| 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 |
|---|---|---|
| Regioselective synthesis of bifunctional macrolides for probing ribosomal binding. | 2002 Mar 21 |
|
| Dead bugs don't mutate: susceptibility issues in the emergence of bacterial resistance. | 2003 Jan |
|
| Synthesis, stereochemical assignment and biological activity of a novel series of C-4" modified aza-macrolides. | 2003 Jun 16 |
|
| Rapid and accurate prediction of degradant formation rates in pharmaceutical formulations using high-performance liquid chromatography-mass spectrometry. | 2004 Apr |
|
| Nonpeptide luteinizing hormone-releasing hormone antagonists derived from erythromycin A: design, synthesis, and biological activity of cladinose replacement analogues. | 2004 Feb 26 |
|
| pH-dependent geometric isomerization of roxithromycin in simulated gastrointestinal fluids and in rats. | 2004 May |
|
| Accelerated transformation and deactivation of erythromycin in superheated water. 2. Transformation reactions and bioassays. | 2005 Apr 1 |
|
| Systematic approach to understanding macrolide-ribosome interactions: NMR and modeling studies of oleandomycin and its derivatives. | 2006 Jan 19 |
|
| Mechanism for the degradation of erythromycin A and erythromycin A 2'-ethyl succinate in acidic aqueous solution. | 2007 Oct 11 |
|
| Various novel erythromycin derivatives obtained by different modifications: recent advance in macrolide antibiotics. | 2010 Apr |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:20:59 GMT 2023
by
admin
on
Sat Dec 16 11:20:59 GMT 2023
|
| Record UNII |
1C99S1OM20
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
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3758-45-0
Created by
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1C99S1OM20
Created by
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5460588
Created by
admin on Sat Dec 16 11:20:59 GMT 2023 , Edited by admin on Sat Dec 16 11:20:59 GMT 2023
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29612
Created by
admin on Sat Dec 16 11:20:59 GMT 2023 , Edited by admin on Sat Dec 16 11:20:59 GMT 2023
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