Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C7H14O4 |
| Molecular Weight | 162.1837 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H](O)[C@H](O)[C@](C)(O)CC=O
InChI
InChIKey=JYAQWANEOPJVEY-LYFYHCNISA-N
InChI=1S/C7H14O4/c1-5(9)6(10)7(2,11)3-4-8/h4-6,9-11H,3H2,1-2H3/t5-,6-,7+/m0/s1
| Molecular Formula | C7H14O4 |
| Molecular Weight | 162.1837 |
| 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 |
|---|---|---|
| Fate of antibacterial spiramycin in river waters. | 2010-02 |
|
| Design and synthesis of pathway genes for polyketide biosynthesis. | 2009 |
|
| Characterization of the heterodimeric MegBIIa:MegBIIb aldo-keto reductase involved in the biosynthesis of L-mycarose from Micromonospora megalomicea. | 2007-07-10 |
|
| Substrate flexibility of vicenisaminyltransferase VinC involved in the biosynthesis of vicenistatin. | 2007-04-25 |
|
| The in vitro characterization of the erythronolide mycarosyltransferase EryBV and its utility in macrolide diversification. | 2007-03-05 |
|
| Bioassay-guided evolution of glycosylated macrolide antibiotics in Escherichia coli. | 2007-02 |
|
| A two-stage one-pot enzymatic synthesis of TDP-L-mycarose from thymidine and glucose-1-phosphate. | 2006-02-08 |
|
| Biosynthesis of TDP-l-mycarose: the specificity of a single enzyme governs the outcome of the pathway. | 2005-07-06 |
|
| Structural identification of bitespiramycin metabolites in rat: a single oral dose study. | 2005-04 |
|
| Acid catalysed degradation of some spiramycin derivatives found in the antibiotic bitespiramycin. | 2004-11-15 |
|
| Ketopremithramycins and ketomithramycins, four new aureolic acid-type compounds obtained upon inactivation of two genes involved in the biosynthesis of the deoxysugar moieties of the antitumor drug mithramycin by Streptomyces argillaceus, reveal novel insights into post-PKS tailoring steps of the mithramycin biosynthetic pathway. | 2002-02-27 |
|
| Isolation and structure elucidation of vicenistatin M, and importance of the vicenisamine aminosugar for exerting cytotoxicity of vicenistatin. | 2001-03 |
|
| The mtmVUC genes of the mithramycin gene cluster in Streptomyces argillaceus are involved in the biosynthesis of the sugar moieties. | 2001-02 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:39:25 GMT 2025
by
admin
on
Mon Mar 31 23:39:25 GMT 2025
|
| Record UNII |
I71I3DG1W1
|
| Record Status |
Validated (UNII)
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| Record Version |
|
-
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| Code System | Code | Type | Description | ||
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I71I3DG1W1
Created by
admin on Mon Mar 31 23:39:25 GMT 2025 , Edited by admin on Mon Mar 31 23:39:25 GMT 2025
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PRIMARY | |||
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92345-04-5
Created by
admin on Mon Mar 31 23:39:25 GMT 2025 , Edited by admin on Mon Mar 31 23:39:25 GMT 2025
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PRIMARY |