Details
Stereochemistry | RACEMIC |
Molecular Formula | C11H16N2O4S |
Molecular Weight | 272.321 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]12CC(SCCN)=C(N1C(=O)[C@]2([H])[C@@H](C)O)C(O)=O
InChI
InChIKey=WKDDRNSBRWANNC-ATRFCDNQSA-N
InChI=1S/C11H16N2O4S/c1-5(14)8-6-4-7(18-3-2-12)9(11(16)17)13(6)10(8)15/h5-6,8,14H,2-4,12H2,1H3,(H,16,17)/t5-,6-,8-/m1/s1
Molecular Formula | C11H16N2O4S |
Molecular Weight | 272.321 |
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 |
---|---|---|
Recent developments in carbapenems. | 2002 Apr |
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Antibiotic resistance and molecular typing of Pseudomonas aeruginosa: focus on imipenem. | 2002 Feb |
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Carboxymethylproline synthase (CarB), an unusual carbon-carbon bond-forming enzyme of the crotonase superfamily involved in carbapenem biosynthesis. | 2004 Feb 20 |
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Regulation and biosynthesis of carbapenem antibiotics in bacteria. | 2005 Apr |
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Secretion systems for secondary metabolites: how producer cells send out messages of intercellular communication. | 2005 Jun |
|
Synthesis of regio- and stereoselectively deuterium-labelled derivatives of L-glutamate semialdehyde for studies on carbapenem biosynthesis. | 2009 Jul 7 |
|
Current status of carbapenem antibiotics. | 2010 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 07:56:07 GMT 2023
by
admin
on
Sat Dec 16 07:56:07 GMT 2023
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Record UNII |
EWR2GDB37H
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Record Status |
Validated (UNII)
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Record Version |
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-
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441128
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EWR2GDB37H
Created by
admin on Sat Dec 16 07:56:07 GMT 2023 , Edited by admin on Sat Dec 16 07:56:07 GMT 2023
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