Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C11H16N2O4S |
Molecular Weight | 272.321 |
Optical Activity | UNSPECIFIED |
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
Approval Year
PubMed
Title | Date | PubMed |
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Recent developments in carbapenems. | 2002 Apr |
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The biosynthetic gene cluster for the beta-lactam carbapenem thienamycin in Streptomyces cattleya. | 2003 Apr |
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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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Involvement of nitrogen-containing compounds in beta-lactam biosynthesis and its control. | 2006 Apr-Jun |
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Empirical antibacterial drug discovery--foundation in natural products. | 2006 Mar 30 |
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Identification of transcriptional activators for thienamycin and cephamycin C biosynthetic genes within the thienamycin gene cluster from Streptomyces cattleya. | 2008 Aug |
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Evidence that thienamycin biosynthesis proceeds via C-5 epimerization: ThnE catalyzes the formation of (2S,5S)-trans-carboxymethylproline. | 2009 Jan 26 |
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Current status of carbapenem antibiotics. | 2010 |
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Non-heme iron oxygenases generate natural structural diversity in carbapenem antibiotics. | 2010 Jan 13 |
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Discovery of 3-formyl-tyrosine metabolites from Pseudoalteromonas tunicata through heterologous expression. | 2010 Jan 27 |
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DTXSID10975412
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m10736
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SUB22136
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WMW5I5964P
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441128
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100000085400
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THIENAMYCIN
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59995-64-1
Created by
admin on Sat Dec 16 08:42:26 GMT 2023 , Edited by admin on Sat Dec 16 08:42:26 GMT 2023
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SUBSTANCE RECORD