GV 104326

Known as: (4S,8S)-4-methoxy-(9R,lOS,12R)-lO-(l-hydroxyethyl)-11-0x0-1 azatricyclo[7.2.0.03,8]undec-2-enecarboxylate, GV-104326, GV104326 
 
National Institutes of Health

Papers overview

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2006
2006
STUDIES TOWARDS THE SYNTHESIS OF FEW BIOLOGICALLY ACTIVE CHIRAL y-BUTYROLACTONE BASED MOLECULES EMPLOYING 2HYDROXYCITRIC ACID… (More)
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2003
2003
The guanido group of arginine condenses with 1, Z-cyclohexanedione in alkaline aqueous medium to form a new a-amino acid. The… (More)
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1998
1998
The activity of sanfetrinem (previously GV104326), was assessed against 168 isolates of Streptococcus pneumoniae and 90 isolates… (More)
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1996
1996
The in vitro activity of the trinem sanfetrinem (formerly GV104326) (GV) was compared with that of vancomycin, ampicillin, and/or… (More)
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1996
1996
GV104326 is a novel tricyclic beta-lactam (a trinem or, formerly, tribactam). The in vitro activity of GV104326 was compared with… (More)
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1996
1996
Sanfetrinem, formerly GV104326, is a new trinem antimicrobial agent with extensive in vitro activity for a variety of different… (More)
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1995
1995
High-performance liquid chromatography (HPLC) was used in combination with radioactivity detection and mass spectrometry (MS) to… (More)
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1994
1994
GV104326 is the first member of a new class of antibiotics (tribactams) selected for development. It combines a particularly… (More)
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1967
1967
The guanido group of arginine condenses with 1, Z-cyclohexanedione in alkaline aqueous medium to form a new a-amino acid. The… (More)
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