Substance
ID:449287
Names and Identifiers
IUPAC name
(2S,5R,6R)-6-amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
IUPAC Traditional name
(2S,5R,6R)-6-amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
Synonyms
Aminopenicillanic
acid
Registration numbers
CAS Number
Properties
Product Information
Application(s)
Antibiotic against
Proteus mirabilis, Escherichia coli and Staphylococcus aureus
Biological Source
Prod. by enzymic hydrol. of benzyl- or phenoxymethylpenicillins.
Also prod. as metab. prod. of several penicillin-producing fungi, esp. when side-chain precursors are absent.
Pharmacology Properties
Mechanism of Action
Lactamase inhibitor
Molecule Details
No Data Available
Click here to submit data
Molecular Spectra
No Data Available
Click here to submit data
References
• Aldrich Library of FT-IR Spectra, 1st edn., 1985, 1, 791C, (ir)
• Von Daehne, W. et al., J. Antibiot., 1980, 33, 451
• Huber, F. et al., Cephalosporins Penicillins: Chem. Biol., (Flynn, E.H., Ed.), Academic Press, 1972, 27, (rev)
• Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, PCU500
• Kirk-Othmer Encycl. Chem. Technol., 4th edn., Wiley, 1991, 3, 129, (rev)
• Aldrich Library of NMR Spectra, 2nd edn., 1983, 1, 664A, (nmr)
• Batchelor, R. et al., Nature (London), 1959, 183, 257, (manuf)
• Micetich, R.G. et al., Synthesis, 1976, 264, (oxide)
• Moore, B.A. et al., Antimicrob. Agents Chemother., 1984, 20, 327, (props)