Literature DB >> 5780394

Some active derivatives of penicillin.

L D Brown, W A Zygmunt, H E Stavely.   

Abstract

The antibacterial activities of a number of amide derivatives of penicillin against both penicillin-sensitive and penicillin-resistant cultures were determined. Several of them were found to possess significant inhibitory activity against certain gram-positive bacteria. The amides, although resistant to the destructive action of beta-lactamase, did not protect G in competitive experiments. One derivative, the O-benzylhydroxamide of penicillin G, was active against six or eight penicillin-resistant strains of Staphylococcus aureus (minimal inhibitory concentration, 0.2 mug/ml or less), but was found to have only a minimal in vivo activity against mouse Streptococcus infections.

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Year:  1969        PMID: 5780394      PMCID: PMC377689          DOI: 10.1128/am.17.3.339-343.1969

Source DB:  PubMed          Journal:  Appl Microbiol        ISSN: 0003-6919


  3 in total

1.  [Hydroxylamides of penicillin V].

Authors:  C Coronelli; G C Lancini; R Pallanza; G Tamoni; P Sensi
Journal:  Farmaco Sci       Date:  1966-06

2.  Glycopeptide transpeptidase and D-alanine carboxypeptidase: penicillin-sensitive enzymatic reactions.

Authors:  K Izaki; M Matsuhashi; J L Strominger
Journal:  Proc Natl Acad Sci U S A       Date:  1966-03       Impact factor: 11.205

3.  Penicillin: its basic site of action as an inhibitor of a peptide cross-linking reaction in cell wall mucopeptide synthesis.

Authors:  E M Wise; J T Park
Journal:  Proc Natl Acad Sci U S A       Date:  1965-07       Impact factor: 11.205

  3 in total
  2 in total

1.  Neutral β-Lactams Inactivate High Molecular Mass Penicillin-Binding Proteins of Class B1, Including PBP2a of MRSA.

Authors:  Kinjal Dave; Timothy Palzkill; R F Pratt
Journal:  ACS Med Chem Lett       Date:  2013-12-16       Impact factor: 4.345

2.  Studies at the ionizable position of cephalosporins and penicillins: hydroxamates as substitutes for the traditional carboxylate group.

Authors:  Mark W Majewski; Patricia A Miller; Marvin J Miller
Journal:  J Antibiot (Tokyo)       Date:  2016-12-21       Impact factor: 2.649

  2 in total

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