.BETA.-Lactam antibiotics. I. Comparative structure-activity relationships of 6-acylaminopenicillanic acid derivatives and their 6-(D-.ALPHA.-acylaminophenylacetamido) penicillanic acid analogues.

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  • COMPARATIVE STRUCTURE-ACTIVITY RELATIONSHIPS OF 6-ACYLAMINOPENICILLANIC ACID DERIVATIVES AND THEIR 6-(D-α-ACYLAMINOPHENYLACETAMIDO) PENICILLANIC ACID ANALOGUES

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Structure-activity relationships were compared for two series of penicillins containing a common acyl group. In series I, which included most of the penicillins in clinical use, the acyl moiety was linked directly to the amino group of the penicillin nucleus. For series II the acyl moiety was linked to the amino group of D-α-aminobenzylpenicillin (ampicillin). In the majority of cases a striking similarity between the two series was observed. The correlation provided both a valuable means of classifying and predicting the antibacterial properties of one series from a knowledge of the other.

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Details 詳細情報について

  • CRID
    1390282679130312576
  • NII Article ID
    130003498800
  • DOI
    10.7164/antibiotics.27.922
  • COI
    1:CAS:528:DyaE2MXhtlent7Y%3D
  • ISSN
    18811469
    00218820
  • PubMed
    4219783
  • Text Lang
    en
  • Article Type
    journal article
  • Data Source
    • JaLC
    • Crossref
    • PubMed
    • CiNii Articles
  • Abstract License Flag
    Disallowed

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