Synthesis and Therapeutic Effect of New Cis-Platinum Complexes on Experimental Tumors

  • R. Voegeli
  • J. Pohl
  • P. Hilgard
  • J. Engel
  • W. Schumacher
  • H. Brunner
  • M. Schmidt
  • U. Holzinger
  • H. Schönenberger
Part of the Developments in Oncology book series (DION, volume 54)

Abstract

The substitution of the two NH3 groups in cisplatinum (cDDP) by ethylene diamine ligands leads to complexes with good pharmacological activity against experimental tumors (1). Our aim was to increase the activity/toxicity ratio and also to provide compounds against tumors which are either nonresponsive or resistant to cisplatinum. We prepared new platinum complexes of 1,2-diaminoethanes derived from phenylalanine.

Keywords

Mammary Tumor L1210 Cell Test Substance Urea Concentration Thionyl Chloride 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Literature

  1. 1.
    Brunner, H., Schmidt, M., Unger, G. and Schoenenberger H. Eur. J. Med. Chem. — Chim. Ther. 20:509-512, 1985.Google Scholar

Copyright information

© Martinus Nijhoff Publishing, Boston 1988

Authors and Affiliations

  • R. Voegeli
  • J. Pohl
  • P. Hilgard
  • J. Engel
  • W. Schumacher
  • H. Brunner
  • M. Schmidt
  • U. Holzinger
  • H. Schönenberger

There are no affiliations available

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