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  • tool
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  • Assistant Professor
  • Associate Professor
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  • Clinical Research Nurse
  • Clinician Researcher
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  • Pharmacist
  • PhD Student
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  • Post-doc
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  • Research Engineer
  • Retired scientist
  • Technician
  • Undergraduate Student
  • Veterinary
  • Visiting Scientist
  • Deputy Director of Center
  • Deputy Director of Department
  • Deputy Director of National Reference Center
  • Deputy Head of Facility
  • Director of Center
  • Director of Department
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© Research
Publication : Drugs under experimental and clinical research

Rational design of bis-intercalating drugs as antitumour agents: importance of rigidity in the linking chain

Scientific Fields
Diseases
Organisms
Applications
Technique

Published in Drugs under experimental and clinical research - 01 Jan 1987

Garbay-Jaureguiberry C, Esnault C, Delepierre M, Laugaa P, Laalami S, Le Pecq JB, Roques BP

Link to Pubmed [PMID] – 3652924

Drugs Exp Clin Res 1987;13(6):353-7

Ditercalinium (NSC 366241), a dimer of 10-methoxy-7H-pyrido[4,3-c]carbazole quaternarized on the pyridine nitrogen by a rigid bis(1,1′-ethyl)-4,4′-bipiperidine linking chain, is endowed with antitumour properties and bis-intercalates with high affinity into DNA. New dimers have been designed in the same series to evaluate the importance of the rigidity of the linking chain for pharmacological activity. The dimers, characterized by one and two additional methylene groups between the two piperidine rings of the linking chain, remain as active as ditercalinium. However, a third additional CH2 group between the two piperidine rings leads to an inactive dimer. Relationships between the different pharmacological activities of the drugs and their intercalation complexes with DNA were investigated using viscosimetry, absorption spectroscopy and NMR analyses.