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Development of antitubercular compounds based on a 4-quinolylhydrazone scaffold. Further structure-activity relationship studies

  • S Gemma
  • , L Savini
  • , M Altarelli
  • , P Tripaldi
  • , L Chiasserini
  • , Ss Coccone
  • , V Kumar
  • , C Camodeca
  • , G Campiani
  • , E Novellino
  • , Sandra Clarizio
  • , Giovanni Delogu
  • , S. Butini

Risultato della ricerca: Contributo in rivistaArticolopeer review

Abstract

A series of 4-quinolylhydrazones was synthesized and tested in vitro against Mycobacterium tuberculosis. At a concentration of 6.25microg/mL, most of the newly synthesized compounds displayed 100% inhibitory activity against M. tuberculosis in cellular assays. Further screening allowed the identification of very potent antitubercular agents. Compound 4c was also tested in a time-course experiment and against mtb clinical isolates, displaying interesting results.
Lingua originaleInglese
pagine (da-a)6063-6072
Numero di pagine10
RivistaBIOORGANIC & MEDICINAL CHEMISTRY
Volume17
DOI
Stato di pubblicazionePubblicato - 2009

OSS delle Nazioni Unite

Questo processo contribuisce al raggiungimento dei seguenti obiettivi di sviluppo sostenibile

  1. SDG 3 - Salute e benessere
    SDG 3 Salute e benessere

Keywords

  • Animals
  • Antitubercular Agents
  • Cell Line
  • Cercopithecus aethiops
  • Hydrazones
  • Microbial Sensitivity Tests
  • Mycobacterium tuberculosis
  • Structure-Activity Relationship
  • Vero Cells

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