1. Academic Validation
  2. N-acylsulfonamides: Synthetic routes and biological potential in medicinal chemistry

N-acylsulfonamides: Synthetic routes and biological potential in medicinal chemistry

  • Chem Biol Drug Des. 2017 Dec;90(6):1094-1105. doi: 10.1111/cbdd.13043.
Alessandra Ammazzalorso 1 Barbara De Filippis 1 Letizia Giampietro 1 Rosa Amoroso 1
Affiliations

Affiliation

  • 1 Dipartimento di Farmacia, Università G. d'Annunzio, Chieti, Italy.
Abstract

Sulfonamide is a common structural motif in naturally occurring and synthetic medicinal compounds. The rising interest in sulfonamides and N-acyl derivatives is attested by the large number of drugs and lead compounds identified in last years, explored in different fields of medicinal chemistry and showing biological activity. Many acylsulfonamide derivatives were designed and synthesized as isosteres of carboxylic acids, being the characteristics of these functional groups very close. Starting from chemical routes to N-acylsulfonamides, this review explores compounds of pharmaceutical interest, developed as enzymatic inhibitors or targeting receptors.

Keywords

PPAR; acylsulfonamides; antiproliferative; bioisosteres; sulfonamides.

Figures
Products