| Literature DB >> 19327871 |
Maria Letícia de Castro Barbosa1, Gabriela Muniz de Albuquerque Melo, Yolanda Karla Cupertino da Silva, Raquel de Oliveira Lopes, Everton Tenório de Souza, Aline Cavalcanti de Queiroz, Salete Smaniotto, Magna Suzana Alexandre-Moreira, Eliezer J Barreiro, Lídia Moreira Lima.
Abstract
In this paper we report the design, synthesis and pharmacological evaluation of a series of N-phenyl-acetamide sulfonamide derivatives (5a-g), planned by structural modification on the prototype paracetamol (1). In this series (5a-g), compound LASSBio-1300 (5e; ID(50)=5.81 micromol/kg) stands out as a new non-hepatotoxic analgesic drug candidate. The increase of area, volume and electrostatic potential of paracetamol's analogues seems to be beneficial to the analgesic activity. Unlike paracetamol (1) and the other analogues (5a, 5d-g), compounds 5b and 5c presented an important anti-hypernociceptive activity associated to inflammatory pain.Entities:
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Year: 2009 PMID: 19327871 DOI: 10.1016/j.ejmech.2009.02.026
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514