4.4 Article

Discovery of naphthyl-N-acylhydrazone p38 MAPK inhibitors with in vivo anti-inflammatory and anti-TNF- activity

Journal

CHEMICAL BIOLOGY & DRUG DESIGN
Volume 91, Issue 2, Pages 391-397

Publisher

WILEY
DOI: 10.1111/cbdd.13085

Keywords

anti-inflammatory; ensemble docking; kinase inhibitor; N-acylhydrazone; p38 MAPK

Funding

  1. Fundacao Carlos Chagas Filho de Amparo a Pesquisa do Estado do Rio de Janeiro
  2. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico
  3. Instituto Nacional de Ciencia e Tecnologia de Farmacos e Medicamentos [465.249/2014]

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Protein kinases constitute attractive therapeutic targets for development of new prototypes to treat different chronic diseases. Several available drugs, like tinibs, are tyrosine kinase inhibitors; meanwhile, inhibitors of serine/threonine kinases, such as mitogen-activated protein kinase (MAPK), are still trying to overcome some problems in one of the steps of clinical development to become drugs. So, here we reported the synthesis, the in vitro kinase inhibitory profile, docking studies, and the evaluation of anti-inflammatory profile of new naphthyl-N-acylhydrazone derivatives using animal models. Although all tested compounds (3a-d) have been characterized as p38 MAPK inhibitors and have showed in vivo anti-inflammatory action, LASSBio-1824 (3b) presented the best performance as p38 MAPK inhibitor, with IC50=4.45m, and also demonstrated to be the most promising anti-inflammatory prototype, with good in vivo anti-TNF- profile after oral administration.

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