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

被引:24
|
作者
Freitas, Rosana H. C. N. [1 ]
Cordeiro, Natalia M. [2 ]
Carvalho, Patricia R. [2 ]
Alves, Marina A. [1 ]
Guedes, Isabella A. [3 ]
Valerio, Tayna S. [2 ]
Dardenne, Laurent E. [3 ]
Lima, Lidia M. [1 ]
Barreiro, Eliezer J. [1 ]
Fernandes, Patricia D. [2 ]
Fraga, Carlos A. M. [1 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Ciencias Biomed, Lab Avaliacao & Sintese Subst Bioat LASSBio, Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, ICB, Lab Farmacol Dor & Inflamacao, Rio de Janeiro, Brazil
[3] Lab Nacl Comp Cient, GMMSB, Petropolis, Brazil
关键词
anti-inflammatory; ensemble docking; kinase inhibitor; N-acylhydrazone; p38; MAPK; ACTIVATED PROTEIN-KINASE; DERIVATIVES; DESIGN; PALBOCICLIB;
D O I
10.1111/cbdd.13085
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:391 / 397
页数:7
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