COX inhibitors: a patent review (2011-2014)

被引:34
作者
Consalvi, Sara [1 ]
Biava, Mariangela [1 ]
Poce, Giovanna [1 ]
机构
[1] Univ Roma La Sapienza, Dipartimento Chim & Tecnol Farmaco, I-00185 Rome, Italy
关键词
anti-cancer agents; anti-inflammatory agents; COX inhibitors; COX; NSAIDs; ACID AMIDE HYDROLASE; SOLUBLE EPOXIDE HYDROLASE; NITRIC-OXIDE; 1,5-DIARYLPYRROLE SCAFFOLD; BIOLOGICAL EVALUATION; IN-VITRO; ENDOCANNABINOID OXYGENATION; EPOXYEICOSATRIENOIC ACIDS; PHARMACODYNAMIC HYBRIDS; SELECTIVE INHIBITOR;
D O I
10.1517/13543776.2015.1090973
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Introduction: The COX enzymes play a central role in the biosynthetic pathway of important biological mediators called prostanoids. Differences in regulation of gene expression, stability of transcripts and proteins determine the different biological functions of COX-1 and COX-2. While the COX-1 gene has been considered to be a housekeeping' gene expressed in many tissues and cells, COX-2 gene is upregulated during inflammation, hypoxia and in many cancers.Areas covered: The first part of this review provides a survey of the development of both modified traditional NSAIDs (tNSAIDs) and COX inhibitors (coxibs) with reduced side effects for the treatment of inflammation and cancer. The second part deals with patents reporting several dual inhibitors characterized by the conjugation of a COX-inhibitor scaffold to a molecule able to modulate a different target. Finally, two patents on novel COX inhibitor scaffolds are reported.Expert opinion: The most interesting branch of research concerns the conjugation of a COX-inhibitor scaffold to a molecule able to modulate a different target, in order to either enhance anti-inflammatory activity or to act as a dual inhibitor. Among the described compounds, selenium-containing coxibs inhibiting COX-2 and Akt, in addition to the multi-target biphenyl derivatives as dual inhibitors of COX and fatty acid amide hydrolase, are the most promising ones.
引用
收藏
页码:1357 / 1371
页数:15
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