A review of the molecular design and biological activities of RXR agonists

被引:53
作者
de Almeida, Nathalia Rodrigues [1 ]
Conda-Sheridan, Martin [1 ]
机构
[1] Univ Nebraska Med Ctr, Dept Pharmaceut Sci, 4040 Emile St,PDD 3026, Omaha, NE 68198 USA
基金
美国国家卫生研究院;
关键词
9-cis-retinoic acid; anticancer agent; bexarotene; retinoid X receptor; rexinoids; RETINOID-X-RECEPTOR; NUCLEAR RECEPTOR; 9-CIS-RETINOIC ACID; ESTROGEN-RECEPTOR; INDUCED HYPOTHYROIDISM; SELECTIVE LIGANDS; LIPOPHILIC DOMAIN; ABCA1; EXPRESSION; STRUCTURAL BASIS; GENE-EXPRESSION;
D O I
10.1002/med.21578
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
An attractive approach to combat disease is to target theregulation of cell function. At the heart of this task are nuclear receptors (NRs); which control functions such as gene transcription. Arguably, the key player in this regulatory machinery is the retinoid X receptor (RXR). This NR associates with a third of the NRs found in humans. Scientists have hypothesized that controlling the activity of RXR is an attractive approach to control cellular functions that modulate diseases such as cancer, diabetes, Alzheimer's disease and Parkinson's disease. In this review, we will describe the key features of the RXR, present a historic perspective of the first RXR agonists, and discuss various templates that have been reported to activate RXR with a focus on their molecular structure, biological activity, and limitations. Finally, we will present an outlook of the field and future directions and considerations to synthesize or modulate RXR agonists to make these compounds a clinical reality.
引用
收藏
页码:1372 / 1397
页数:26
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