Boron in drug design: Recent advances in the development of new therapeutic agents

被引:160
|
作者
Santos Fernandes, Guilherme Felipe [1 ,2 ,3 ]
Denny, William Alexander [3 ]
Dos Santos, Jean Leandro [1 ]
机构
[1] Sao Paulo State Univ, Sch Pharmaceut Sci, BR-14800903 Araraquara, Brazil
[2] Sao Paulo State Univ, Inst Chem, BR-14800060 Araraquara, Brazil
[3] Univ Auckland, Fac Med & Hlth Sci, Auckland Canc Soc Res Ctr, Auckland, New Zealand
基金
巴西圣保罗研究基金会;
关键词
Boron; Drug design; Boron-containing compounds; Biological activity; Boronic acids; Benzoxaboroles; CXCR1/2 ANTAGONISTS OPTIMIZATION; ACID PROTEASOME INHIBITORS; SERINE BETA-LACTAMASES; IN-VIVO EVALUATION; MYCOBACTERIUM-TUBERCULOSIS; BIOLOGICAL EVALUATION; DEVELOPMENT CANDIDATE; CARBONIC-ANHYDRASES; LEAD OPTIMIZATION; EFFLUX PUMP;
D O I
10.1016/j.ejmech.2019.06.092
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Advances in the field of boron chemistry have expanded the application of this element in Medicinal Chemistry. Boron-containing compounds represent a new class for medicinal chemists to use in their drug designs. Bortezomib (Velcade (R)), a dipeptide boronic acid approved by the FDA in 2003 for treatment of multiple myeloma, paved the way for the discovery of new boron-containing compounds. After its approval, two other boron-containing compounds have been approved, tavaborole (Kerydin (R)) for the treatment of onychomicosis and crisaborole (Eucrisa (R)) for the treatment of mild to moderate atopic dermatitis. A number of boron-containing compounds have been described and evaluated for a plethora of therapeutic applications. The present review is intended to highlight the recent advances related to boron-containing compounds and their therapeutic applications. Here, we focused only in those most biologically active compounds with proven in vitro and/or in vivo efficacy in the therapeutic area published in the last years. (C) 2019 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:791 / 804
页数:14
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