Institut des Biomolécules Max Mousseron (IBMM), UMR 5247 CNRS-UM1-UM2, Bâtiment de Recherche Max Mousseron, Ecole Nationale Supérieure de Chimie de Montpellier, 8 rue de l'Ecole Normale, 34296 Montpellier Cedex, France.
Bioorg Med Chem. 2013 Mar 15;21(6):1419-26. doi: 10.1016/j.bmc.2012.10.043. Epub 2012 Nov 10.
Targeting tumour associated carbonic anhydrase (CA, EC 4.2.1.1) isoforms IX and XII is now considered as a pertinent approach for the development of new cancer therapeutics against hypoxic tumours. In the last period, with the help of X-ray crystallography, much progress has been achieved for the drug-design of selective CA IX inhibitors, by considering the three main structural elements that govern both potency and selectivity, that is, a zinc binding group (ZBG), an organic scaffold, and one or more side chains substituting the scaffold. The use of sugar moiety in the structure of sulfonamide-based CA inhibitors (CAIs), has allowed the discovery of very potent CA IX inhibitors able to impair the growth of both primary tumors and metastases. The search for specific CA IX inhibitors by using the sugar approach has become an important research field, leading to sulfonamides, sulfamates, sulfamides and coumarins with excellent in vitro activity and relevant potency in vivo, in animal models of cancer. This paper will review the latest development in this hot topic.
靶向肿瘤相关碳酸酐rase(CA,EC 4.2.1.1)同工酶 IX 和 XII 现已被认为是开发针对缺氧肿瘤的新型癌症治疗方法的相关方法。在过去的一段时间里,借助 X 射线晶体学,通过考虑三个主要的结构元素,即锌结合基团(ZBG)、有机支架和取代支架的一个或多个侧链,在设计选择性 CAIX 抑制剂的药物方面取得了很大进展,这三个结构元素控制着药物的效力和选择性。在磺酰胺类碳酸酐酶抑制剂(CAIs)的结构中使用糖部分,已经发现了非常有效的 CAIX 抑制剂,能够抑制原发性肿瘤和转移瘤的生长。通过使用糖方法寻找特异性 CAIX 抑制剂已成为一个重要的研究领域,导致了磺酰胺、硫酸盐、磺酰胺和香豆素具有出色的体外活性和在癌症动物模型中的相关效力。本文将综述这一热门话题的最新进展。