1. Academic Validation
  2. HMG-CoA Reductase inhibitors: an updated review of patents of novel compounds and formulations (2011-2015)

HMG-CoA Reductase inhibitors: an updated review of patents of novel compounds and formulations (2011-2015)

  • Expert Opin Ther Pat. 2016 Nov;26(11):1257-1272. doi: 10.1080/13543776.2016.1216977.
Eduardo Filipe Oliveira 1 Diogo Santos-Martins 1 António Meireles Ribeiro 1 Natércia Fernandes Brás 1 Nuno Sousa Cerqueira 1 Sérgio Filipe Sousa 1 Maria João Ramos 1 Pedro Alexandrino Fernandes 1
Affiliations

Affiliation

  • 1 a UCIBIO@REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências , Universidade do Porto , Porto , Portugal.
Abstract

Statins are remarkably safe and efficient medications that are the mainstay of hypercholesterolemia treatment and have proven to be an invaluable tool to lower the risk of acute cardiovascular events. These compounds are inhibitors of 3-hydroxy-methylglutaryl CoA reductase (HMG-R), the rate-limiting Enzyme in Cholesterol biosynthesis. In spite of their success, they present undesirable side effects and are now loosing patent protection, which provides a great opportunity for the development of new and improved statins. Areas covered: This review summarizes the new patents for HMG-R inhibitors for the 2011-2015 period. Combinations of existing statins with other drugs are also addressed, as well as novel applications of existing statins. Expert opinion: Recent efforts for the discovery of HMG-CoA-R inhibitors has resulted in several new molecules. Most of these are based on commercially available statins, including sterol and terpenoid derivatives. A few Peptides have also been patented. However, the origin of the side effects caused by previous statins continues to be, to a large extent, unknown. Although the patents published in the past 5 years are promising, and might result in new drugs, there is still no way to know if they will present reduced toxicity. Only future clinical trials will answer this question.

Keywords

HMG-R; Statins; cardiovascular diseases; formulations; new chemical entities; sterols; terpenoids.

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