金属蛋白
化学
计算生物学
生物化学
酶
药理学
医学
生物
作者
Yang Yang,Xueqin Hu,Qing‐Shan Li,Xingxing Zhang,Ban‐Feng Ruan,Jun Xu,Chenzhong Liao
标识
DOI:10.2174/1568026615666150813145218
摘要
Metalloproteins have attracted momentous attentions for the treatment of many human diseases, including cancer, HIV, hypertension, etc. This article reviews the progresses that have been made in the field of drug development of metalloprotein inhibitors, putting emphasis on the targets of carbonic anhydrase, histone deacetylase, angiotensin converting enzyme, and HIV-1 integrase. Many other important metalloproteins are also briefly discussed. The binding and coordination modes of different marketed metalloprotein inhibitors are stated, providing insights to design novel metal binding groups and further novel inhibitors for metalloproteins. Keywords: Chelating, Drug design, Drug development, Magnesium, Metalloprotein, Zinc.
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