Ghosh Arun K, Bilcer Geoffrey, Schiltz Gary
Department of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Chicago, Illinois 60607, USA, Fax +1(312)9960431;
Synthesis (Stuttg). 2001;2001(15):2203-2229. doi: 10.1055/s-2001-18434.
The treatment of HIV and AIDS was revolutionized by the introduction of peptidomimetic aspartyl protease inhibitors. One of the major limitations of this type of therapy is that higher therapeutic doses are necessary because of the presence of 'peptide-like' features in the drugs. Therefore, adequate supplies and cost effective syntheses of these drugs are of utmost importance. To date, there are six protease inhibitors approved by the United States Food and Drug Administration (FDA) for the treatment of HIV and AIDS. This review focuses on the published syntheses of currently FDA approved HIV protease inhibitor drugs, their isosteres and ligands.
拟肽天冬氨酸蛋白酶抑制剂的引入彻底改变了HIV和艾滋病的治疗方法。这类疗法的一个主要局限性在于,由于药物中存在“肽样”特征,需要更高的治疗剂量。因此,这些药物的充足供应和具有成本效益的合成至关重要。迄今为止,有六种蛋白酶抑制剂已获美国食品药品监督管理局(FDA)批准用于治疗HIV和艾滋病。本综述着重介绍目前已获FDA批准的HIV蛋白酶抑制剂药物、它们的等排体和配体的已发表合成方法。