Ahmad Irshad
Department of Mathematics and Natural Sciences, School of Arts and Sciences, American University of Ras Al Khaimah, Ras Al Khaimah, United Arab Emirates.
Eur J Med Chem. 2015 Sep 18;102:375-86. doi: 10.1016/j.ejmech.2015.08.010. Epub 2015 Aug 8.
Aromatase, a cytochrome P450 enzyme complex present in breast tissues, plays a significant role in the biosynthesis of important endogenous estrogens from androgens. The source of estrogen production in breast cancer tissues is intra-tumoral aromatase, and inhibition of aromatase may inhibit the growth stimulation effect of estrogens in breast cancer tissues. Consequently, aromatase is considered a useful therapeutic target in the treatment and prevention of estrogen-dependent breast cancer. Recently, different natural products and synthetic compounds have been rapidly developed, studied, and evaluated for aromatase inhibitory activity. Aromatase inhibitors are classified into two categories on the basis of their chemical structures, i.e., steroidal and nonsteroidal aromatase inhibitors. This review highlights the synthetic steroidal and nonsteroidal aromatase inhibitors reported in the literature in the last few years and will aid medicinal chemists in the design and synthesis of novel and pharmacologically-potent aromatase inhibitors for the treatment of breast cancer.
芳香化酶是一种存在于乳腺组织中的细胞色素P450酶复合物,在雄激素生物合成重要内源性雌激素的过程中发挥着重要作用。乳腺癌组织中雌激素的产生来源是肿瘤内的芳香化酶,抑制芳香化酶可能会抑制雌激素对乳腺癌组织的生长刺激作用。因此,芳香化酶被认为是治疗和预防雌激素依赖性乳腺癌的一个有用的治疗靶点。近年来,不同的天然产物和合成化合物已被迅速开发、研究和评估其芳香化酶抑制活性。芳香化酶抑制剂根据其化学结构分为两类,即甾体类和非甾体类芳香化酶抑制剂。本综述重点介绍了过去几年文献中报道的合成甾体类和非甾体类芳香化酶抑制剂,将有助于药物化学家设计和合成用于治疗乳腺癌的新型且具有药理活性的芳香化酶抑制剂。