Cairo University, Faculty of Science, Department of Chemistry, Giza 12613, Egypt.
Expert Opin Ther Pat. 2013 Sep;23(9):1133-56. doi: 10.1517/13543776.2013.801455. Epub 2013 May 17.
Benzofuran moiety constitutes the core of several interesting pharmacologically active natural products. Benzofurans are among feasible potent active inhibitors against many diseases, viruses, microbes, fungus and enzymes. Several series of therapeutically important synthetic and naturally occurring benzofuran-containing compounds are reported in this chapter.
The current chapter focuses on the recent applications of benzofuran scaffolds and their wide range of biological activities during 1999 - 2012. The pharmacological areas covered included anti-inflammatory, antitumor, cytotoxic, antimicrobial, antitubercular, antioxidant, antiplasmodial, trypanocidal and insecticidal activities as well as enzyme inhibitory, HCV and HIV inhibitory activities.
The results reported in the chapter indicate that some benzofuran derivatives may be useful as potent drugs. From the structure-activity relationship (SAR), the presence of certain functions like -OH, -OMe in the benzofuran derivatives contributed greatly in increasing the potency of their therapeutic activities when compared with standards. For example, presence of the -OH and -OMe have made some benzofuran compounds more potent HIV-RT inhibitory activity than the standard atevirdine, and more potent antitumor agent when compared with standards (fluorouracil, doxorubicin and cytarabine). In addition, the enzyme aromatase CYP19 inhibitory activity of benzofurans having -OH and -OMe were greater than that observed for the reference arimidex.
苯并呋喃部分构成了几种有趣的具有药理活性的天然产物的核心。苯并呋喃是许多疾病、病毒、微生物、真菌和酶的潜在有效活性抑制剂。本章报道了几类具有治疗意义的合成和天然苯并呋喃类化合物。
本章重点介绍了 1999 年至 2012 年苯并呋喃支架的最新应用及其广泛的生物活性。涵盖的药理领域包括抗炎、抗肿瘤、细胞毒性、抗菌、抗结核、抗氧化、抗疟原虫、杀锥虫和杀虫活性以及酶抑制、HCV 和 HIV 抑制活性。
本章报告的结果表明,一些苯并呋喃衍生物可能是有用的强效药物。从构效关系(SAR)来看,苯并呋喃衍生物中存在某些官能团,如-OH、-OMe,当与标准品相比时,极大地提高了其治疗活性的效力。例如,-OH 和-OMe 的存在使一些苯并呋喃化合物具有比标准药物(阿替韦啶)更强的 HIV-RT 抑制活性,并且比标准药物(氟尿嘧啶、阿霉素和阿糖胞苷)具有更强的抗肿瘤活性。此外,具有-OH 和-OMe 的苯并呋喃的芳香酶 CYP19 抑制活性大于参考药物阿那曲唑。