Department of Pharmaceutical Chemistry, School of Pharmaceutical Sciences, Shoolini University, Solan, Himachal Pradesh, 173 229, India.
Department of Science and Drug Technology, University of Torino, via Pietro Giuria 9, 10125, Torino, Italy.
Eur J Med Chem. 2023 Jun 5;254:115337. doi: 10.1016/j.ejmech.2023.115337. Epub 2023 Apr 6.
Cancer is a leading cause of death worldwide and there are still limited options for cure. Chemotherapy is the most significant treatment for cancer which increased survival rates, despite this, it is associated with numerous side effects, as well as cancer relapsing due to drug resistance insurgence; consequently, it is still a challenging task to develop new potent and less toxic anti-cancer agents for patients' care. Phenothiazine moiety, which leads a class of well-known antipsychotic drugs, possesses a wide range of biological activities and has been also introduced in cancer chemotherapy. This review aims in disclosing the use of phenothiazines during the last five years for the development of different anti-cancer drug candidates. The design and the synthetic strategies adopted, the SAR investigations and the role of reviewed phenothiazine derivatives as anti-cancer agents and multi-drug resistance (MDR) reversals are here fully described and discussed.
癌症是全球主要死因之一,目前治愈方法仍然有限。化疗是癌症治疗的最重要手段之一,它提高了生存率,但它也与许多副作用以及由于耐药性的出现导致癌症复发有关;因此,为患者开发新的有效且毒性较低的抗癌药物仍然是一项具有挑战性的任务。吩噻嗪部分是一类著名的抗精神病药物,具有广泛的生物活性,并已被引入癌症化疗中。本综述旨在揭示在过去五年中,吩噻嗪类化合物在开发不同的抗癌候选药物方面的应用。这里全面描述和讨论了所采用的设计和合成策略、SAR 研究以及被综述的吩噻嗪衍生物作为抗癌剂和多药耐药(MDR)逆转剂的作用。