Department of Medicinal Chemistry, Bharati Vidyapeeth's College of Pharmacy, CBD-Belapur, Navi Mumbai-400614, Maharashtra, India.
Mini Rev Med Chem. 2010 Nov;10(13):1263-76. doi: 10.2174/13895575110091263.
Histone Deacetylases (HDACs) enzymes are critical in regulating gene expression and transcription. They also play a fundamental role in regulating cellular activities such as cell proliferation, survival and differentiation. Inhibition of HDACs has generated many fascinating results including a new strategy in human cancer therapy. HDAC Inhibitors (HDACIs) like SAHA, TSA are emerging as new promising drugs for various anti-inflammatory and CNS-disorders. This review, along with chemical classification, emphasizes on the therapeutic potential of various HDACIs against different diseases.
组蛋白去乙酰化酶(HDACs)酶在调节基因表达和转录中起着关键作用。它们在调节细胞活动方面也起着至关重要的作用,如细胞增殖、存活和分化。HDAC 的抑制产生了许多引人注目的结果,包括人类癌症治疗的新策略。SAHA、TSA 等 HDAC 抑制剂(HDACIs)作为各种抗炎和中枢神经系统疾病的新的有前途的药物正在出现。本综述结合化学分类,强调了各种 HDACIs 对不同疾病的治疗潜力。