Gattu Rohith, Ramesh Sanjay S, Nadigar Siddaram, D Channe Gowda, Ramesh Suhas
Postgraduate Department of Chemistry, JSS College of Arts, Commerce and Science, Ooty Road, Mysuru 570025, Karnataka, India.
Department of Studies in Chemistry, Manasagangotri, University of Mysore, Mysuru 570005, Karnataka, India.
Antibiotics (Basel). 2023 Mar 7;12(3):532. doi: 10.3390/antibiotics12030532.
Peptide-based drugs are gaining significant momentum in the modern drug discovery, which is witnessed by the approval of new drugs by the FDA in recent years. On the other hand, small molecules-based drugs are an integral part of drug development since the past several decades. Peptide-containing drugs are placed between small molecules and the biologics. Both the peptides as well as the small molecules (mainly heterocycles) pose several drawbacks as therapeutics despite their success in curing many diseases. This gap may be bridged by utilising the so called 'conjugation chemistry', in which both the partners are linked to one another through a stable chemical bond, and the resulting conjugates are found to possess attracting benefits, thus eliminating the stigma associated with the individual partners. Over the past decades, the field of molecular hybridisation has emerged to afford us new and efficient molecular architectures that have shown high promise in medicinal chemistry. Taking advantage of this and also considering our experience in this field, we present herein a review concerning the molecules obtained by the conjugation of peptides (amino acids) to small molecules (heterocycles as well as bioactive compounds). More than 125 examples of the conjugates citing nearly 100 references published during the period 2000 to 2022 having therapeutic applications in curing infectious diseases have been covered.
基于肽的药物在现代药物研发中正获得巨大的发展势头,近年来美国食品药品监督管理局(FDA)批准新药就是明证。另一方面,在过去几十年里,基于小分子的药物一直是药物研发不可或缺的一部分。含肽药物处于小分子药物和生物制剂之间。尽管肽类和小分子(主要是杂环化合物)在治愈许多疾病方面取得了成功,但作为治疗药物,它们都存在一些缺点。利用所谓的“共轭化学”可能会弥补这一差距,在共轭化学中,两个分子通过稳定的化学键相互连接,结果发现形成的共轭物具有吸引人的优势,从而消除了与单个分子相关的缺陷。在过去几十年里,分子杂交领域应运而生,为我们提供了新的高效分子结构,这些结构在药物化学中显示出了巨大的潜力。利用这一点,并结合我们在该领域的经验,我们在此对通过肽(氨基酸)与小分子(杂环化合物以及生物活性化合物)共轭得到的分子进行综述。文中涵盖了2000年至2022年期间发表文献中引用的125多个具有治疗传染病应用的共轭物实例,涉及近100篇参考文献。