Bansal Nisha, Kathuria Deepika, Babu Arockia M, Dhiman Sonia, Lakhanpal Sorabh, Prasad K Nagendra, Kumar Roshan, Tyagi Yogita, Kumar Bhupinder, Singh Mahendra Pratap, Gaidhane Abhay M
Gramothan Vidyapeeth Home Science Girls PG College Sangaria Rajasthan India.
University Centre for Research and Development, Chandigarh University Gharuan 140413 Punjab India.
RSC Med Chem. 2025 Jan 21. doi: 10.1039/d4md00720d.
Renin-angiotensin-aldosterone system (RAAS) is crucial in cardiovascular homeostasis. Any disruption in this homeostasis often leads to numerous cardiovascular diseases (CVDs) and non-cardiovascular diseases. Small molecules that show ability toward mechanically modulating RAAS components have been developed to address this problem, thus providing opportunities for innovative drug discovery and development. This review is put forth to provide a comprehensive understanding not only on the signaling mechanisms of RAAS that lead to cardiovascular events but also on the use of small molecules targeting the modulation of RAAS components. Further, the detailed descriptions of the drugs affecting the RAAS and their pharmacodynamics, kinetics, and metabolism profiles are provided. This article also covers the limitations of the present therapeutic armory, followed by their mechanistic insights. A brief discussion is offered on the analysis of the chemical space parameters of the drugs affecting RAAS compared to other cardiovascular and renal categories of medications approved by the US FDA. This review provides structural insights and emphasizes the importance of integrating the current therapeutic regimen with pharmacological tactics to accelerate the development of new therapeutics targeting the RAAS components for improved and efficacious cardiovascular outcomes. Finally, chemical spacing parameters of RAAS modulators are provided, which will help in understanding their peculiarities in modulating the RAAS signaling through structural and functional analyses. Furthermore, this review will assist medicinal chemists working in this field in developing better drug regimens with improved selectivity and efficacy.
肾素-血管紧张素-醛固酮系统(RAAS)在心血管稳态中至关重要。这种稳态的任何破坏通常都会导致多种心血管疾病(CVD)和非心血管疾病。已开发出能够机械调节RAAS组分的小分子来解决这一问题,从而为创新药物的发现和开发提供了机会。本综述旨在不仅全面了解导致心血管事件的RAAS信号传导机制,还全面了解靶向调节RAAS组分的小分子的应用。此外,还提供了影响RAAS的药物及其药效学、动力学和代谢概况的详细描述。本文还涵盖了当前治疗手段的局限性及其机制见解。与美国食品药品监督管理局(FDA)批准的其他心血管和肾脏类药物相比,对影响RAAS的药物的化学空间参数分析进行了简要讨论。本综述提供了结构见解,并强调了将当前治疗方案与药理学策略相结合以加速开发针对RAAS组分的新疗法以改善心血管结局并提高疗效的重要性。最后,提供了RAAS调节剂的化学空间参数,这将有助于通过结构和功能分析了解它们在调节RAAS信号传导方面的特性。此外,本综述将帮助该领域的药物化学家开发具有更高选择性和疗效的更好药物方案。