Choi Yujeong, Kim Younghyun, Boo Hye Joon, Yoon Danbi, Cha Jeong Seok, Yoo Jiho
College of Pharmacy, Chung-Ang University, Seoul 06974, Republic of Korea.
Research Institute of Pharmacy, Chung-Ang University, Seoul 06974, Republic of Korea.
Biomolecules. 2025 Sep 10;15(9):1303. doi: 10.3390/biom15091303.
Natural product-derived drugs represent a cornerstone of modern pharmacotherapy, with many serving as essential therapeutic agents across diverse medical conditions. Recent advances in structural biology have provided unprecedented insights into the molecular mechanisms underlying their biological activities. This review presents a comprehensive structural analysis of five representative natural product-derived drugs: digoxin, simvastatin, morphine, paclitaxel, and penicillin. Through an examination of high-resolution crystal structures and cryo-electron microscopy (cryo-EM) data, we elucidate how these compounds interact with their respective protein targets and modulate biological functions. The structural data reveal diverse binding mechanisms-ranging from competitive inhibition and covalent modification to allosteric modulation via conformational selection and induced fit-demonstrating how natural products achieve their therapeutic effects through precise molecular recognition. These structural insights provide a molecular foundation for understanding natural product pharmacology and offer valuable guidance for structure-based drug design approaches in developing next-generation therapeutics.
天然产物衍生药物是现代药物治疗的基石,许多此类药物在多种医疗状况下都是重要的治疗药物。结构生物学的最新进展为其生物活性背后的分子机制提供了前所未有的见解。本综述对五种代表性的天然产物衍生药物进行了全面的结构分析:地高辛、辛伐他汀、吗啡、紫杉醇和青霉素。通过研究高分辨率晶体结构和冷冻电子显微镜(cryo-EM)数据,我们阐明了这些化合物如何与各自的蛋白质靶点相互作用并调节生物学功能。结构数据揭示了多种结合机制——从竞争性抑制、共价修饰到通过构象选择和诱导契合进行的变构调节——展示了天然产物如何通过精确的分子识别实现其治疗效果。这些结构见解为理解天然产物药理学提供了分子基础,并为基于结构的药物设计方法开发下一代治疗药物提供了有价值的指导。