化学
环肽
信使核糖核酸
药物发现
克拉斯
侧链
药代动力学
计算生物学
细胞内
吸收(声学)
生物化学
肽
药理学
基因
突变
生物
物理
有机化学
声学
聚合物
作者
Mirai Kage,Ryuji Hayashi,Atsushi Matsuo,Minoru Tamiya,Shino Kuramoto,Kazuhiro Ohara,Machiko Irie,Aya Chiyoda,Koji Takano,Toshiya Ito,Tomoya Kotake,Ryuuichi Takeyama,Shiho Ishikawa,Kenichi Nomura,Noriyuki Furuichi,Yuya Morita,Satoshi Hashimoto,Hatsuo Kawada,Yoshikazu Nishimura,Keiji Nii
标识
DOI:10.1016/j.bmc.2024.117830
摘要
Cyclic peptides are attracting attention as therapeutic agents due to their potential for oral absorption and easy access to tough intracellular targets. LUNA18, a clinical KRAS inhibitor, was transformed-without scaffold hopping-from the initial hit by using an mRNA display library that met our criteria for drug-likeness. In drug discovery using mRNA display libraries, hit compounds always possess a site linked to an mRNA tag. Here, we describe our examination of the Structure-Activity Relationship (SAR) using X-ray structures for chemical optimization near the site linked to the mRNA tag, equivalent to the C-terminus. Structural modifications near the C-terminus demonstrated a relatively wide range of tolerance for side chains. Furthermore, we show that a single atom modification is enough to change the pharmacokinetic (PK) profile. Since there are four positions where side chain modification is permissible in terms of activity, it is possible to flexibly adjust the pharmacokinetic profile by structurally optimizing the side chain. The side chain transformation findings demonstrated here may be generally applicable to hits obtained from mRNA display libraries.
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