化学
醛
减肥
群(周期表)
肥胖
组合化学
立体化学
药理学
有机化学
内科学
催化作用
医学
作者
Zhi Jiang,Yu‐Tao Hu,Shi‐Yao Guo,Yi‐Xian Li,Dandan Zhao,Liyuan Wei,Yu-Wei Lin,Shumin Xu,Shi‐Liang Huang,Qingjiang Li,Jia‐Heng Tan,Yong Rao,Shuo‐Bin Chen,Zhi‐Shu Huang
标识
DOI:10.1021/acs.jmedchem.4c01242
摘要
The discovery of effective and safe antiobesity agents remains a challenging yet promising field. Our previous studies identified Bouchardatine derivatives as potential antiobesity agents. However, the 8a-aldehyde moiety rendered them unsuitable for drug development. In this study, we designed two series of novel derivatives to modify this structural feature. Through a structure-activity relationship study, we elucidated the role of the 8a-aldehyde group in toxicity induction. We identified compound 14d, featuring an 8a-N-acylhydrazone moiety, which exhibited significant lipid-lowering activity and reduced toxicity. Compound 14d shares a similar lipid-lowering mechanism with our lead compound 3, but demonstrates improved pharmacokinetic properties and safety profile. Both oral and injectable administration of 14d significantly reduced body weight gain and ameliorated metabolic syndrome in diet-induced obese mice. Our findings identify 14d as a promising antiobesity agent and highlight the potential of substituting the aldehyde group with an N-acylhydrazone to enhance drug-like properties.
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