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Development of Novel N -Acylhydrazone Derivatives with High Anti-obesity Activity and Improved Safety by Exploring the Pharmaceutical Properties of Aldehyde Group.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2024 Jul 25; Vol. 67 (14), pp. 12439-12458. Date of Electronic Publication: 2024 Jul 12. - Publication Year :
- 2024
-
Abstract
- 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.
- Subjects :
- Animals
Mice
Structure-Activity Relationship
Male
Mice, Inbred C57BL
Diet, High-Fat adverse effects
Humans
Mice, Obese
Molecular Structure
Anti-Obesity Agents pharmacology
Anti-Obesity Agents chemical synthesis
Anti-Obesity Agents pharmacokinetics
Anti-Obesity Agents therapeutic use
Anti-Obesity Agents chemistry
Hydrazones pharmacology
Hydrazones chemistry
Hydrazones chemical synthesis
Hydrazones pharmacokinetics
Hydrazones therapeutic use
Aldehydes chemistry
Obesity drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4804
- Volume :
- 67
- Issue :
- 14
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 38996004
- Full Text :
- https://doi.org/10.1021/acs.jmedchem.4c01242