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Discovery of Cinnamic Acid Derivatives as Potent Anti- H. pylori Agents.
- Source :
-
Molecules (Basel, Switzerland) [Molecules] 2024 Sep 25; Vol. 29 (19). Date of Electronic Publication: 2024 Sep 25. - Publication Year :
- 2024
-
Abstract
- Antibiotics are currently used for the treatment of Helicobacter pylori ( H. pylori ), which is confirmed to be the major cause of gastric disorders. However, the long-term consumption of antibiotics has already caused antibiotic resistance and side effects in vivo. Therefore, there is an emerging need for searching for safe and effective anti- H. pylori agents. Inspired by the excellent bioactivities of cinnamic acid, a series of cinnamic acid derivatives (compounds 1 - 30 ) were synthesized and determined for H. pylori inhibition. The initial screening revealed that compound 23 , a 2,4-dinitro cinnamic acid derivative containing 4-methoxyphenol, showed excellent H. pylori inhibition with an MIC value of 4 μM. Further studies indicated that compound 23 showed anti-bacterial activity and had a bactericidal effect on H. pylori due to the destruction of the bacterial structure. Molecular docking analysis revealed that the 2,4-dinitro groups in cinnamic acid moiety formed hydrogen bonding with amino acid residues in an active pocket of H. pylori protein. Interestingly, the ester moiety fitted into the hydrophobic pocket, attaining additional stability to compound 23 . Above all, the present study reveals that compound 23 could be considered a promising anti- H. pylori agent to treat H. pylori causing gastritis.
- Subjects :
- Structure-Activity Relationship
Molecular Structure
Helicobacter Infections drug therapy
Helicobacter Infections microbiology
Humans
Helicobacter pylori drug effects
Cinnamates chemistry
Cinnamates pharmacology
Cinnamates chemical synthesis
Anti-Bacterial Agents pharmacology
Anti-Bacterial Agents chemistry
Anti-Bacterial Agents chemical synthesis
Molecular Docking Simulation
Microbial Sensitivity Tests
Subjects
Details
- Language :
- English
- ISSN :
- 1420-3049
- Volume :
- 29
- Issue :
- 19
- Database :
- MEDLINE
- Journal :
- Molecules (Basel, Switzerland)
- Publication Type :
- Academic Journal
- Accession number :
- 39407478
- Full Text :
- https://doi.org/10.3390/molecules29194548