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Chem Biol Drug Des ; 103(3): e14506, 2024 03.
Artigo em Inglês | MEDLINE | ID: mdl-38480508

RESUMO

A series of new betulin, lupeol, erythrodiol, and oleanolic acid phosphoryloxy- and furoyloxy-derivatives has been synthesized and their structure was confirmed by NMR spectroscopy. Synthesized compounds were subjected to Ellman's assays to determine their ability to inhibit the enzymes AChE and BChE. Among them, diethoxyphosphoryloxy-oleanolic acid inhibited BChE with a value of 99%, thereby acting as a mixed-type inhibitor holding very low Ki values of Ki = 6.59 nM and Ki ' = 1.97 nM, respectively.


Assuntos
Ácido Oleanólico , Triterpenos , Butirilcolinesterase/química , Inibidores da Colinesterase/farmacologia , Inibidores da Colinesterase/química , Acetilcolinesterase/metabolismo , Ácido Oleanólico/farmacologia , Triterpenos/farmacologia , Triterpenos/química , Relação Estrutura-Atividade
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