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Synthesis and pharmacological evaluation of donepezil-based agents as new cholinesterase/monoamine oxidase inhibitors for the potential application against Alzheimer's disease.
Li, Fan; Wang, Zhi-Min; Wu, Jia-Jia; Wang, Jin; Xie, Sai-Sai; Lan, Jin-Shuai; Xu, Wei; Kong, Ling-Yi; Wang, Xiao-Bing.
Afiliação
  • Li F; a State Key Laboratory of Natural Medicines, Department of Natural Medicinal Chemistry, China Pharmaceutical University , People's Republic of China.
  • Wang ZM; a State Key Laboratory of Natural Medicines, Department of Natural Medicinal Chemistry, China Pharmaceutical University , People's Republic of China.
  • Wu JJ; a State Key Laboratory of Natural Medicines, Department of Natural Medicinal Chemistry, China Pharmaceutical University , People's Republic of China.
  • Wang J; a State Key Laboratory of Natural Medicines, Department of Natural Medicinal Chemistry, China Pharmaceutical University , People's Republic of China.
  • Xie SS; a State Key Laboratory of Natural Medicines, Department of Natural Medicinal Chemistry, China Pharmaceutical University , People's Republic of China.
  • Lan JS; a State Key Laboratory of Natural Medicines, Department of Natural Medicinal Chemistry, China Pharmaceutical University , People's Republic of China.
  • Xu W; a State Key Laboratory of Natural Medicines, Department of Natural Medicinal Chemistry, China Pharmaceutical University , People's Republic of China.
  • Kong LY; a State Key Laboratory of Natural Medicines, Department of Natural Medicinal Chemistry, China Pharmaceutical University , People's Republic of China.
  • Wang XB; a State Key Laboratory of Natural Medicines, Department of Natural Medicinal Chemistry, China Pharmaceutical University , People's Republic of China.
J Enzyme Inhib Med Chem ; 31(sup3): 41-53, 2016.
Article em En | MEDLINE | ID: mdl-27384289
In a continuing effort to develop multitargeted compounds as potential treatment agents against Alzheimer's disease (AD), a series of donepezil-like compounds were designed, synthesized and evaluated. In vitro studies showed that most of the designed compounds displayed potent inhibitory activities toward AChE, BuChE, MAO-B and MAO-A. Among them, w18 was a promising agent with balanced activities, which exhibited a moderate cholinesterase inhibition (IC50, 0.220 µM for eeAChE; 1.23 µM for eqBuChE; 0.454 µM for hAChE) and an acceptable inhibitory activity against monoamine oxidases (IC50, 3.14 µM for MAO-B; 13.4 µM for MAO-A). Moreover, w18 could also be a metal-chelator, and able to cross the blood-brain barrier with low cell toxicity on PC12 cells. Taken together, these results suggested that w18 might be a promising multitargeted compound for AD treatment.
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Base de dados: MEDLINE Assunto principal: Piperidinas / Inibidores da Colinesterase / Doença de Alzheimer / Indanos / Inibidores da Monoaminoxidase Idioma: En Ano de publicação: 2016 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Piperidinas / Inibidores da Colinesterase / Doença de Alzheimer / Indanos / Inibidores da Monoaminoxidase Idioma: En Ano de publicação: 2016 Tipo de documento: Article