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Advances toward multifunctional cholinesterase and ß-amyloid aggregation inhibitors.
Panek, Dawid; Wichur, Tomasz; Godyn, Justyna; Pasieka, Anna; Malawska, Barbara.
Afiliación
  • Panek D; Department of Physicochemical Drug Analysis, Chair of Pharmaceutical Chemistry, Faculty of Pharmacy, Jagiellonian University Medical College, 30-688 Kraków, Medyczna 9, Poland.
  • Wichur T; Department of Physicochemical Drug Analysis, Chair of Pharmaceutical Chemistry, Faculty of Pharmacy, Jagiellonian University Medical College, 30-688 Kraków, Medyczna 9, Poland.
  • Godyn J; Department of Physicochemical Drug Analysis, Chair of Pharmaceutical Chemistry, Faculty of Pharmacy, Jagiellonian University Medical College, 30-688 Kraków, Medyczna 9, Poland.
  • Pasieka A; Department of Physicochemical Drug Analysis, Chair of Pharmaceutical Chemistry, Faculty of Pharmacy, Jagiellonian University Medical College, 30-688 Kraków, Medyczna 9, Poland.
  • Malawska B; Department of Physicochemical Drug Analysis, Chair of Pharmaceutical Chemistry, Faculty of Pharmacy, Jagiellonian University Medical College, 30-688 Kraków, Medyczna 9, Poland.
Future Med Chem ; 9(15): 1835-1854, 2017 10.
Article en En | MEDLINE | ID: mdl-28925729
ABSTRACT
The emergence of a multitarget design approach in the development of new potential anti-Alzheimer's disease agents has resulted in the discovery of many multifunctional compounds focusing on various targets. Among them the largest group comprises inhibitors of both cholinesterases, with additional anti-ß-amyloid aggregation activity. This review describes recent advances in this research area and presents the most interesting compounds reported over a 2-year span (2015-2016). The majority of hybrids possess heterodimeric structures obtained by linking structurally active fragments interacting with different targets. Multipotent cholinesterase inhibitors with ß-amyloid antiaggregating activity may additionally possess antioxidative, neuroprotective or metal-chelating properties or less common features such as anti-ß-secretase or τ-antiaggregation activity.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Colinesterasas / Péptidos beta-Amiloides Límite: Humans Idioma: En Revista: Future Med Chem Año: 2017 Tipo del documento: Article País de afiliación: Polonia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Colinesterasas / Péptidos beta-Amiloides Límite: Humans Idioma: En Revista: Future Med Chem Año: 2017 Tipo del documento: Article País de afiliación: Polonia
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