作者的详细信息

Makhaeva, G.

栏目 标题 文件
卷 65, 编号 2 (2016) Full Articles Molecular design of N,N-disubstituted 2-aminothiazolines as selective carboxylesterase inhibitors
卷 65, 编号 5 (2016) Full Articles Synthesis and studies of biological activity of N-(4-tert-butylbenzyl)-N-(pyridin-3-ylmethyl)-2-aminothiazolines as potential multifunctional agents for treatment of neurodegenerative diseases
卷 65, 编号 6 (2016) Full Articles 1,2,4-Thiadiazoles as promising multifunctional agents for treatment of neurodegenerative diseases
卷 65, 编号 6 (2016) Full Articles Molecular polymorphism of human enzymes as the basis of individual sensitivity to drugs. Supercomputer-assisted modeling as a tool for analysis of structural changes and enzymatic activity of proteins
卷 65, 编号 11 (2016) Full Articles Synthesis of γ-carbolines containing NO-donor fragment and assessment of their anticholinesterase activity
卷 66, 编号 7 (2017) Full Articles 1,2,4-Thiadiazole derivatives as effective NMDA receptor blockers with anticholinesterase activity and antioxidant properties
卷 66, 编号 10 (2017) Reviews Targeted synthesis and biological activity of polypharmacophoric agents for the treatment of neurodegenerative diseases
卷 66, 编号 10 (2017) Full Articles Synthesis of new N-(pyridin-3-ylmethyl)-2-aminothiazoline derivatives possessing anticholinesterase and antiradical activity as potential multifunctional agents for the treatment of neurodegenerative diseases
卷 67, 编号 9 (2018) Article Influence of the γ-carboline and carbazole pharmacophore moieties on anticholinesterase and antiradical activity of multifunctional agents for the treatment of neurodegenerative diseases
卷 67, 编号 11 (2018) Full Articles Synthesis and biological activity of 5-vinyl- and 5-allyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoles
卷 67, 编号 11 (2018) Full Articles Aminoadamantane conjugates with carbazole derivatives as potential multitarget agents for the treatment of Alzheimer’s disease. Effect of the spacer structure
卷 68, 编号 5 (2019) Review Cholinesterase and carboxylesterase inhibitors as pharmacological agents
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