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Journal of Medicinal Chemistry|April 7, 2011
Exploring the size limit of templates for inhibitors of the M2 ion channel of influenza A virusMaría D Duque, Chunlong Ma, Eva Torres, et al.
Bioorganic & Medicinal Chemistry|October 29, 2008
Synthesis and pharmacological evaluation of several ring-contracted amantadine analogsPelayo Camps, María D Duque, Santiago Vázquez, et al.
Molecules (Basel, Switzerland)|March 13, 2015
Multigram synthesis and in vivo efficacy studies of a novel multitarget anti-Alzheimer's compoundIrene Sola, Elisabet Viayna, Tània Gómez, et al.
Journal of Medicinal Chemistry|June 4, 2008
Novel donepezil-based inhibitors of acetyl- and butyrylcholinesterase and acetylcholinesterase-induced beta-amyloid aggregationPelayo Camps, Xavier Formosa, Carles Galdeano, et al.
Chemico-Biological Interactions|February 20, 2010
Tacrine-based dual binding site acetylcholinesterase inhibitors as potential disease-modifying anti-Alzheimer drug candidatesPelayo Camps, Xavier Formosa, Carles Galdeano, et al.
Journal of Medicinal Chemistry|August 12, 2009
Pyrano[3,2-c]quinoline-6-chlorotacrine hybrids as a novel family of acetylcholinesterase- and beta-amyloid-directed anti-Alzheimer compoundsPelayo Camps, Xavier Formosa, Carles Galdeano, et al.
Journal of Medicinal Chemistry|December 22, 2011
Huprine-tacrine heterodimers as anti-amyloidogenic compounds of potential interest against Alzheimer's and prion diseasesCarles Galdeano, Elisabet Viayna, Irene Sola, et al.
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