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8篇 您的检索式：作者名="Formosa X"

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		题名	作者	年代	出处	被引量
	1	Synthesis and pharmacological evaluation of huprine-tacrine heterodimers: subnanomolar dual binding site acetylcholinesterase inhibitors 显示文摘	Camps P Formosa X Munoz-Torrero D	2005	J Med Chem2005，48，6：	1
	2	Novel donepezil- based inhibitors of acetyl- and butyrylcholinesterase and acetylcholinesterase-induced beta-amyloid aggregation显示文摘	Camps P Formosa X Galdeano C	2008	J Med Chem2008，51，12：	1
	3	Pyrano[3,2-c]quinoline-6-chlorotacrine hybrids as a novel family of acetylcholinesterase-and beta-amyloid-directed anti-Alzheimer compounds显示文摘	Camps P Formosa X Galdeano C		0，，：	1
	4	Pyrano : hybrids as a novel family β-amyloid-directed anti- J Med Chem, 2009, 52 of acetylcholinesterase and alzheimer compounds 显示文摘	Camps P Formosa X Galdeano C	2009	(17) :5367 -53792009，，17：	1
	5	Tacrine- based dual binding site acetyleholinesterase inhibitors as potential disease-modifying anti-alzheimer drug candidates 显示文摘	Camps P Formosa X Galdeano C	2010	Chemieo-Biological Interactions2010，187，：	1
	6	Pyranoquinoline-6-Chlorotacrine Hybrids as a Novel Family of Acetylcho-linesterase-and beta-Amyloid-Directed Anti-Alzheimer Compounds显示文摘	Camps P Formosa X Galdeano C	2009	J Med Chem2009，52，17：	1
	7	Gene knockout using transcription activator-like effeetor nucleases (TALENs) reveals that human NDUFA9 protein is essential for stabilizing the junction between membrane and matrix arms of complex I 显示文摘	Strond D A Formosa L E Wijeyeratne X W	2013	J Biol Chem2013，288，3：	1
	8	Synthesis and pharmacological evaluation of huprine-tacrine heterodimers: subnanomolar dual binding site acetylcholinesterase 显示文摘	Camps P Formosa X Diego MT	2005	J Med Chem2005，48，：	1

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