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Tacrine:MCnc:Pt:Ser/Plas:Qn

Known as: Tacrina:Concentración de masa:Punto temporal:Suero o Plasma:Qn, Takrin:KütlKons:Zml?:Ser/Plaz:Kant, ???:????:????:??/??:?? 
 
National Institutes of Health

Papers overview

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2015
2015
A new series of tacrine-based acetylcholinesterase (AChE) inhibitors 7a-l were designed by replacing the benzene ring of tacrine… Expand
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Highly Cited
2014
Highly Cited
2014
New tacrine-carbazole hybrids were developed as potential multifunctional anti-Alzheimer agents for their cholinesterase… Expand
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2014
2014
A series of multifunctional directed 3-arylcoumarin-tetracyclic tacrine derivatives was designed and synthesized for the… Expand
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Highly Cited
2012
Highly Cited
2012
A family of huprine-tacrine heterodimers has been developed to simultaneously block the active and peripheral sites of… Expand
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2012
2012
Cooperating mercapto groups with tacrine in a single molecular, novel multifunctional compounds have been designed and… Expand
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2011
2011
A new series of heterobivalent tacrine derivatives were designed, synthesized and evaluated as potential multi-functional anti… Expand
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Highly Cited
2006
Highly Cited
2006
Two series of novel heterobivalent tacrine derivatives were synthesized. A trimethoxy substituted benzene was linked to the… Expand
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Highly Cited
2005
Highly Cited
2005
A series of huprine-tacrine heterodimers has been developed by connection of huprine Y, a compound with one of the highest… Expand
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Highly Cited
2002
Highly Cited
2002
In the search for highly selective and potent derivatives of tacrine (1a), a number of homodimeric tacrine congeners were… Expand
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1995
1995
1. Tacrine (1,2,3,4-tetrahydro-9-aminoacridine) which is used in Alzheimer's disease, causes elevation of liver transaminases… Expand
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