Master's thesis in biological chemistryThis project presents the synthesis of tacrine and coumarin scaffolds armed with an alkyl-chain of varying length with an azido functionality and isocryptolepine scaffold armed with a terminal alkyne. The synthesis of these compounds lead to the successful synthesis of the potential dual binding site acetylcholinesterase inhibitors, a tacrine-cryptolepine hybrid with a 3 carbon-linker and a coumarin-isocryptolepine hybrid with a 4 carbon-linker assembled via copper-catalyzed azidealkyne cycloaddition (CuAAC). The attempted synthesis of the same hybrids with different linker-length (6 and 8) were not successful.submittedVersio
A novel series of tacrine derivatives were designed and synthesized by combining caffeic acid (CA), ...
We describe herein the development of novel huperzine A-tacrine hybrids characterized by 3-methylbic...
Title: Synthesis and in vitro evaluation of pyridinium type acetylcholinesterase inhibitors Author: ...
This project presents the synthesis of tacrine and coumarin scaffolds armed with an alkyl-chain of v...
A novel series of tacrine-lophine hybrids was synthesized and tested for their ability to inhibit ac...
A series of novel tacrine derivatives and tacrine–coumarin heterodimers were designed, synthesized, ...
AbstractBackground: Methods for the rapid and efficient preparation of drug candidates through combi...
To further investigate the M1 muscarinic acetylcholine receptor subtype and to explore new, putative...
Hybrid acetylcholinesterase inhibitors composed of a key fragment of huperzine A and an intact tacri...
The synthesis of highly potent and selective acetylcholinesterase inhibitors, tacrine analogues with...
Both cholinesterases (AChE and BChE) and kinases, such as GSK-3α/β, are associated with the patholog...
<p>The cholinergic hypothesis has long been a “polar star” in drug discovery for Alzheimer’s disease...
Acetylcholinesterase inhibitors (AChEIs) are currently the drugs of choice, although only symptomati...
A marine natural product, pulmonarin B (1), and a series of related tacrine hybrid analogues were sy...
A novel series of tacrine derivatives were designed and synthesized by combining caffeic acid (CA), ...
We describe herein the development of novel huperzine A-tacrine hybrids characterized by 3-methylbic...
Title: Synthesis and in vitro evaluation of pyridinium type acetylcholinesterase inhibitors Author: ...
This project presents the synthesis of tacrine and coumarin scaffolds armed with an alkyl-chain of v...
A novel series of tacrine-lophine hybrids was synthesized and tested for their ability to inhibit ac...
A series of novel tacrine derivatives and tacrine–coumarin heterodimers were designed, synthesized, ...
AbstractBackground: Methods for the rapid and efficient preparation of drug candidates through combi...
To further investigate the M1 muscarinic acetylcholine receptor subtype and to explore new, putative...
Hybrid acetylcholinesterase inhibitors composed of a key fragment of huperzine A and an intact tacri...
The synthesis of highly potent and selective acetylcholinesterase inhibitors, tacrine analogues with...
Both cholinesterases (AChE and BChE) and kinases, such as GSK-3α/β, are associated with the patholog...
<p>The cholinergic hypothesis has long been a “polar star” in drug discovery for Alzheimer’s disease...
Acetylcholinesterase inhibitors (AChEIs) are currently the drugs of choice, although only symptomati...
A marine natural product, pulmonarin B (1), and a series of related tacrine hybrid analogues were sy...
A novel series of tacrine derivatives were designed and synthesized by combining caffeic acid (CA), ...
We describe herein the development of novel huperzine A-tacrine hybrids characterized by 3-methylbic...
Title: Synthesis and in vitro evaluation of pyridinium type acetylcholinesterase inhibitors Author: ...