A new photoisomer of the promising “anti-Alzheimer” drug candidate (±) huperzine A is described. The new substance was formed via a photoisomerization reaction and was found to be 1-amino-13-ethylidene-11-methyl-6-aza-tetracyclo-[7.3.1.02.7.04.7]-trideca-2,10-diene-5-one using NMR analysis. The kinetics of its formation was studied and proven to be of first-order. The described photoisomer showed a significant loss in activity, being more than 100 times less active than (−) huperzine A itself. The new substance was named photohuperzine A, referring to its photopyridone substructure
Huperzine A is a bioactive compound derived from traditional Chinese medicine plant Qian Ceng Ta (Hu...
Antibiotic resistance continues to be an ominous threat facing human health globally and urgent acti...
Huperzine A (HUP), a natural, potent, ‘slow, ’ reversible inhibitor of antiacetylcholinesterase (ACh...
A new photoisomer of the promising " anti-Alzheimer" drug candidate (±) huperzine A is described. Th...
Photocyclization of aryl vinyl ethers reportedly proceeds via carbonyl ylide intermediates. Previous...
The primary goal of this project is to explore the synthesis of huperzine alkaloids via the photoini...
In one synthetic route toward analogs of Huperzine, a natural potent reversible inhibitor of acetylc...
The natural product huperzine A has been found to possess activity as a nootropic agent. Because of ...
Huperzine A is an alkaloid isolated from Huperzia serrata (Thunb.) Trev., a Chinese club moss the ex...
Abstract: Recent studies have proved that huperzine A (HupA) possesses different pharma-cological ac...
This paper describes our preliminary results on the ADMET, synthesis, biochemical evaluation, and mo...
This paper describes our preliminary results on the ADMET, synthesis, biochemical evaluation, and mo...
Huperzine A, a potential agent for therapy in Alzheimer’s disease and for prophylaxis of organophosp...
The dissociation of huperzine A (hupA) from Torpedo californica acetylcholinesterase (TcAChE) was in...
Huperzine A is a selective and potent reversible acetylcholinesterase (AChE) inhibitor isolated from...
Huperzine A is a bioactive compound derived from traditional Chinese medicine plant Qian Ceng Ta (Hu...
Antibiotic resistance continues to be an ominous threat facing human health globally and urgent acti...
Huperzine A (HUP), a natural, potent, ‘slow, ’ reversible inhibitor of antiacetylcholinesterase (ACh...
A new photoisomer of the promising " anti-Alzheimer" drug candidate (±) huperzine A is described. Th...
Photocyclization of aryl vinyl ethers reportedly proceeds via carbonyl ylide intermediates. Previous...
The primary goal of this project is to explore the synthesis of huperzine alkaloids via the photoini...
In one synthetic route toward analogs of Huperzine, a natural potent reversible inhibitor of acetylc...
The natural product huperzine A has been found to possess activity as a nootropic agent. Because of ...
Huperzine A is an alkaloid isolated from Huperzia serrata (Thunb.) Trev., a Chinese club moss the ex...
Abstract: Recent studies have proved that huperzine A (HupA) possesses different pharma-cological ac...
This paper describes our preliminary results on the ADMET, synthesis, biochemical evaluation, and mo...
This paper describes our preliminary results on the ADMET, synthesis, biochemical evaluation, and mo...
Huperzine A, a potential agent for therapy in Alzheimer’s disease and for prophylaxis of organophosp...
The dissociation of huperzine A (hupA) from Torpedo californica acetylcholinesterase (TcAChE) was in...
Huperzine A is a selective and potent reversible acetylcholinesterase (AChE) inhibitor isolated from...
Huperzine A is a bioactive compound derived from traditional Chinese medicine plant Qian Ceng Ta (Hu...
Antibiotic resistance continues to be an ominous threat facing human health globally and urgent acti...
Huperzine A (HUP), a natural, potent, ‘slow, ’ reversible inhibitor of antiacetylcholinesterase (ACh...