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10.1016/j.ejmech.2020.113014

http://scihub22266oqcxt.onion/10.1016/j.ejmech.2020.113014
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suck abstract from ncbi


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pmid33218683      Eur+J+Med+Chem 2021 ; 211 (ä): 113014
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  • Dispirotripiperazine-core compounds, their biological activity with a focus on broad antiviral property, and perspectives in drug design (mini-review) #MMPMID33218683
  • Egorova A; Bogner E; Novoselova E; Zorn KM; Ekins S; Makarov V
  • Eur J Med Chem 2021[Feb]; 211 (ä): 113014 PMID33218683show ga
  • Viruses are obligate intracellular parasites and have evolved to enter the host cell. To gain access they come into contact with the host cell through an initial adhesion, and some viruses from different genus may use heparan sulfate proteoglycans for it. The successful inhibition of this early event of the infection by synthetic molecules has always been an attractive target for medicinal chemists. Numerous reports have yielded insights into the function of compounds based on the dispirotripiperazine scaffold. Analysis suggests that this is a structural requirement for inhibiting the interactions between viruses and cell-surface heparan sulfate proteoglycans, thus preventing virus entry and replication. This review summarizes our current knowledge about the early history of development, synthesis, structure-activity relationships and antiviral evaluation of dispirotripiperazine-based compounds and where they are going in the future.
  • |*Drug Design[MESH]
  • |Antiviral Agents/chemistry/*pharmacology[MESH]
  • |Heparan Sulfate Proteoglycans/antagonists & inhibitors/metabolism[MESH]
  • |Molecular Structure[MESH]
  • |Piperazines/chemistry/*pharmacology[MESH]
  • |Spiro Compounds/chemistry/*pharmacology[MESH]


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