tetano
Editor, Senior Moderator
Molecules. 2019 Mar 6;24(5). pii: E921. doi: 10.3390/molecules24050921.
[h=1]Evolution and Biological Evaluation of Matrinic Derivatives with Amantadine Fragments As New Anti-Influenza Virus Agents.[/h] Niu T[SUP]1[/SUP], Zhao X[SUP]2[/SUP], Jiang J[SUP]3[/SUP], Yan H[SUP]4[/SUP], Li Y[SUP]5[/SUP], Tang S[SUP]6[/SUP], Li Y[SUP]7[/SUP], Song D[SUP]8[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] A series of novel tricyclic matrinic derivatives with 11-adamantyl substitution were designed, synthesized, and evaluated for their activities against Influenza A H3N2 virus, based on the privileged structure strategy. Structure-activity relationship (SAR) analysis indicated that the introduction of an 11-adamantyl might be helpful for the potency. Among them, compounds 9f and 9j exhibited the promising anti-H3N2 activities with IC[SUB]50[/SUB] values of 7.2 μM and 10.2 μM, respectively, better than that of lead 1. Their activities were further confirmed at the protein level. Moreover, compound 9f displayed a high pharmacokinetic (PK) stability profile in whole blood and a safety profile in vivo. In primary mechanism, compound 9f could inhibit the virus replication cycle at early stage by targeting M2 protein, consistent with that of the parent amantadine. This study provided powerful information for further strategic optimization to develop these compounds into a new class of anti-influenza agents.
[h=4]KEYWORDS:[/h] H3N2; anti-virus; influenza A virus; structure?activity relationship; tricyclic matrinic derivatives
PMID: 30845734 DOI: 10.3390/molecules24050921
[h=1]Evolution and Biological Evaluation of Matrinic Derivatives with Amantadine Fragments As New Anti-Influenza Virus Agents.[/h] Niu T[SUP]1[/SUP], Zhao X[SUP]2[/SUP], Jiang J[SUP]3[/SUP], Yan H[SUP]4[/SUP], Li Y[SUP]5[/SUP], Tang S[SUP]6[/SUP], Li Y[SUP]7[/SUP], Song D[SUP]8[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] A series of novel tricyclic matrinic derivatives with 11-adamantyl substitution were designed, synthesized, and evaluated for their activities against Influenza A H3N2 virus, based on the privileged structure strategy. Structure-activity relationship (SAR) analysis indicated that the introduction of an 11-adamantyl might be helpful for the potency. Among them, compounds 9f and 9j exhibited the promising anti-H3N2 activities with IC[SUB]50[/SUB] values of 7.2 μM and 10.2 μM, respectively, better than that of lead 1. Their activities were further confirmed at the protein level. Moreover, compound 9f displayed a high pharmacokinetic (PK) stability profile in whole blood and a safety profile in vivo. In primary mechanism, compound 9f could inhibit the virus replication cycle at early stage by targeting M2 protein, consistent with that of the parent amantadine. This study provided powerful information for further strategic optimization to develop these compounds into a new class of anti-influenza agents.
[h=4]KEYWORDS:[/h] H3N2; anti-virus; influenza A virus; structure?activity relationship; tricyclic matrinic derivatives
PMID: 30845734 DOI: 10.3390/molecules24050921