Abstract:
:A set of (-)-isopulegol derived octahydro-2H-chromen-4-ols was synthesized and evaluated in vitro for antiviral activity against panel of reference influenza virus strains differing in subtype, origin (human or avian) and drug resistance. Compound (4R)-11a produced via one-pot synthesis by interaction between (-)-isopulegol and acetone was found to exhibit an outstanding activity against a number of H1N1 and H2N2 influenza virus strains with selectivity index more than 1500. (4R)-11a was shown to be most potent at early stages of viral cycle. Good correlation between anti-viral activity and calculated binding energy to hemagglutinin TBHQ active site was demonstrated.
journal_name
Bioorg Med Chem Lettjournal_title
Bioorganic & medicinal chemistry lettersauthors
Ilyina IV,Zarubaev VV,Lavrentieva IN,Shtro AA,Esaulkova IL,Korchagina DV,Borisevich SS,Volcho KP,Salakhutdinov NFdoi
10.1016/j.bmcl.2018.04.057subject
Has Abstractpub_date
2018-06-15 00:00:00pages
2061-2067issue
11eissn
0960-894Xissn
1464-3405pii
S0960-894X(18)30369-Xjournal_volume
28pub_type
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