Synthesis of triterpenoid acylates: Effective reproduction inhibitors of influenza A (H1N1) and papilloma viruses
Identifieur interne : 002713 ( Main/Exploration ); précédent : 002712; suivant : 002714Synthesis of triterpenoid acylates: Effective reproduction inhibitors of influenza A (H1N1) and papilloma viruses
Auteurs : O. B. Kazakova [Russie] ; N. I. Medvedeva [Russie] ; I. P. Baikova [Russie] ; G. A. Tolstikov [Russie] ; T. V. Lopatina [Russie] ; M. S. Yunusov [Russie] ; L. Zaprutko [Pologne]Source :
- Russian Journal of Bioorganic Chemistry [ 1068-1620 ] ; 2010-11-01.
English descriptors
- KwdEn :
Abstract
Abstract: The synthesis of a new group of triterpenoid acylates has been conducted on the basis of oleanolic, glycyrrhetic, and ursolic acids and betulin. 28-ortho-Methoxycynnamoylbetulin has been demonstrated to possess high activity against the influenza type A (H1N1) virus with the selectivity index SI > 100 while studying the activity of the synthesized compounds in relation to the reproduction of viral pathogens of respiratory infections. The high activity of 3,28-dinicotinoylbetulin against the papilloma virus (strain HPV-11) was detected with the selectivity index SI 35.
Url:
DOI: 10.1134/S1068162010060142
Affiliations:
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<front><div type="abstract" xml:lang="en">Abstract: The synthesis of a new group of triterpenoid acylates has been conducted on the basis of oleanolic, glycyrrhetic, and ursolic acids and betulin. 28-ortho-Methoxycynnamoylbetulin has been demonstrated to possess high activity against the influenza type A (H1N1) virus with the selectivity index SI > 100 while studying the activity of the synthesized compounds in relation to the reproduction of viral pathogens of respiratory infections. The high activity of 3,28-dinicotinoylbetulin against the papilloma virus (strain HPV-11) was detected with the selectivity index SI 35.</div>
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