Issue 17, 2008

Design and synthesis of bioactive 1,2-annulated adamantane derivatives

Abstract

Adamantanopyrrolidines 8, 9 and 10, adamantanopyrrolidines 16 and 18, adamantanoxazolone 20, adamantanopyrazolone 23, adamantanopyrazolothione 24 and adamantanocyclopentanamine 32 were synthesized and tested for anti-influenza A virus and trypanocidal activity. The stereoelectronic requirements for optimal antiviral and trypanocidal potency were investigated. Pyrrolidine 16 proved to be the most active of the compounds tested against influenza A virus, being 4-fold more active than amantadine, equipotent to rimantadine and 19-fold more potent than ribavirin. Oxazolone 20 showed significant trypanocidal activity against bloodstream forms of the African trypanosome, Trypanosoma brucei, being approximately 3 times more potent than rimantadine and almost 50-fold more active than amantadine.

Graphical abstract: Design and synthesis of bioactive 1,2-annulated adamantane derivatives

Article information

Article type
Paper
Submitted
25 Mar 2008
Accepted
06 Jun 2008
First published
09 Jul 2008

Org. Biomol. Chem., 2008,6, 3177-3185

Design and synthesis of bioactive 1,2-annulated adamantane derivatives

G. Zoidis, A. Tsotinis, N. Kolocouris, J. M. Kelly, S. R. Prathalingam, L. Naesens and E. De Clercq, Org. Biomol. Chem., 2008, 6, 3177 DOI: 10.1039/B804907F

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