Bäckbro K
Publications:
| Title | Authors | Year | Journal |
|---|---|---|---|
| Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors. 3. Synthesis and further structure-activity relationship studies of PETT analogues. | Bäckbro K | 1999 | J Med Chem |
| Inhibition of human immunodeficiency virus type 1 wild-type and mutant reverse transcriptases by the phenyl ethyl thiazolyl thiourea derivatives trovirdine and MSC-127. | Bäckbro K | 1995 | Antiviral research |
| Human immunodeficiency virus type 1 (HIV-1) strains selected for resistance against the HIV-1-specific [2',5'-bis-O-(tert-butyldimethylsilyl)-3'-spiro- 5''-(4''-amino-1'',2''-oxathiole-2'',2''-dioxide)]-beta-D-pentofurano syl (TSAO) nucleoside analogues retain sensitivity to HIV-1-specific nonnucleoside inhibitors. | Bäckbro K | 1993 | Proceedings of the National Academy of Sciences of the United States of America |
Showing 1 to 3 of 3 entries