A successful strategy in the development of antiretroviral drugs has been the targetting of the virally encoded reverse transcriptase (RT) (De Clercq, 1998; Artico, 1996). Two classes of compounds potently and selectively inhibit this enzyme: nucleoside and non-nucleoside reverse transcrip-tase inhi...
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ftciteseerx:oai:CiteSeerX.psu:10.1.1.816.5630 2023-05-15T15:25:32+02:00 The Pennsylvania State University CiteSeerX Archives application/pdf http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.816.5630 http://avc.sagepub.com/content/12/1/37.full.pdf en eng http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.816.5630 http://avc.sagepub.com/content/12/1/37.full.pdf Metadata may be used without restrictions as long as the oai identifier remains attached to it. http://avc.sagepub.com/content/12/1/37.full.pdf text ftciteseerx 2022-02-27T01:25:01Z A successful strategy in the development of antiretroviral drugs has been the targetting of the virally encoded reverse transcriptase (RT) (De Clercq, 1998; Artico, 1996). Two classes of compounds potently and selectively inhibit this enzyme: nucleoside and non-nucleoside reverse transcrip-tase inhibitors (NRTIs and NNRTIs, respectively). Both play an important role in the combination therapy for HIV infection/AIDS. To date, three NNRTIs are available for clinical use: nevirapine, delavirdine and efavirenz. However, new NNRTIs that show better activity against clinically rele-vant resistant mutants are needed. Since 1992, our group has been developing dihydro-alky- Text artico Unknown |
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A successful strategy in the development of antiretroviral drugs has been the targetting of the virally encoded reverse transcriptase (RT) (De Clercq, 1998; Artico, 1996). Two classes of compounds potently and selectively inhibit this enzyme: nucleoside and non-nucleoside reverse transcrip-tase inhibitors (NRTIs and NNRTIs, respectively). Both play an important role in the combination therapy for HIV infection/AIDS. To date, three NNRTIs are available for clinical use: nevirapine, delavirdine and efavirenz. However, new NNRTIs that show better activity against clinically rele-vant resistant mutants are needed. Since 1992, our group has been developing dihydro-alky- |
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