From cycloheptathiophene-3-carboxamide to oxazinone-based derivatives as allosteric HIV-1 ribonuclease H inhibitors
The paper focussed on a step-by-step structural modification of a cycloheptathiophene-3-carboxamide derivative recently identified by us as reverse transcriptase (RT)-associated ribonuclease H (RNase H) inhibitor. In particular, its conversion to a 2-aryl-cycloheptathienoozaxinone derivative and the...
Автори: | , , , , , , , , , , , , |
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Формат: | Стаття |
Мова: | English |
Опубліковано: |
Taylor & Francis Group
2019-01-01
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Серія: | Journal of Enzyme Inhibition and Medicinal Chemistry |
Предмети: | |
Онлайн доступ: | http://dx.doi.org/10.1080/14756366.2018.1523901 |