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...
Main Authors: | , , , , , , , , , , , , |
---|---|
格式: | Article |
語言: | English |
出版: |
Taylor & Francis Group
2019-01-01
|
叢編: | Journal of Enzyme Inhibition and Medicinal Chemistry |
主題: | |
在線閱讀: | http://dx.doi.org/10.1080/14756366.2018.1523901 |