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Ruthenium arene complexes as HIV-1 integrase strand transfer inhibitors
The quinolone HL1 and the hydroxypyrimidine-carboxamide HL2 were designed and synthesized as models of the HIV integrase strand transfer inhibitors Elvitegravir and Raltegravir (brand name Isentress), with the aim to study their complexing behavior and ...
Alessia Bacchi +2 more
exaly +2 more sources
The life cycle of HIV-1 requires extensive assistance from the integrase (IN) enzyme which therefore constitutes an attractive therapeutic target for the development of anti-AIDS agents. We herein report the synthesis and biological evaluation of new HIV
Frauke Christ +2 more
exaly +3 more sources
A novel HIV-1 integrase mutation pattern, L74F V75I, which conferred resistance to first-generation integrase strand transfer inhibitors (INSTIs), was identified in a clinical case with virological failure under a raltegravir-based regimen.
Yasumasa Iwatani +2 more
exaly +2 more sources
<p>The development of resistance to human immunodeficiency virus 1 (HIV-1) integrase strand-transfer inhibitors (INSTI) has been documented; however, knowledge of the impact of pre-existing integrase (IN) mutations on INSTI resistance (INSTI-R) is
Nicolas A Margot +2 more
exaly +2 more sources
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Advances in the development of HIV integrase strand transfer inhibitors
European Journal of Medicinal Chemistry, 2021Renhua Fan, Shuang-Xi Gu, Qiuqin He
exaly
Integrase strand transfer inhibitors in the management of HIV-positive individuals
Annals of Medicine, 2014Veronica Zanichelli +2 more
exaly

