Мақаланы E-mail арқылы жіберу Synthesis of and HIV-1 Integrase Inhibition by 2-[7-(Fluorobenzyloxy)-4-Oxo-4hchromen-3-Yl]-1-Hydroxyimidazoles
- Авторлар: Nikitina P.1, Tkach I.1, Knyazhanskaya E.2, Gottikh M.2, Perevalov V.1
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Мекемелер:
- D. I. Mendeleev University of Chemical Technology of Russia
- Department of Chemistry and A. N. Belozersky Institute of Physical and Chemical Biology, Lomonosov Moscow State University
- Шығарылым: Том 50, № 8 (2016)
- Беттер: 513-518
- Бөлім: Search for New Drugs
- URL: https://journals.rcsi.science/0091-150X/article/view/244426
- DOI: https://doi.org/10.1007/s11094-016-1479-x
- ID: 244426
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Ашық рұқсат
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Аннотация
A series of six new 2-[7-(fluorobenzyloxy)-4-oxo-4H-chromen-3-yl]-1-hydroxyimidazoles were synthesized and characterized as potential HIV-1 integrase inhibitors. Prototropic tautomerism of the obtained 1-hydroxyimidazoles was discussed. Their ability to inhibit integrase catalytic activity in 3′-terminal processing and chain transfer reactions was studied. It was shown that these compounds did not exhibit noticeable inhibition.
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Авторлар туралы
P. Nikitina
D. I. Mendeleev University of Chemical Technology of Russia
Хат алмасуға жауапты Автор.
Email: polinandrevna@yandex.ru
Ресей, 9 Miusskaya Sq, Moscow, 125047
I. Tkach
D. I. Mendeleev University of Chemical Technology of Russia
Email: polinandrevna@yandex.ru
Ресей, 9 Miusskaya Sq, Moscow, 125047
E. Knyazhanskaya
Department of Chemistry and A. N. Belozersky Institute of Physical and Chemical Biology, Lomonosov Moscow State University
Email: polinandrevna@yandex.ru
Ресей, Moscow, 119991
M. Gottikh
Department of Chemistry and A. N. Belozersky Institute of Physical and Chemical Biology, Lomonosov Moscow State University
Email: polinandrevna@yandex.ru
Ресей, Moscow, 119991
V. Perevalov
D. I. Mendeleev University of Chemical Technology of Russia
Email: polinandrevna@yandex.ru
Ресей, 9 Miusskaya Sq, Moscow, 125047
