FIELD: biotechnology.
SUBSTANCE: present invention relates to the field of biotechnology, in particular to a lipopeptide, aimed at inhibiting HIV, and can be used in medicine. Invention enables to obtain a polypeptide which is capable of effective inhibition of the stage of HIV penetration into a mammalian cell (human or primate), and a corresponding lipopeptide formed by conjugation of said polypeptide with a lipophilic compound, for example a fatty organic acid, or derivatives thereof. Due to its mechanism of action, the invention can be used both for therapy of HIV-infected patients, and as an agent for prevention of HIV infection.
EFFECT: in comparison with known analogues, the anti-HIV activity of the lipopeptide of the present invention is higher than the T-20 activity by several thousand times, and is also substantially higher than the activity of the known anti-HIV lipopeptides, such as C34-Chol, LP-19 or similar.
17 cl, 10 dwg, 10 ex
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Authors
Dates
2021-01-22—Published
2017-04-18—Filed