FIELD: medicine, pharmacology.
SUBSTANCE: compound formula I is described, including the pharmaceutically acceptable salts, , where: Z presents ; Q is taken from the group that consists of: -W - presents , and the pharmaceutical composition, application of compound formula (I) for preparation of antiviral medicine.
EFFECT: proposed compounds can be helpful in treatment of HIV and AIDS.
70 cl, 2 tbl, 129 ex
Title | Year | Author | Number |
---|---|---|---|
NOVEL COMPOUNDS THAT ARE ERK INHIBITORS | 2013 |
|
RU2660429C2 |
MONOMER DERIVATIVES OF GLYCOPEPTIDE ANTIBIOTIC | 2005 |
|
RU2424248C2 |
AZAINDOLEOXOACETIC DERIVATIVES OF PIPERAZINE AND PHARMACEUTICAL COMPOSITION BASED ON THEREOF | 2002 |
|
RU2303038C2 |
NEMATOCIDAL SULPHONAMIDES | 2010 |
|
RU2531317C2 |
DERIVATIVES OF PYRAZIOLE WITH CONDENSED CYCLE | 2002 |
|
RU2318822C2 |
BRIDGED N-CYCLYC SULPHONAMIDO-INHIBITORS OF GAMMA-SECRETASE | 2006 |
|
RU2422443C2 |
COMPOUNDS AND COMPOSITIONS FOR THE TREATMENT OF CONDITIONS ASSOCIATED WITH NLRP ACTIVITY | 2019 |
|
RU2795108C2 |
ARYL, HETEROARYL AND HETEROCYCLIC COMPOUNDS FOR TREATMENT OF COMPLEMENT-MEDIATED DISORDERS | 2015 |
|
RU2707749C2 |
HETEROCYCLIC COMPOUNDS, EFFECTIVE FOR KINASE INHIBITION | 2011 |
|
RU2640862C2 |
INHIBITION OF CREB-BINDING PROTEIN (CBP) | 2019 |
|
RU2803290C2 |
Authors
Dates
2008-05-10—Published
2003-04-30—Filed