Zobrazeno 1 - 4
of 4
pro vyhledávání: '"S. А. Lyakhov"'
Publikováno v:
Vìsnik Odesʹkogo Nacìonalʹnogo Unìversitetu: Hìmìâ, Vol 23, Iss 3(67), Pp 40-49 (2018)
DNA intercalators demonstrated a broad spectrum of terapeutic activities, such as anticancerogenic, antimicrobic and antiviral as well as ciototoxic, mutagenic and embriotoxic. One of the main marks of DNA-drug interaction is the strength of interact
Externí odkaz:
https://doaj.org/article/4df4a549699a40f3946435bff3bb2465
Autor:
K. V. Bondar, K. О. Klimenko, О. І. Alexandrova, І. А. Kravchenko, I. A. Schepetkin, S. А. Lyakhov
Publikováno v:
Vìsnik Odesʹkogo Nacìonalʹnogo Unìversitetu: Hìmìâ, Vol 21, Iss 1(57), Pp 59-71 (2016)
The purpose of this work was design planar polycyclic compounds as inhibitors of kinases, involved in the pro-inflammatory cascade. These compounds can be used as potential hits for the further anti-inflammatory drug design. Dibenzo[cd,g]indazol-6(2H
Externí odkaz:
https://doaj.org/article/bc2de6d72fce40b88695bc5bb42845a4
Publikováno v:
Vìsnik Odesʹkogo Nacìonalʹnogo Unìversitetu: Hìmìâ, Vol 23, Iss 3(67), Pp 40-49 (2018)
DNA intercalators demonstrated a broad spectrum of terapeutic activities, such as anticancerogenic, antimicrobic and antiviral as well as ciototoxic, mutagenic and embriotoxic. One of the main marks of DNA-drug interaction is the strength of interact
Autor:
S. А. Lyakhov, О. І. Alexandrova, І. А. Kravchenko, K. О. Klimenko, I. A. Schepetkin, K. V. Bondar
Publikováno v:
Vìsnik Odesʹkogo Nacìonalʹnogo Unìversitetu: Hìmìâ, Vol 21, Iss 1(57), Pp 59-71 (2016)
The purpose of this work was design planar polycyclic compounds as inhibitors of kinases, involved in the pro-inflammatory cascade. These compounds can be used as potential hits for the further anti-inflammatory drug design. Dibenzo[cd,g]indazol-6(2H