Zobrazeno 1 - 10
of 16
pro vyhledávání: '"M. V. Jasko"'
Publikováno v:
Molecular Biology. 55:624-636
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01aa847a2dac14fcbe469c0ad49e9696
https://doi.org/10.1134/s0026893321030146
https://doi.org/10.1134/s0026893321030146
Autor:
S. D. Negrya, M. V. Jasko, D. A. Makarov, P. N. Solyev, I. L. Karpenko, O. V. Shevchenko, O. V. Chekhov, A. A. Glukhova, B. F. Vasilyeva, T. A. Efimenko, I. G. Sumarukova, O. V. Efremenkova, S. N. Kochetkov, L. A. Alexandrova
Publikováno v:
Molecular Biology. 55:143-153
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6076586e53eda844ed7b86a1bcb25fd9
https://doi.org/10.1134/s002689332101012x
https://doi.org/10.1134/s002689332101012x
Publikováno v:
Molekuliarnaia biologiia. 55(4)
Hydrophobic molecules may be toxic when present in excess. When dissolved in membranes, hydrophobic molecules disrupt membrane function. Studies on the effects of free fatty acids (FFA) on cultured cells contradict each other. Here we describe the ef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::936c6c4da4924d22f5dea6f4da2b44fc
https://pubmed.ncbi.nlm.nih.gov/34432786
https://pubmed.ncbi.nlm.nih.gov/34432786
Autor:
S D, Negrya, M V, Jasko, D A, Makarov, P N, Solyev, I L, Karpenko, O V, Shevchenko, O V, Chekhov, A A, Glukhova, B F, Vasilyeva, T A, Efimenko, I G, Sumarukova, O V, Efremenkova, S N, Kochetkov, L A, Alexandrova
Publikováno v:
Molekuliarnaia biologiia. 55(1)
Resistance developed to the majority of drugs used to treat infectious diseases warrants the design of new compounds effective against drug-resistant strains of pathogens. Recently, several groups of modified nucleosides have been synthesized and sho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::463180e993b340c1ee950b3c598a50a0
https://pubmed.ncbi.nlm.nih.gov/33566035
https://pubmed.ncbi.nlm.nih.gov/33566035
Publikováno v:
Acta Naturae
As has been shown previously, phosphite of acycloguanosine (Hp-ACG) exhibits equal efficacy against ACV-sensitive and ACV-resistant HSV-1 strains in cell culture. Intraperitoneal administration of Hp-ACG to model mice with herpetic encephalitis cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3edd4af229c90794a1d931d6c571eb08
https://pubmed.ncbi.nlm.nih.gov/27099786
https://pubmed.ncbi.nlm.nih.gov/27099786
Publikováno v:
Russian Journal of Bioorganic Chemistry. 37:578-585
A series of new acyclovir phosphoramidates—potential antiviral agents against resistant strains of herpes virus—was synthesized. Of several approaches used for their synthesis, the treatment of the intermediate phosphorochloridate with various am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92cafa7e4690931fd6da09ee42cb3675
https://doi.org/10.1134/s1068162011050190
https://doi.org/10.1134/s1068162011050190
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 46:669-676
New approaches to the synthesis of 3′-azido-3′-deoxythymidine labelled with tritium in the heterocyclic base have been developed. With this aim, enzymatic transribosylation with [3H]thymine using the enzyme preparation from rat liver and a three-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efd7bf6f078ee817c78c4d8ba3a50143
https://doi.org/10.1002/jlcr.707
https://doi.org/10.1002/jlcr.707
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 50:585-587
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c38e13039eddaf95f428501160c55db4
https://doi.org/10.1002/jlcr.1287
https://doi.org/10.1002/jlcr.1287
Publikováno v:
ChemInform. 35
A new synthesis of chiral acyclic nucleoside and nucleotide analogues starting from d (−)- or l (+)-riboses was proposed. Antiviral properties of the synthesized compounds towards the pox virus family were evaluated.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f93ce78635e80a8b35c34616e243141
https://doi.org/10.1002/chin.200441199
https://doi.org/10.1002/chin.200441199
Autor:
E. De Clercq, J.-L. Imbach, G. V. Gurskaya, J. Balzarini, M. V. Jasko, E. M. Kazmina, J.-P. Sommadossi, Abdesslem Faraj, I. Fedorov, V. E. Zavodnic, G. Gosselin
Publikováno v:
Journal of medicinal chemistry. 40(4)
A synthetic scheme for the 3'-oxime derivatives 3E, 5E, 5Z, 7E and 7Z of 1-(2,3-dideoxy-beta-D-glycero-pentofuranosyl)thymine and for 1-(2,3-dideoxy-3-nitro-beta-D-erythro-pentofuranosyl)-thymine (10) has been developed starting from appropriately 5'
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9668899ba2eac49d89a0a69ffe0286b9
https://pubmed.ncbi.nlm.nih.gov/9046339
https://pubmed.ncbi.nlm.nih.gov/9046339