Zobrazeno 1 - 10
of 17
pro vyhledávání: '"V V, Bychko"'
Autor:
A. V. Kravchenko, E. A. Orlova-Morozova, T. E. Shimonova, O. A. Kozyrev, F. I. Nagimova, N. G. Zaharova, E. S. Ivanova, U. A. Kuimova, A. A. Popova, O. E. Chernova, O. S. Tonkih, D. A. Gusev, A. A. Yakovlev, V. V. Pokrovsky, V. V. Bychko, N. V. Vostokova
Publikováno v:
Журнал инфектологии, Vol 10, Iss 2, Pp 76-82 (2018)
A randomized multicenter 96-week study of an elsulfavirine (ESV), non-nucleoside reverse transcriptase inhibitor (NNRTI) of novel generation, in combination with 2 nucleoside/ nucleotide reverse transcriptase inhibitors (NRTIs) was conducted in naive
Externí odkaz:
https://doaj.org/article/ccd16d06c41c4c1cac7a9639593806e6
Autor:
Ya. A. Ivanenkov, Pavel M. Yamanushkin, V. M. Kisil, A. V. Ivashchenko, Ilya Okun, Andrey Alexandrovich Ivashchenko, Oleg D. Mitkin, O. M. Korzinov, V. Yu. Vedenskii, Elena A. Bulanova, I. A. Leneva, V. V. Bychko
Publikováno v:
Pharmaceutical Chemistry Journal. 48:569-581
New substituted ethyl esters of 2,4-bis-aminomethyl-5-hydroxy-1H-indole-3-carboxylic acids, 8-aminomethyl-2-methyl-2,3-dihydro-1H,7H-[1,3]-oxazino-[5,6-e]indole-9-carboxylic acids, and members of the previously unknown 4,5-dihydro-1H-pyrrolo[4,3,2-de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab6ba4b403608202e67e772c93b5a88a
https://doi.org/10.1007/s11094-014-1153-0
https://doi.org/10.1007/s11094-014-1153-0
Autor:
V. V. Bychko, O. M. Korzinov, Oleg D. Mitkin, V. Yu. Vedenskii, Elena A. Bulanova, Ilya Okun, I. A. Leneva, V. M. Kisil, Pavel M. Yamanushkin, A. V. Ivashchenko
Publikováno v:
Pharmaceutical Chemistry Journal. 47:636-650
New substituted ethyl 5-hydroxy-1,2-dimethyl-1H-indole-3-carboxylates and 7,8-dimethyl-1,2,3,7-tetrahydro[1,3]oxazino[5,6-e]indole-9-carboxylates including arbidol analogs in addition to 6-hydroxy-1-methyl-7-pyridin-3-yl-4,5-dihydropyrrolo[4,3,2-de]i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e23f0986ebe8fd93a1ef424e142f867
https://doi.org/10.1007/s11094-014-1024-8
https://doi.org/10.1007/s11094-014-1024-8
Autor:
A V, Ivashchenko, P M, Iamanushkin, O D, Mit'kin, E V, Ezhova, O M, Korzinov, N A, Shevkun, R N, Karapetian, V V, Bychko, A A, Ivashchenko, V Z, Agrba, B A, Lapin, S V, Orlov, I É, Kuznetsov
Publikováno v:
Eksperimental'naia i klinicheskaia farmakologiia. 77(12)
Pharmacological safety of a new type of HCV inhibitor, AV0012, was studied including acute, subchronic and chronic toxicity in mice, rats and monkeys. Genotoxicity was assessed using the Ames test and the chromosomal aberrations assay in the bone mar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::88c7b5d647832b8fd86d6c612609638c
https://pubmed.ncbi.nlm.nih.gov/25739191
https://pubmed.ncbi.nlm.nih.gov/25739191
Autor:
A V, Ivashchenko, P M, Iamanushkin, O D, Mit'kin, E V, Ezhova, O M, Korzinov, E A, Bulanova, A G, Koriakova, P V, Vyshemirskaia, V V, Bychko, A A, Ivashchenko
Publikováno v:
Eksperimental'naia i klinicheskaia farmakologiia. 77(10)
Several novel compounds were found to be potent inhibitors of the HCV (JFH-1 isolate) infection in vitro. Human serum did not significantly reduce antiviral activity of the lead compound, AVR560 (4-fold). The immunohistochemistry studies with the Huh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c40297c81961976f6e1c9cc1bc0a8e21
https://pubmed.ncbi.nlm.nih.gov/25518527
https://pubmed.ncbi.nlm.nih.gov/25518527
Autor:
A V, Ivashchenko, P M, Iamanushkin, O D, Mit'kin, E V, Ezhova, O M, Korzinov, N A, Shevkun, A G, Koriakova, R N, Karapetian, V V, Bychko, A A, Ivashchenko, V Z, Agrba, B A, Lapin, S V, Orlov
Publikováno v:
Eksperimental'naia i klinicheskaia farmakologiia. 77(4)
In vitro immunohistochemical investigations on the human hepatoma cell line (Huh7) infected with hepatitis C virus (HCV) strain JFH-1 showed that AV0012 compound blocks the early stages of viral infection. AV0012 also blocked viral infection spread i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f29b1a9a6f0951f98c0ee0a50cf7892b
https://pubmed.ncbi.nlm.nih.gov/25076758
https://pubmed.ncbi.nlm.nih.gov/25076758
Autor:
M A, Bundule, V V, Bychko, Iu B, Saulitis, E E, Liepin'sh, G P, Borisova, I A, Petrovskiĭ, V V, Tsibinogin, P P, Pumpen, E Ia, Gren
Publikováno v:
Doklady Akademii nauk SSSR. 312(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d0c2bf94c89e3148f89971fd895fa678
https://pubmed.ncbi.nlm.nih.gov/2226141
https://pubmed.ncbi.nlm.nih.gov/2226141
Publikováno v:
Doklady Akademii nauk SSSR. 274(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c9a3294a4731ff0214f025bf63153aa5
https://pubmed.ncbi.nlm.nih.gov/6373205
https://pubmed.ncbi.nlm.nih.gov/6373205
Publikováno v:
Bioorganicheskaia khimiia. 12(3)
The nucleotide sequence of the 3'-terminal region of the cloned bovine leukaemia virus cDNA (1474 bp) was elucidated using both Sanger and Maxam-Gilbert techniques. This DNA region contains U3 and R parts of the BLV LTR and an upstream sequence with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::89c9cb1c4e39067f9baacee047107c82
https://pubmed.ncbi.nlm.nih.gov/3008763
https://pubmed.ncbi.nlm.nih.gov/3008763
Publikováno v:
Molekuliarnaia biologiia. 15(5)
A series of plasmids with tetracycline resistance genes (Tcr-operon) subjected to transcription from chloramphenicol acetyl transferase promoter (Cmr-promoter) have been constructed on the basis of plasmid pBR325, AprCmrTcr. For this purpose, a 0.8 M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::72c60e1f805daeeaa2040f7b0abeffb0
https://pubmed.ncbi.nlm.nih.gov/7029244
https://pubmed.ncbi.nlm.nih.gov/7029244