Zobrazeno 1 - 10
of 25
pro vyhledávání: '"N K, Vlasenkova"'
Autor:
O. V. Goryunova, G. N. Apryshko, L. V. Fetisova, R. B. Pugacheva, O. S. Zhukova, N. K. Vlasenkova
Publikováno v:
Russian Journal of Biotherapy. 16:46-54
Objective: to evaluate the prospects of the glycosides of indolocarbazole containing amino acid residues as potential antitumor compounds. Materials and methods. For 32 compounds by structural formulas using the methods of chemoinformatics, a number
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d41e8dafd904ef0b010363c7e2b90cf9
https://doi.org/10.17650/1726-9784-2017-16-4-46-54
https://doi.org/10.17650/1726-9784-2017-16-4-46-54
Publikováno v:
Russian Journal of Biotherapy. 15:70-78
Background. Concentration of a prostate specific antigen (PSA) in blood serum considerably increases in case of development of a prostate adenocarcinoma, in tens and hundreds times exceeding extreme values of the range of the determined concentration
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88f62a3fef8b0509202420f6aa8e12e2
https://doi.org/10.17650/1726-9784-2016-15-3-70-78
https://doi.org/10.17650/1726-9784-2016-15-3-70-78
Autor:
G. K. Gerasimova, Sergey G. Klochkov, S. V. Afanas’eva, Yu. N. Bulychev, A. N. Pushin, N. K. Vlasenkova
Publikováno v:
Chemistry of Natural Compounds. 45:817-823
Previously unknown amino-derivatives of the natural sesquiterpene lactone α-santonin were synthesized. The activity of the products against several human tumor-cell lines was studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e90a4b851031a6bc81ecfd108a0d1393
https://doi.org/10.1007/s10600-010-9499-3
https://doi.org/10.1007/s10600-010-9499-3
Autor:
A.P. Kaplun, V. I. Shvets, E L Surkova, A. V. Symon, N. K. Vlasenkova, G. K. Gerasimova, E F Litvin, L M Kozlova, Le Bang Shon
Publikováno v:
Russian Journal of Bioorganic Chemistry. 29:185-189
Two methods of obtaining of 3 alpha-betulinic acid and related compounds from their 3 beta-epimers were studied: the reaction of bimolecular substitution and the stereoselective reduction of 3-ketoderivatives. The substitution of acyloxy by formyloxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e91e1eea81b3cfb5bd024c8aa1311865
https://doi.org/10.1023/a:1023220701797
https://doi.org/10.1023/a:1023220701797
Publikováno v:
Pharmaceutical Chemistry Journal. 30:213-216
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b10f9330cd0dc01175cbdb5db3861ab1
https://doi.org/10.1007/bf02218763
https://doi.org/10.1007/bf02218763
Publikováno v:
Vestnik Rossiiskoi akademii meditsinskikh nauk. (10)
A4 clone cells, received by CD95-mediated selection from the parental line of Jurkat T-lymphoblast human leukosis, lost their ability of apoptosis as a result of programmed cell death mechanism breakdown. The complex of their acquired phenotypic prop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::82d5a32e863a60a87c0a46c0227b20c0
https://pubmed.ncbi.nlm.nih.gov/18050680
https://pubmed.ncbi.nlm.nih.gov/18050680
Autor:
A.P. Kaplun, G. K. Gerasimova, V. I. Shvets, N. N. Veselova, A. V. Symon, A. I. Lyutik, G. A. Fedorova, N. K. Vlasenkova
Publikováno v:
Bioorganicheskaia khimiia. 31(3)
New cyclopropane derivatives of betulin were synthesized by attachment of dichlorocarbenes or dibromocarbenes to the double bond of betulin diacetate, followed by the deprotection of hydroxyl groups. The betulin cyclopropane derivative was obtained f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06a46a5b5eb9a8d441ccfb99e7006d22
https://pubmed.ncbi.nlm.nih.gov/16004391
https://pubmed.ncbi.nlm.nih.gov/16004391
Autor:
A V, Symon, A P, Kaplun, N K, Vlasenkova, G K, Gerasimova, Le Bang, Shon, E F, Litvin, L M, Kozlova, E L, Surkova, V I, Shvets
Publikováno v:
Bioorganicheskaia khimiia. 29(2)
Two methods of obtaining of 3 alpha-betulinic acid and related compounds from their 3 beta-epimers were studied: the reaction of bimolecular substitution and the stereoselective reduction of 3-ketoderivatives. The substitution of acyloxy by formyloxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f5a796e82b1a413c8fa7d8a85185b86
https://pubmed.ncbi.nlm.nih.gov/12708322
https://pubmed.ncbi.nlm.nih.gov/12708322
Autor:
A. V. Symon, N. N. Veselova, A.P. Kaplun, N. K. Vlasenkova, G. A. Fedorova, A. I. Lyutik, G. K. Gerasimova, V. I. Shvets
Publikováno v:
Russian Journal of Bioorganic Chemistry; May2005, Vol. 31 Issue 3, p286-291, 6p
Publikováno v:
European Journal of Cancer Supplements. 1:S294-S295
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd4cee42d4c2135458d9ed08101a831b
https://doi.org/10.1016/s1359-6349(03)91009-3
https://doi.org/10.1016/s1359-6349(03)91009-3