Zobrazeno 1 - 10
of 106
pro vyhledávání: '"F. S. Zarudii"'
Autor:
T. A. Sapozhnikova, A. V. Koval’skaya, Inna P. Tsypysheva, P. R. Petrova, Alexander N. Lobov, N. S. Makara, F. S. Zarudii, S. F. Gabdrakhmanova
Publikováno v:
Natural Product Research. 35:207-215
Novel derivatives of 4-oxo-3-methylcytisine with phenyl moiety bonded to starting molecule through various spacers were obtained from the 9-amino, -halo, -formyl and 11-halo precursors by reductive alkylation of amines, generation of amide, as well a
Autor:
P. R. Petrova, N. S. Makara, F. S. Zarudii, Sophia S. Borisevich, C L. Khursan, R. Yu. Khisamutdinova, T. A. Sapozhnikova, Inna P. Tsypysheva, A. V. Koval’skaya
Publikováno v:
Bulletin of Experimental Biology and Medicine. 164:434-438
We performed screening of nootropic properties of 10 new derivatives of quinolizidine alkaloid (-)-cytisine. Compounds with β-endo stereochemistry were more active than α-endo-isomers. Under stress conditions (3aR,4S,8S,12R,12aS,12bR)-10-methyl-2-p
Publikováno v:
Pharmaceutical Chemistry Journal. 51:884-888
Thymidylate synthase (ThS) is a target for antimetabolite antitumor drugs. Such drugs have been used in the clinic although they cause several severe side effects and accumulate in tissues. Therefore, new less toxic ThS inhibitors must be sought and
Autor:
N.N. Gibadullina, Sergey L. Khursan, T. A. Sapozhnikova, R. Yu. Khisamutdinova, D.R. Kireeva, S. F. Gabdrakhmanova, N. S. Makara, F. S. Zarudii, Sophia S. Borisevich
Publikováno v:
Behavioural brain research. 373
The neurodegenerative diseases have a complex pathogenetic mechanism comprising oxidative stress and receptor system dysfunction caused by various damaging factors such as, for example, brain hypoxia. The purpose of this study was to elucidate the in
Autor:
N. S. Makara, F. S. Zarudii, S. S. Lyashenko, R. Yu. Khisamutdinova, T. A. Sapozhnikova, S. G. Yunusova, M. S. Yunusov, S. F. Gabdrakhmanova, O. N. Denisenko, Z. V. Ishchenko
Publikováno v:
Chemistry of Natural Compounds. 52:973-978
The compositions of neutral lipids (NL) and fatty acids (FA) from subterranean parts of the introduced plants Helleborus abchasicus and H. caucasicus (Ranunculaceae) were established and compared with those of the wild species. The FA from diacyl- an
Autor:
A. S. Budaev, N. S. Makara, Leonid V. Spirikhin, F. S. Zarudii, Baltina Lidiya A, L. R. Mikhailova
Publikováno v:
Chemistry of Natural Compounds. 52:441-444
New 2-hydroxy-1-en-3-ones were prepared by oxidation of 11-deoxoglycyrrhetic acid 3-oxo-derivatives and its 30-methyl ester by atmospheric oxygen in the presence of t-BuOK. 2-Hydroxy-3-oxo-18βH-olean-1,12-dien-30-oic acid at a dose of 50 mg/kg reduc
Publikováno v:
Chemistry of Natural Compounds. 52:82-85
The antihypoxic activity of a series of quinopimaric acid scaffold derivatives was studied. It was shown that compounds 3, 5, and 8 increased the lifespan of mice in various hypoxia models.
Publikováno v:
Pharmaceutical Chemistry Journal. 49:582-586
Docking of a series of methanepyrido[1,2-a][1,5]diazocin[(-)-cytisine derivatives to the active center of the nicotinic acetylcholine receptor was used to generate a set of potential substances for the treatment of cognitive dysfunction. The results
Autor:
N. S. Makara, S. F. Gabdrakhmanova, T. A. Sapozhnikova, R. Yu. Khisamutdinova, A. R. Uzbekov, F. S. Zarudii, G. F. Vafina
Publikováno v:
Pharmaceutical Chemistry Journal. 51:348-350
The hepatoprotective and choleretic activities of three levopimaric acid derivatives were studied experimentally using a CCl4-induced acute hepatitis model in rats. It was established that all investigated levopimaric acid derivatives tended to incre
Autor:
Sergey L. Khursan, P. R. Petrova, F. S. Zarudii, Yulia V. Vakhitova, Nina S Makara, L. F. Zainullina, Sophia S. Borisevich, A. V. Koval’skaya, Inna P. Tsypysheva
Publikováno v:
Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry. 16
Background and objectives Neurodegenerative diseases and inflammation are always linked to each other; therefore the elaboration of new chemical compounds, which interact with pharmacological targets involved into these two processes, can become one