Zobrazeno 1 - 10
of 34
pro vyhledávání: '"L M Korkodinova"'
Publikováno v:
RUDN Journal of Medicine, Vol 0, Iss 3, Pp 197-200 (2010)
There was investigated the possibility of using the service Web 2.0 while carrying out a distance course on pharmaceutical chemistry. The methodology of holding Internet seminar was described, the results were analysed.
Externí odkaz:
https://doaj.org/article/e2cf1ca8db89445db1db72438dab0fb5
Publikováno v:
RUDN Journal of Medicine, Vol 0, Iss 4, Pp 165-167 (2010)
The physical and chemical properties were studied; the metodics of proof the identity, good quality and quantitative analysis of substance of amide N-allylanthranylic acid are developed. This substance was recommended for predclinical investigation a
Externí odkaz:
https://doaj.org/article/c9e9a5dafa714aac8e9bfc00cda5d3a2
Publikováno v:
RUDN Journal of Medicine, Vol 0, Iss 4, Pp 295-297 (2010)
The amide of N-allylanthranylic acid was synthesized; the structure was confirmed by IR-, IMR- and chromate-mass spectra, the anti-inflammatory, analgesic, antipyretic, ulcer, antihypoxic activities and acute toxicity were studied.
Externí odkaz:
https://doaj.org/article/c7fe80e920ec4e91a58a6d0dc2a37e5a
Publikováno v:
Pharmaceutical Chemistry Journal. 56:1060-1063
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bd701af27a285922f45d152721f1ff8
https://doi.org/10.1007/s11094-022-02753-5
https://doi.org/10.1007/s11094-022-02753-5
Autor:
K. V. Andryukov, L. M. Korkodinova
Publikováno v:
Pharmaceutical Chemistry Journal. 56:889-893
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56d84914ebbf3d56aba9ccf5e72f172e
https://doi.org/10.1007/s11094-022-02723-x
https://doi.org/10.1007/s11094-022-02723-x
Autor:
A. A. Kurbatova, R. R. Makhmudov, L. M. Korkodinova, A. F. Gazizova, E. R. Kurbatov, A. A. Bobyleva
Publikováno v:
Pharmaceutical Chemistry Journal. 52:965-968
A series of R-benzylidenehydrazides of NH-furoyl-5-iodoanthranilic acid were synthesized by condensing NH-furoyl-5-iodoanthranilic acid hydrazide with aromatic aldehydes. Their structures were confirmed using IR and PMR spectroscopy. Their analgesic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f9ca06db1fe872b80259b9e1b6eabae
https://doi.org/10.1007/s11094-019-01934-z
https://doi.org/10.1007/s11094-019-01934-z
Autor:
L. M. Korkodinova, K. V. Andryukov
Publikováno v:
Medicina. 7:94-109
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0eeb3dcaab86d54f89951616e1362864
https://doi.org/10.29234/2308-9113-2019-7-4-94-109
https://doi.org/10.29234/2308-9113-2019-7-4-94-109
Autor:
K. V. Andryukov, L. M. Korkodinova
Publikováno v:
Pharmaceutical Chemistry Journal. 52:411-414
Molecular docking of 22 N-aroyl-substituted halo(H)anthranilic acid amides and hydrazides with cyclooxygenase 1 (COX1) is described. The dependence of anti-inflammatory activity (AIA) on scoring functions (BeCOX1, ImeCOX1, KiCOX1) and lipophilicity c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::620debe2927c56f3b41d08a67ba13370
https://doi.org/10.1007/s11094-018-1832-3
https://doi.org/10.1007/s11094-018-1832-3
Autor:
L. M. Korkodinova, K. V. Andryukov
Publikováno v:
Pharmaceutical Chemistry Journal. 50:159-164
Ionization constants (pKa and pKb) of N-substituted mono(di)halo(H)anthranilic acids and their amides and hydrazides were studied as functions of their quantum-chemical parameters. The predicted pKa and pKb values calculated for 10 new compounds of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68262a3c1be3dcdc6adad7ce8d4800f9
https://doi.org/10.1007/s11094-016-1415-0
https://doi.org/10.1007/s11094-016-1415-0
Autor:
L. G. Mardanova, E. R. Kurbatov, A. G. Gol’dshtein, L. M. Korkodinova, T. I. Yarygina, A. S. Botalova
Publikováno v:
Pharmaceutical Chemistry Journal. 48:791-794
N-Substituted 5-iodo(H)anthranilic acid amides were synthesized by acylation of 5-iodoanthranilic acid amide in benzene with heating and by alkylation of anthranilic acid amide at room temperature. The synthesized compounds were studied for analgesic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26cc632d347c651ee4a0c49951b9d03f
https://doi.org/10.1007/s11094-015-1197-9
https://doi.org/10.1007/s11094-015-1197-9