Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nathaly Shvets"'
Autor:
Bedia, Koçyiğit-Kaymakçıoğlu, Elçin, Oruç, Seda, Unsalan, Fatma, Kandemirli, Nathaly, Shvets, Sevim, Rollas, Dimoglo, Anatholy
Publikováno v:
In European Journal of Medicinal Chemistry 2006 41(11):1253-1261
Autor:
Hakan Sezgin Sayiner, Nathaly Shvets, Turgay Polat, Anatholy Dimoglo, Murat Basaran, Can Dogan Vurdu, Vasyl Kovalish, Fatma Kandemirli
Publikováno v:
Medicinal Chemistry. 11:77-85
That the implementation of Electronic-Topological Method and a variant of Feed Forward Neural Network (FFNN) called as the Associative Neural Network are applied to the compounds of Hydrazones derivatives have been employed in order to construct mode
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a788571976f614282f67cba46188f745
https://doi.org/10.2174/1573406410666140428144334
https://doi.org/10.2174/1573406410666140428144334
Autor:
Nathaly Shvets, Athina Geronikaki, Anatholy Dimoglo, Robert C. Reynolds, Serghei Pogrebnoi, Fliur Macaev, Veaceslav Boldescu, Zinaida Ribkovskaia, Ghenadie Rusu
Publikováno v:
Bioorganic & Medicinal Chemistry. 19:6792-6807
A series of 82 5-aryl-2-thio-1,3,4-oxadiazole derivatives were screened for their anti-mycobacterial activities against Mycobacterium tuberculosis H37Rv. The synthesized compounds 30–37 appeared to be the most active derivatives exhibiting more tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a9316137e2faf1bb013e32d07768bae
https://doi.org/10.1016/j.bmc.2011.09.038
https://doi.org/10.1016/j.bmc.2011.09.038
Autor:
Nathaly Shvets, Anatholy Dimoglo, Fatma Kandemirli, Aysel Gürsoy, Süheyla Özbey, Nilgün Karalı, F. Betül Kaynak, Vasyl Kovalishyn
Publikováno v:
Bioorganic & Medicinal Chemistry. 15:5888-5904
New series of 5-fluoro-1H-indole-2,3-dione-3-thiosemicarbazones 2a-k and 5-fluoro-1-morpholino/piperidinomethyl-1H-indole-2,3-dione-3-thiosemicarbazones 3a-r were synthesized. The structures of the synthesized compounds were confirmed by spectral dat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bfcfc803cc5f83054f5ad59740e4fba
https://doi.org/10.1016/j.bmc.2007.05.063
https://doi.org/10.1016/j.bmc.2007.05.063
Autor:
Eugenia Stingaci, Serghei Pogrebnoi, Nathaly Shvets, Anatholy Dimoglo, Ghenadie Rusu, Robert C. Reynolds, Ludmila Vlad, Fatma Kandemirli, Alexandru Gudima, Fliur Macaev
Publikováno v:
Bioorganic & Medicinal Chemistry. 13:4842-4850
The preparation of novel 5-aryl-2-thio-1,3,4-oxadiazoles 4a-41 and the computer-aided study of their in vitro anti-tubercular activity against Mycobacterium tuberculosis H37Rv (ATCC 27294) are reported. The average accuracy of the electronic-topologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67122df3d262f87b8c594bdc84cfea1b
https://doi.org/10.1016/j.bmc.2005.05.011
https://doi.org/10.1016/j.bmc.2005.05.011
Publikováno v:
Journal of Medicinal Chemistry. 47:6760-6767
A series of 2,5-disubstituted-1,3,4-thiadiazoles were synthesized, the compounds structures were elucidated and screened for the antituberculosis activity against Mycobacterium tuberculosis H37Rv using the BACTEC 460 radiometric system. Among the tes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e268b7ad1a11119b91cd9eb7a33078ae
https://doi.org/10.1021/jm0495632
https://doi.org/10.1021/jm0495632
Autor:
Anatholy Dimoglo, Nathaly Shvets, Fatma Budak, Fatma Kandemirli, Hikmet Agirbas, Vasyl Kovalishyn, Sema Aşkın Keçeli, Selahaddin Guner
Publikováno v:
Bioorganicmedicinal chemistry. 15(6)
The synthesis of 2,3,5-substituted perhydropyrrolo[3,4-d]isoxazole-4,6-diones (44 compounds) has been accomplished by the cycloaddition reaction of N-methyl-C-arylnitrones with N-substituted maleimides. The compounds were screened for their antibacte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca4e608261a91db1f93a49821237d15c
https://pubmed.ncbi.nlm.nih.gov/17276071
https://pubmed.ncbi.nlm.nih.gov/17276071
Publikováno v:
Journal of molecular graphicsmodelling. 25(1)
Structure-activity relationships study was performed for a series of Schiff bases hydroxysemicarbazide as potential antitumor agents by using the electronic-topological method combined with neural networks (ETM-NN). Data for the approach were obtaine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03142f9893ca3b8f7e65de3d96736dff
https://pubmed.ncbi.nlm.nih.gov/16310387
https://pubmed.ncbi.nlm.nih.gov/16310387