Zobrazeno 1 - 10
of 14
pro vyhledávání: '"I G, Tsygankova"'
Autor:
I. G. Tsygankova, S. M. Zhenodarova
Publikováno v:
Russian Journal of General Chemistry. 81:2320-2327
The structure-property correlation relation based on the fragment descriptors of molecular structure was used for the calculation of the apoptosis-inducing activity of 3,5-diaryl-1,2,4-oxadiazoles. A set of the correlation models of similar accuracy,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a30a12423d3f8e4a5fd182f6c603d1b
https://doi.org/10.1134/s107036321111017x
https://doi.org/10.1134/s107036321111017x
Autor:
I. G. Tsygankova, S. M. Zhenodarova
Publikováno v:
Russian Journal of General Chemistry. 81:913-919
The structure-property correlation based on the fragment description of the molecular structure is used for the calculation of the antiproliferative and apoptosis-inducing activity of a series of the trans- and cis-stilbene derivatives and related co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0a49b8d766a5d6604a38a9289a1d8c0
https://doi.org/10.1134/s1070363211050124
https://doi.org/10.1134/s1070363211050124
Autor:
S. M. Zhenodarova, I. G. Tsygankova
Publikováno v:
Russian Journal of General Chemistry. 79:488-495
The correlation structure- property was used for the calculation of inhibitor activity of a series of isatin derivatives, inhibitors of caspase 3, based on a fragment description of the molecular structure. A large number of simple models of the simi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7cdf05be0f6a1462234c1a5386837bc
https://doi.org/10.1134/s1070363209030244
https://doi.org/10.1134/s1070363209030244
Autor:
S. M. Zhenodarova, I. G. Tsygankova
Publikováno v:
Russian Journal of General Chemistry. 78:1760-1766
Structure-property relationship based on fragment descriptors of molecular structure was used to assess the ability of phenol derivatives to induce apoptosis in L1210 leukemia cells in mice. Simple models that provide quite accurate estimates for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4829e90761b8c5fc933a2f9fba55336
https://doi.org/10.1134/s1070363208090181
https://doi.org/10.1134/s1070363208090181
Autor:
S. M. Zhenodarova, I. G. Tsygankova
Publikováno v:
Russian Journal of General Chemistry. 77:940-948
A previously suggested quantitative structure-property relationship was applied to estimation of the depressant action time of barbituric acid derivatives, using a set of 107 compounds as example. To choose molecular descriptors and decrease the numb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d30cdaa6e3456c43737df0d099bebfc4
https://doi.org/10.1134/s1070363207050222
https://doi.org/10.1134/s1070363207050222
Autor:
S. M. Zhenodarova, I. G. Tsygankova
Publikováno v:
Russian Journal of General Chemistry. 76:1618-1624
The quantitative structure-property relationship was used for estimating the activity of influenza virus neuraminidase inhibitors, cyclohexene and cyclopentane derivatives. Application of two models, topological and geometric, showed that in both cas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cef40495c288e9105f5b57eec573d417
https://doi.org/10.1134/s1070363206100203
https://doi.org/10.1134/s1070363206100203
Publikováno v:
Russian Journal of General Chemistry. 76:267-271
A structure-property relationship was used to estimate the free energy of formation of host-guest complexes of α-cyclodextrin with monosubstituted benzene and phenol derivatives and with symmetrical 1,4-disubstituted benzene derivatives, in which va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b9b316bff0d1a42b6258db35d0f47d0
https://doi.org/10.1134/s1070363206020186
https://doi.org/10.1134/s1070363206020186
Autor:
I. B. Golovanov, I. G. Tsygankova
Publikováno v:
Russian Journal of General Chemistry. 71:1584-1588
A structure-property relationship is proposed, that allows a fairly accurate estimation of log P for amides of carboxylic acids and their N-acetyl derivatives.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08c81fd5c95a272afab460dcfc8e3c90
https://doi.org/10.1023/a:1013907221271
https://doi.org/10.1023/a:1013907221271
Autor:
I. B. Golovanov, I. G. Tsygankova
Publikováno v:
Russian Journal of General Chemistry. 71:833-838
The molecule surface area accessible for a solvent is considered as a property apparently related to the molecular conformation. With this “ideal” property as example, the methodological aspects are considered of choosing an analytical expression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6309d4f225bd6162cee9b293e1414640
https://doi.org/10.1023/a:1012306829346
https://doi.org/10.1023/a:1012306829346
Autor:
I. G. Tsygankova, I. B. Golovanov
Publikováno v:
Russian Journal of General Chemistry. 71:712-717
A simple structure-property correlation equation was suggested for estimating the distribution factors of molecules in the octanol-water system. The presence of several polar groups in molecules requires inclusion of additional terms taking into acco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f754090851084ce5e1da92dce375bbaa
https://doi.org/10.1023/a:1012397032555
https://doi.org/10.1023/a:1012397032555