Zobrazeno 1 - 10
of 16
pro vyhledávání: '"L. I. Gabrielyan"'
Autor:
L. I. Gabrielyan, A. S. Kabankin
Publikováno v:
Pharmaceutical Chemistry Journal. 40:307-311
Features of the principal component analysis, which can be used to decrease the dimension of the space of initial molecular descriptors in the search for classification rules predicting the activity of new compounds, are considered in application to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::631af9fe5c52eea63bcf9ad9d01edc73
https://doi.org/10.1007/s11094-006-0116-5
https://doi.org/10.1007/s11094-006-0116-5
Autor:
N. V. Ostapchuk, A. S. Kabankin, V. P. Zhestkov, N. E. Pyn'ko, L. A. Radkevich, L. I. Gabrielyan
Publikováno v:
Pharmaceutical Chemistry Journal. 39:191-196
The characteristics of the hepatoprotective activity of some indole derivatives have been determined. The best combinations of substructural molecular descriptors are established, which allows the hepatoprotective activity in the given chemical serie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa52d256f589196d46d86bf6b78d5592
https://doi.org/10.1007/s11094-005-0115-y
https://doi.org/10.1007/s11094-005-0115-y
Autor:
A. S. Kabankin, L. I. Gabrielyan
Publikováno v:
Pharmaceutical Chemistry Journal. 39:135-139
The relationships between structure and hepatoprotector activity in the class of adamantane derivatives were studied by means of linear discriminant analysis with the use of various 2D and 3D descriptors. From the standpoint of predictions based on t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72e51de73165e16bb6f3582a89120606
https://doi.org/10.1007/s11094-005-0102-3
https://doi.org/10.1007/s11094-005-0102-3
Autor:
A. S. Kabankin, L. A. Piruzyan, N. V. Ostapchuk, N. E. Pyn'ko, L. A. Radkevich, L. I. Gabrielyan
Publikováno v:
Pharmaceutical Chemistry Journal. 38:136-142
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b67105193fabeec319e590aeacbd0bb4
https://doi.org/10.1023/b:phac.0000034302.19705.94
https://doi.org/10.1023/b:phac.0000034302.19705.94
Autor:
L. I. Gabrielyan, A. S. Kabankin
Publikováno v:
Pharmaceutical Chemistry Journal. 42:262-264
The AM1 valent approximation version of the self-consistent field (SCF) MO LCAO method was used to calculate the electronic structures of 30 adamantane derivatives and 30 indole derivatives with full optimization of molecular geometry. Linear discrim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc6733182c4232b50d952bc76eaea731
https://doi.org/10.1007/s11094-008-0107-9
https://doi.org/10.1007/s11094-008-0107-9
Autor:
Kabankin, A.1, Radkevich, L.1
Publikováno v:
Pharmaceutical Chemistry Journal. Jul2013, Vol. 47 Issue 4, p181-186. 6p. 4 Charts.
Autor:
Kabankin, A.1, Gabrielyan, L.1
Publikováno v:
Pharmaceutical Chemistry Journal. Jun2006, Vol. 40 Issue 6, p307-311. 5p. 3 Charts.
Autor:
Kabankin, A. S.1, Gabrielyan, L. I.1
Publikováno v:
Pharmaceutical Chemistry Journal. May2008, Vol. 42 Issue 5, p262-264. 3p. 3 Charts.
Publikováno v:
Pharmaceutical Chemistry Journal. Apr2005, Vol. 39 Issue 4, p191-196. 6p.
Autor:
Kabankin, A. S.1, Gabrielyan, L. I.1
Publikováno v:
Pharmaceutical Chemistry Journal. Mar2005, Vol. 39 Issue 3, p135-139. 5p.