Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Vladislav M Malinnikov"'
Autor:
Konstantin I. Kobrakov, Bogdan I. Ugrak, Leonid M. Kustov, Elena V. Shuvalova, Vladislav M. Malinnikov, Kamran T. Mahmudov, Yulia V. Nelyubina, Kirill N. Lialin, Firudin I. Guseinov
Publikováno v:
Dyes and Pigments. 197:109898
A series of 2-(4-substituted benzoyl)thiazolo[3,2-a]pyridin-4-ium bromides [−OCH3 (1), –H (2), –F (3), −Cl (4)] was obtained by the heterocyclization reaction of the corresponding 2-bromo-1-(4-substituted phenyl)-3,3-diethoxypropan-1-ones wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70db5dc0236fb5ef6c34ec82d82590fe
https://doi.org/10.1016/j.dyepig.2021.109898
https://doi.org/10.1016/j.dyepig.2021.109898
Autor:
Eldar M. Movsumzade, Leonid M. Kustov, Vladislav M. Malinnikov, Oksana M. Lavrova, Mikhail F. Pistsov, Firudin I. Guseinov
Publikováno v:
Mendeleev Communications. 30:674-675
3-Diethoxymethyl-3-hydroxy-3,9-dihydro-2H-benz[4,5]imidazo[2,1-b]thiazol-4-ium salts were synthesized by reaction of chloro oxiranes or isomeric α-chloro ketones with 2-mercaptobenzimidazole. The acetal group of the aforementioned salts undergoes hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77e67c4bae21051afdd839e61f725085
https://doi.org/10.1016/j.mencom.2020.09.041
https://doi.org/10.1016/j.mencom.2020.09.041
Autor:
Pavel A. Ignatov, Pavel A. Panchenko, Svetlana V Lavrushkina, Igor I. Kireev, Vladislav M Malinnikov, Elena K. Beloglazkina, Irina V. Grishina, Sergey S Kovalev, Nikolay V. Zyk, Olga O. Krasnovskaya, Dmitry A. Skvortsov, Vasily M. Gerasimov, Marina A. Zakharko, Olga A. Fedorova, Alexander G. Majouga, Natalia S Dashkova, Gediminas Jonusauskas
Publikováno v:
Bioconjugate Chemistry
Bioconjugate Chemistry, American Chemical Society, 2019, 30 (3), pp.741-750. ⟨10.1021/acs.bioconjchem.8b00885⟩
Bioconjugate Chemistry, American Chemical Society, 2019, 30 (3), pp.741-750. ⟨10.1021/acs.bioconjchem.8b00885⟩
International audience; A novel approach to the synthesis of pH-sensitive prodrugs has been proposed: thiourea drug modification. Resulting prodrugs can release the cytotoxic agent and the biologically active 2-thiohydantoin in the acidic environment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::397611eaa0536cac056ce61dd5ab2de2
https://hal.archives-ouvertes.fr/hal-02404558/file/GJ_acs_bioconjchem_2019.pdf
https://hal.archives-ouvertes.fr/hal-02404558/file/GJ_acs_bioconjchem_2019.pdf
Autor:
Vladislav M Malinnikov, Anna V. Udina, Olga O. Krasnovskaya, Alexander G. Majouga, Mikhail A. Proskurnin, Dmitry A. Skvortsov, Vladimir A. Aladinskiy, Radik R. Shafikov, Nikolay V. Zyk, Elena K. Beloglazkina, Oleg I. Gromov, Dmitriy Guk, Ivan D. Sorokin, Ksenia Tishchenko, Marina Muratova, Yan A. Ivanenkov
Publikováno v:
Journal of inorganic biochemistry. 175
New copper(II) complexes of 2-alkylthio-5-arylmethylene-4H-imidazolin-4-ones: (5Z)-2-(methylsulfanyl)-3-(prop-2-en-1-yl)-5-(pyridin-2-ylmethylidene)-3,5-dihydro-4H-imidazol-4-one) ( 1a ), (5Z,5′Z)-2,2′-(ethan-1,2-diyldisulfanyldiyl)bis(5-(2-pyrid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09d9028ec87fffa9b48689b907794b1f
https://pubmed.ncbi.nlm.nih.gov/28756175
https://pubmed.ncbi.nlm.nih.gov/28756175