Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Nataliya S. Vorobyeva"'
Autor:
Stanislav I. Bezzubov, Ekaterina M. Budynina, Andrey A. Akaev, Nataliya S. Vorobyeva, Mikhail Ya. Melnikov, Alexander G. Majouga, Victor G. Desyatkin
Publikováno v:
The Journal of Organic Chemistry. 84:3340-3356
A novel stereocontrolled assembly of spiro[oxindole-3,2'-pyrrolidines] via [3+2]-cycloaddition of donor-acceptor cyclopropanes to electron-poor ketimines, iminooxindoles, was developed. The method allows for efficient employment of common readily ava
Publikováno v:
Proteomics. 20(5-6)
Aging results in various deleterious changes in the human body that may lead to loss of function and the manifestation of chronic diseases. While diseases can generally be reliably diagnosed, the aging process itself requires more sophisticated appro
Autor:
K. A. Toropova, Nataliya S. Vorobyeva, Olga I. Ivashkina, Konstantin V. Anokhin, Anna M. Gruzdeva, M A Roshchina
Publikováno v:
Acta Naturae. 10:37-47
In this study, we describe use of Cre-mediated recombination to obtain a permanent genetic labeling of the brain neuronal networks activated during a new experience in animals. This method utilizes bitransgenic Fos-Cre-eGFP mice in which a green fluo
Autor:
Dmitry A. Skvortsov, A. V. Finko, Yan A. Ivanenkov, Egor A. Dlin, Alexander G. Majouga, G.M. Averochkin, Nataliya S. Vorobyeva, Elena K. Beloglazkina, Nikolay V. Zyk, Victor Koteliansky
Publikováno v:
Tetrahedron Letters. 57:5501-5504
A convenient and efficient catalytic procedure for the selective S-arylation of 2-thioxoimidazolidin-4-ones to give novel S-aryl substituted 2-thiohydantoins under mild reaction conditions using arylboronic acids is described. The anticancer activity
Autor:
Nataliya S. Vorobyeva, Alexey E. Machulkin, Elena K. Beloglazkina, A. V. Trofimenko, Alexander G. Majouga, Victor Koteliansky, Ekaterina V. Deyneka, Alina A. Sofronova, Dmitry S. Bezrukov, Yan A. Ivanenkov, Anastasia V. Aladinskaya, Maria M Puchinina, Alexander S. Malyshev, Grigory K. Riabykh, Anastasia A. Uspenskaya, Nikolay V. Zyk, Dmitry A. Skvortsov, Anastasia S. Garanina
Publikováno v:
Bioorganicmedicinal chemistry letters. 29(10)
Prostate-specific membrane antigen (PSMA), also known as glutamate carboxypeptidase II (GCPII), has recently emerged as a prominent biomarker of prostate cancer (PC) and as an attractive protein trap for drug targeting. At the present time, several d
Publikováno v:
Animal cognition. 22(2)
Applying the classical experimental scheme of training animals with food rewards to discriminate between quantities of visual stimuli, we demonstrated that not only can striped field mice Apodemus agrarius discriminate between clearly distinctive qua
Autor:
Nataliya S. Vorobyeva, Alexander Erofeev, Alexander G. Majouga, Yuri E. Korchev, Christopher J Edwards, M. V. Efremova, Petr V. Gorelkin, A. Alova, Anastasiia S Garanina
Publikováno v:
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-11 (2018)
Scientific Reports, Vol 8, Iss 1, Pp 1-11 (2018)
Iron oxide nanoparticles have attracted a great deal of research interest and have been widely used in bioscience and clinical research including as contrast agents for magnetic resonance imaging, hyperthermia and magnetic field assisted radionuclide
Autor:
A. S. Semkina, Stepan Vodopyanov, V.A. Naumenko, Y.O. Tsareva, Nataliya S. Vorobyeva, Aleksey Nikitin, Anastasiia S Garanina, Vladimir P. Chekhonin, Artem Ilyasov, Maxim A. Abakumov, Alexander G. Majouga, M A Kunin
Publikováno v:
Contrast Media & Molecular Imaging, Vol 2018 (2018)
Contrast Media & Molecular Imaging
Contrast Media & Molecular Imaging
Magnetic resonance imaging (MRI) is a powerful technique for tumor diagnostics. Iron oxide nanoparticles (IONPs) are safe and biocompatible tools that can be used for further enhancing MR tumor contrasting. Although numerous IONPs have been proposed
Autor:
Alexander G. Majouga, Nataliya S. Vorobyeva, Andrey A. Akaev, Mikhail Ya. Melnikov, Ekaterina M. Budynina, Elena V. Villemson
Publikováno v:
The Journal of organic chemistry. 82(11)
A new synthetic approach to biologically relevant spiro[pyrrolidine-3,3′-oxindoles] was developed on the basis of the cascade transformation of 3-(2-azidoethyl)oxindoles via Staudinger/aza-Wittig/Mannich reactions. The parent azides were readily sy