Zobrazeno 1 - 10
of 98
pro vyhledávání: '"A. V. Samet"'
Autor:
Dmitry V. Tsyganov, Alexander V. Samet, Eugenia A. Silyanova, Vladimir I. Ushkarov, Alexander E. Varakutin, Natalia B. Chernysheva, Roman N. Chuprov-Netochin, Andrey A. Khomutov, Anna S. Volkova, Sergey V. Leonov, Marina N. Semenova, Victor V. Semenov
Publikováno v:
ACS Omega, Vol 7, Iss 4, Pp 3369-3383 (2022)
Externí odkaz:
https://doaj.org/article/16dffba4f2bf43e6a6b374523bb38672
Autor:
Daniil A. Rusanov, Samah Mutasim Alfadul, Ekaterina Yu. Portnyagina, Eugenia A. Silyanova, Nikita A. Kuznetsov, Kirill E. Podpovetny, Alexander V. Samet, Victor V. Semenov, Maria V. Babak
Publikováno v:
ChemBioChem.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2eedb3797b1b038a334fbfaf12b6265
https://doi.org/10.1002/cbic.202300161
https://doi.org/10.1002/cbic.202300161
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:944-948
A method for the preparation of chromeno[3,4-b]pyrrol-4(3H)-ones via the synthesis of the corresponding 3-arylpyrrole-2-carboxylates from pseudonitrosites by the Barton–Zard reaction was developed. As a result of selective O-demethylation upon expo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b003c5bf2eefa93d89912ec70cd78f6
https://doi.org/10.1007/s10593-021-03004-3
https://doi.org/10.1007/s10593-021-03004-3
Publikováno v:
Russian Chemical Bulletin. 70:498-509
A series of 3,4-diarylpyrrole-2-carboxamides was synthesized using the Barton—Zard reaction of nitrostilbenes with ethyl isocyanoacetate in the key stage. The antiproliferative properties of these compounds were studied on a sea urchin embryo model
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::159e1d22888f94fcd8212515196674db
https://doi.org/10.1007/s11172-021-3115-5
https://doi.org/10.1007/s11172-021-3115-5
Publikováno v:
The Journal of organic chemistry. 87(9)
The 1,3-dipolar cycloaddition reaction of isoquinolinium ylides to nitrostilbenes provides an approach to 1,2-diarylpyrrolo[2,1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d10cbb4673911c3eee88649d8bb0f6f
https://pubmed.ncbi.nlm.nih.gov/35467869
https://pubmed.ncbi.nlm.nih.gov/35467869
Autor:
Victor V. Semenov, Victor N. Khrustalev, Alexander V. Samet, Eugenia A. Silyanova, Lev K. Salamandra
Publikováno v:
European Journal of Organic Chemistry. 2020:2093-2100
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cbb00ae924fde429d5b8b783219ba52
https://doi.org/10.1002/ejoc.202000099
https://doi.org/10.1002/ejoc.202000099
Autor:
Leonid D. Konyushkin, Delphine Gorses, Alexander V. Samet, Victor V. Semenov, Marina N. Semenova, Arkady A. Dudinov, Evgenii N Khodot, Mikhail M. Krayushkin, Eugenia A. Silyanova, Alexei S. Karpov, Boris V. Lichitsky, Thomas Radimerski, Alex S. Kiselyov, Andrey N. Komogortsev
Publikováno v:
ACS Combinatorial Science. 21:805-816
1,3-Substituted pyrazolo[3,4-b]pyridinones 11-18 were synthesized by a three-component condensation of Meldrum's acid with aryl aldehydes and 1,3-substituted 5-aminopyrazoles. Their biological activity was evaluated using the in vivo phenotypic sea u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa5709419948b56c9ec086d82231691b
https://doi.org/10.1021/acscombsci.9b00135
https://doi.org/10.1021/acscombsci.9b00135
Autor:
Andrey B. Myshlyavtsev, Daniil A. Rusanov, V. V. Rusak, Marina N. Semenova, Victor V. Semenov, Eduard M Chartov, Alexander V. Samet, Oksana G Shevchenko
Publikováno v:
Journal of Natural Products. 82:1451-1458
Free-radical-scavenging capacity antioxidant and membrane-protective properties of natural and related synthetic allylpolyalkoxybenzenes with different numbers of alkoxy/methoxy groups in the aromatic ring were evaluated using several in vitro models
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72ea22bb055629403edafc77e52d4987
https://doi.org/10.1021/acs.jnatprod.8b00878
https://doi.org/10.1021/acs.jnatprod.8b00878
Publikováno v:
Russian Chemical Bulletin. 67:2316-2319
Barton-Zard reaction of nitrostilbenes with ethyl isocyanoacetate carried out in EtOH in the presence of K2CO3 allowed us to minimize the formation of side products and to obtain 3,4-diarylpyrrole-2-carboxylates in high yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ceca6c38d3e4b6be2a17f8a742319752
https://doi.org/10.1007/s11172-018-2375-1
https://doi.org/10.1007/s11172-018-2375-1
Autor:
Dmitry V. Demchuk, Alexander E. Varakutin, Anna S. Maksimenko, Alex S. Kiselyov, N. B. Chernysheva, Marina N. Semenova, V. P. Kislyi, Leonid D. Konyushkin, Eugenia A. Silyanova, Mikhail M. Raihstat, Victor V. Semenov, Dmitry V. Tsyganov, Alexander V. Samet
Publikováno v:
ACS Combinatorial Science. 20:700-721
A series of both novel and reported combretastatin analogues, including diarylpyrazoles, -isoxazoles, -1,2,3-triazoles, and -pyrroles, were synthesized via improved protocols to evaluate their antimitotic antitubulin activity using in vivo sea urchin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9201a126c9cf575c8c1bfb403f8a709
https://doi.org/10.1021/acscombsci.8b00113
https://doi.org/10.1021/acscombsci.8b00113