Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Marina A. Zakharko"'
Autor:
Boris S. Morozov, Dr. Siva S. R. Namashivaya, Marina A. Zakharko, Dr. Aleksandr S. Oshchepkov, Prof. Dr. Evgeny A. Kataev
Publikováno v:
ChemistryOpen, Vol 9, Iss 2, Pp 171-175 (2020)
Abstract A new amido−amine cage receptor, which combines 1,8‐anthracene diacarboxamide subunit and a polyammonium azamacrocycle, is reported. Bearing both the hydrogen bond donor and the acceptor binding sites, the receptor is able to bind phosph
Externí odkaz:
https://doaj.org/article/2404cc9ba3404c0d84dbdf361b76cb39
Autor:
M. A. Grin, Andrey F. Mironov, Pavel A. Panchenko, Valentine G. Nenajdenko, Danil P. Zarezin, Olga A. Fedorova, Dmitriy A. Pritmov, Marina A. Zakharko
Publikováno v:
Russian Chemical Bulletin. 69:1169-1178
New conjugates of fluorophore based on 3,4-dimethoxy-4-styryl-1,8-naphthalimide and photosensitizer bacteriochlorin e differing in the nature of spacer fragments were synthesized and their spectral-luminescent properties were studied. The conjugates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a2da8772063b98008fbc73b49da070d
https://doi.org/10.1007/s11172-020-2885-5
https://doi.org/10.1007/s11172-020-2885-5
Publikováno v:
Mendeleev Communications. 30:332-335
New 4-methoxy-1,8-naphthalimide derivative equipped with bis(o-aminophenoxy)ethane-N,N,N',N'-tetraacetate receptor moiety at the imide nitrogen atom showed a fluorescent response to Ca2+ cations due to the formation of complexes of 1:1 ligand–metal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbba1f8193b0ad558342fcf1d347860e
https://doi.org/10.1016/j.mencom.2020.05.024
https://doi.org/10.1016/j.mencom.2020.05.024
Publikováno v:
Mendeleev Communications. 30:55-58
New 4-methoxy-1,8-naphthalimide derivative containing a salicylideneamino receptor group at the imide nitrogen atom demonstrated selective fluorescent response to Zn2+ cations due to the formation of 1: 2 and 2: 1 ligand–metal complexes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fc3e62b8aa2b7c01db595e71e714241
https://doi.org/10.1016/j.mencom.2020.01.018
https://doi.org/10.1016/j.mencom.2020.01.018
Publikováno v:
BIOTECHNOLOGY: STATE OF THE ART AND PERSPECTIVES. :92-94
In this work, hybrid magnetite-gold nanoparticles have been obtained, which have high contrast characteristics in magnetic resonance imaging, as well as opportunities for use in photodynamic therapy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::389f7b32dc3add1723a8810f7c64af24
https://doi.org/10.37747/2312-640x-2020-18-92-94
https://doi.org/10.37747/2312-640x-2020-18-92-94
Autor:
Evgeny A. Kataev, Siva S. R. Namashivaya, Aleksandr S. Oshchepkov, Marina A. Zakharko, Boris S. Morozov
Publikováno v:
ChemistryOpen, Vol 9, Iss 2, Pp 99-99 (2020)
ChemistryOpen, Vol 9, Iss 2, Pp 171-175 (2020)
ChemistryOpen
ChemistryOpen, Vol 9, Iss 2, Pp 171-175 (2020)
ChemistryOpen
A new amido−amine cage receptor, which combines 1,8‐anthracene diacarboxamide subunit and a polyammonium azamacrocycle, is reported. Bearing both the hydrogen bond donor and the acceptor binding sites, the receptor is able to bind phosphate selec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb682c021efd5ede7e2256b0e6d6c9b3
https://opus4.kobv.de/opus4-fau/files/15353/OPEN_OPEN201900309.pdf
https://opus4.kobv.de/opus4-fau/files/15353/OPEN_OPEN201900309.pdf
Autor:
Aleksandr S. Oshchepkov, Marina A. Zakharko, Siva S. R. Namashivaya, Boris S. Morozov, Evgeny A. Kataev
The Front Cover shows the authors’ association of fluorescence anion sensing with pearl hunting – the activity of recovering pearls from wild molluscs. In the presented work, the group of Kataev has developed a new water‐soluble amido‐amine a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a2f52816e80eed6901a10954f676bbb
https://europepmc.org/articles/PMC6996564/
https://europepmc.org/articles/PMC6996564/
Autor:
María González-Béjar, Julia Pérez-Prieto, Laura Francés-Soriano, José Manuel García-Verdugo, Dmitriy A. Pritmov, Andrey F. Mironov, Olga A. Fedorova, Marina A. Zakharko, M. A. Grin, Vicente Herranz-Pérez, Pavel A. Panchenko
Publikováno v:
Chemistry of Materials. 30:3677-3682
Theranostic upconversion nanoparticles (UCNPs) are ideal candidates for personalized medicine. We present a smart, easy-to-prepare nanohybrid (NH) suitable for NIR-theragnosis and imaging tracking without triggering therapy simultaneously. The photop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9be8ee91e73a214aed993fe47dff6c8
https://doi.org/10.1021/acs.chemmater.8b00276
https://doi.org/10.1021/acs.chemmater.8b00276
Autor:
Dmitriy A. Pritmov, Pavel A. Panchenko, Andrey F. Mironov, Yuri V. Fedorov, Marina A. Zakharko, Gediminas Jonusauskas, Mikhail A. Grin, Olga A. Fedorova
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry
Journal of Photochemistry and Photobiology A: Chemistry, Elsevier, 2019, 390, pp.112338. ⟨10.1016/j.jphotochem.2019.112338⟩
Journal of Photochemistry and Photobiology A: Chemistry, Elsevier, 2019, 390, pp.112338. ⟨10.1016/j.jphotochem.2019.112338⟩
Conjugation of 4-pyrazolinyl-1,8-naphthalimide and propargyl-152,173-dimethoxy-131-amide of bacteriochlorin e by the oligo(ethylene glycol) linker resulted in the dual function system comprising the modalities of a photosensitizer and a fluorescence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58151cc68190cc533f7e9aef985150e8
https://hal.archives-ouvertes.fr/hal-02423692/file/GJ_JPhotochemPhotobiol_2019.pdf
https://hal.archives-ouvertes.fr/hal-02423692/file/GJ_JPhotochemPhotobiol_2019.pdf
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