Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Zinaida M, Kaskova"'
Autor:
Zinaida M. Kaskova, Anastasia A. Andrianova, Aleksandra S. Tsarkova, Yulia V. Nelyubina, Nadezhda S. Baleeva, Yaroslav V. Bolt
Publikováno v:
Synlett. 32:2059-2062
We report a simple two-step method for the synthesis of a novel highly fluorescent benzothiophene-based dye comprising five fused rings and exhibiting a large Stokes shift (Δλ = 152 nm or Δν = 5482 cm–1 in ethanol). Structural features of the o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5964bb33193c23fbd52c6d2c1336033
https://doi.org/10.1055/s-0040-1720925
https://doi.org/10.1055/s-0040-1720925
Autor:
Eugene S. Vysotski, Ilia V. Yampolsky, Aleksandra S. Tsarkova, Konstantin S. Mineev, Zinaida M. Kaskova, Renata I Zagitova, Ludmila P. Burakova, Sergey I. Kovalchuk, Valentin N. Petushkov, Maria S Lyakhovich
Publikováno v:
Organic Letters. 23:6846-6849
Ca2+-regulated photoproteins of ctenophores lose bioluminescence activity when exposed to visible light. Little is known about the chemical nature of chromophore photoinactivation. Using a total synthesis strategy, we have established the structures
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12ca3dc4665a782d9cecb2ae325a335d
https://doi.org/10.1021/acs.orglett.1c02410
https://doi.org/10.1021/acs.orglett.1c02410
Autor:
Zinaida M. Kaskova, Maxim A. Dubinnyi, Natalia S. Rodionova, Valentin N. Petushkov, Sergey I. Kovalchuk, Igor Ivanov
Publikováno v:
ChemistrySelect. 5:13155-13159
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f5471a8e211321e1bcb9f5bfadcaf1d
https://doi.org/10.1002/slct.202003075
https://doi.org/10.1002/slct.202003075
Publikováno v:
Acta Naturae
Optoanalytical methods based on using genetically encoded bioluminescent enzymes,luciferases, allow one to obtain highly sensitive signals, are non-invasive, and require no external irradiation. Bioluminescence is based on the chemical reaction of ox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06c6fe275d6d0693eefcd1a13e450528
http://europepmc.org/articles/PMC7385095
http://europepmc.org/articles/PMC7385095
Autor:
Ludmila P, Burakova, Maria S, Lyakhovich, Konstantin S, Mineev, Valentin N, Petushkov, Renata I, Zagitova, Aleksandra S, Tsarkova, Sergey I, Kovalchuk, Ilia V, Yampolsky, Eugene S, Vysotski, Zinaida M, Kaskova
Publikováno v:
Organic letters. 23(17)
Ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2c8a5a7306cddc228e5c5da3be4843ad
https://pubmed.ncbi.nlm.nih.gov/34416112
https://pubmed.ncbi.nlm.nih.gov/34416112
Autor:
Gleb Bourenkov, Yuichi Oba, Zinaida M. Kaskova, Yulia V. Nelyubina, Yaroslav V. Bolt, Igor E. Eliseev, Igor Ivanov, A A Kotlobay, Aleksandra S. Tsarkova, Elena B. Guglya, Ilia V. Yampolsky, K. V. Purtov, Pavel V. Dorovatovskii, Natalja S. Rodionova, Maxim A. Dubinnyi, Rustam H. Ziganshin, Vadim S. Kublitski, Valentin N. Petushkov, Bruce R. Branchini
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Significance We report the identification and characterization of the small molecule aspects of the Odontosyllis undecimdonta bioluminescence system. The chemical structures of the 4 best-known marine luciferins are as diverse as their phylogenetic d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bb323a9ef9e678df956467c88827449
https://doi.org/10.1073/pnas.1902095116
https://doi.org/10.1073/pnas.1902095116
Publikováno v:
Russian Journal of Bioorganic Chemistry. 45:183-185
Current studies of fungal bioluminescent systems, including the purification of luciferase, require large quantities of the synthetic substrate luciferin available. The existing synthetic method for the luciferin produces low yield of the target mole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e7eebdd8243f06ed7f3dd87224af45a
https://doi.org/10.1134/s106816201902002x
https://doi.org/10.1134/s106816201902002x
Autor:
Alexander S. Arseniev, Dmitrii I. Moskvin, Ilia V. Yampolsky, Yulii Aleksandrovich Labas, Mikhail S. Baranov, Konstantin S. Mineev, Alexander A. Kislukhin, Pavel E. Ivashkin, Zinaida M. Kaskova, Roman Gritсenko, Svetlana G. Postikova
Publikováno v:
Synlett. 28:583-588
Panal is a natural bicyclic cadalane-type sesquiterpenoid with an unusual combination of stereocenters. It was isolated in 1988 as an alleged biosynthetic precursor of luciferin (a light-emitting molecule) in a bioluminescent fungus Panellus stipticu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75362395b8297c74d1e1969cc6a43d2a
https://doi.org/10.1055/s-0036-1588104
https://doi.org/10.1055/s-0036-1588104