Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Liliya V. Frolova"'
Autor:
Dmitrii A. Aksenov, Alexander V. Aksenov, Lidiya A. Prityko, Nicolai A. Aksenov, Liliya V. Frolova, Michael Rubin
Publikováno v:
Molbank, Vol 2022, Iss 1, p M1307 (2021)
2-Aryl-2-(3-indolyl)acetohydroxamic acids demonstrate promising antitumor activity, but quickly metabolize in vivo via glucuronidation of hydroxamic acid residue. In an attempt to improve their pharmacokinetics, methyl esters were synthesized via a n
Externí odkaz:
https://doaj.org/article/e62b66c4a526404f832ede9d81419362
Publikováno v:
Solar Energy. 208:312-320
This study examined the use of natural dyes extracted from New Mexico prickly pear (Opuntia phaeacantha) and New Mexico mulberry (Morus rubra) in dye-sensitized solar cells (DSSC). The main pigments betalain (betanin plus betaxanthin molecules) in pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4025e16dcdafae3ecd3b3959c7db684d
https://doi.org/10.1016/j.solener.2020.08.006
https://doi.org/10.1016/j.solener.2020.08.006
Publikováno v:
Future Microbiol
Aim: The current report describes the discovery of indole derivatives that synergize with standard antibiotics. Materials & methods: The antibacterial activities were determined using an optimized time–kill method, while viability of mammalian cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a28713fb6c209dc7de187d2211f397d7
https://doi.org/10.2217/fmb-2019-0094
https://doi.org/10.2217/fmb-2019-0094
Publikováno v:
Nanotheranostics
The hydrophobicity and high potency of many therapeutic agents makes them difficult to use effectively in clinical practice. This work focuses on conjugating phospholipid tails (2T) onto podophyllotoxin (P) and its analogue (N) using a linker and cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f371119bdc39705a3952185bd6b57772
http://europepmc.org/articles/PMC6940203
http://europepmc.org/articles/PMC6940203
Autor:
Ruwini D. Rajapaksha, Danielle N. Turner, Jeffrey A. Altig, Mahinda I. Ranasinghe, Jade Vigil, Snezna Rogelj, Liliya V. Frolova
Publikováno v:
J Photochem Photobiol A Chem
The structural dependence of the photo-physical properties of substituted 2,3-distyryl (23DSI) indoles were studied using several spectroscopic techniques including steady-state UV-VIS spectroscopy, steady-state fluorescence spectroscopy, steady-stat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1554ae1ad10bab91cc243bde48c9f5fe
https://doi.org/10.1016/j.jphotochem.2019.03.005
https://doi.org/10.1016/j.jphotochem.2019.03.005
Autor:
Brian M. Kowalski, Liliya V. Frolova, Nikolai G. Kalugin, Alexey Serov, Kateryna Artyushkova, Lindsay Candelaria
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Scientific Reports
Scientific Reports
Carbon-based stationary phases for chromatographic separation have been commercially available since the 1980s. Porous graphitic carbon liquid chromatography columns are known to be highly resistant to aggressive mobile phases and extreme pH values o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc64a4bfefe2f2b247eb7e364669b984
http://link.springer.com/article/10.1038/s41598-018-33075-w
http://link.springer.com/article/10.1038/s41598-018-33075-w
Autor:
Liliya V. Frolova, Ruwini D. Rajapaksha, Cody Champion, Matthias T. Banet, Mahinda I. Ranasinghe, Pabitra Choudhury, Snezna Rogelj
Publikováno v:
The Journal of Physical Chemistry A. 122:937-945
Optical properties and fluorescence decay dynamics of a photoactive indole based antibacterial chromophore system, 2,3-distyrylindole (23DSI), were investigated using various spectroscopic characterization techniques. Experimental studies were done b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fa8897b8de05e3bbeb717df8838b243
https://doi.org/10.1021/acs.jpca.7b09638
https://doi.org/10.1021/acs.jpca.7b09638
Autor:
Véronique Mathieu, Xiaojie Yu, Snezna Rogelj, Marco Masi, Annelise De Carvalho, Alessio Cimmino, Alexander Kornienko, Liliya V. Frolova, Robert Kiss, Antonio Evidente, Alexander Pertsemlidis
Publikováno v:
Fitoterapia. 102:41-48
A new alkaloid, belonging to the pretazettine group of Amaryllidaceae alkaloids, was isolated from dried bulbs of Narcissus jonquilla quail and named jonquailine. Its structure, including the absolute configuration, was elucidated using various NMR,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb6bcf0421eeac05a226b5b216c9041d
https://doi.org/10.1016/j.fitote.2015.01.009
https://doi.org/10.1016/j.fitote.2015.01.009
Autor:
Elvira S. Batyeva, E. K. Badeeva, Snezna Rogelj, Angelo Santomenna, Oleg G. Sinyashin, Liliya V. Frolova, Aidar T. Gubaidullin
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 191:405-410
A new reaction of elemental phosphorus (P4) with elemental sulfur and 1,3-propylene glycol in the presence of different amines has been investigated. Ammonium salts of O,O′- alkylenedithiophosphoric acids have been observed as main products of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ef366d29cc21c5e8159a41e8762a316
https://doi.org/10.1080/10426507.2015.1091828
https://doi.org/10.1080/10426507.2015.1091828
Autor:
Ramesh Dasari, Liliya V. Frolova, Sarah K. Frail, Ernest Hamel, R. Matthew Hill, Derek C. Medellin, Stephen C. Pelly, Qiong Zhou, Ruoli Bai, Steven J. Ontiveros, Tania Betancourt, Alexander Kornienko, Robert Scott, Snezna Rogelj, Charles B. Shuster, Willem A. L. van Otterlo, Daniel V. LaBarbera
Publikováno v:
Journal of Medicinal Chemistry. 59:480-485
Docking studies of tubulin-targeting C2-substituted 7-deazahypoxanthine analogues of marine alkaloid rigidins led to the design and synthesis of compounds containing linear C2-substituents. The C2-alkynyl analogue was found to have double- to single-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09b8308963634103599fc6bb4441f2cb
https://doi.org/10.1021/acs.jmedchem.5b01426
https://doi.org/10.1021/acs.jmedchem.5b01426