Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Konstantina C Fylaktakidou"'
Autor:
Evanthia Kontomina, Vasiliki Garefalaki, Konstantina C Fylaktakidou, Dorothea Evmorfidou, Athina Eleftheraki, Marina Avramidou, Karen Udoh, Maria Panopoulou, Tamás Felföldi, Károly Márialigeti, Giannoulis Fakis, Sotiria Boukouvala
Publikováno v:
PLoS ONE, Vol 17, Iss 7, p e0271125 (2022)
Bacteria employ secondary metabolism to combat competitors, and xenobiotic metabolism to survive their chemical environment. This project has aimed to introduce a bacterial collection enabling comprehensive comparative investigations of those functio
Externí odkaz:
https://doaj.org/article/16b2c39ee3294e9592c8e4464c445009
Autor:
Polinikis Paisidis, Maroula G. Kokotou, Antigoni Kotali, George Psomas, Konstantina C. Fylaktakidou
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 18, p 9842 (2024)
Anthranilic acids, salicylaldehydes and arylboronic acids reacted in EtOH/H2O (1/3) at 150 °C under microwave irradiation for 1 h to give, in excellent yields and purity, twenty-three bridgehead bicyclo[4.4.0]boron heterocycles via one-pot, three-co
Externí odkaz:
https://doaj.org/article/397a67fd3ec7466393584b6664af99dc
Autor:
Achilleas Mitrakas, Maria-Eleni K. Stathopoulou, Chrysoula Mikra, Chrystalla Konstantinou, Stergios Rizos, Stella Malichetoudi, Alexandros E. Koumbis, Maria Koffa, Konstantina C. Fylaktakidou
Publikováno v:
Molecules, Vol 29, Iss 3, p 647 (2024)
Diacylhydrazine bridged anthranilic acids with aryl and heteroaryl domains have been synthesized as the open flexible scaffold of arylamide quinazolinones in order to investigate flexibility versus rigidity towards DNA photocleavage and sensitivity.
Externí odkaz:
https://doaj.org/article/8645a99551624a4290dddc738daf6dcf
Autor:
Anastasios Panagopoulos, Konstantina Alipranti, Kyriaki Mylona, Polinikis Paisidis, Stergios Rizos, Alexandros E. Koumbis, Emmanouil Roditakis, Konstantina C. Fylaktakidou
Publikováno v:
DNA; Volume 3; Issue 2; Pages: 85-100
The DNA photocleavage effect of halogenated O-carbamoyl derivatives of 4-MeO-benzamidoxime under UVB and UVA irradiation was studied in order to identify the nature, position, and number of halogens on the carbamoyl moiety that ensure photoactivity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ecd3b787e80e34fc1bf9e86e245b1fe
https://doi.org/10.3390/dna3020006
https://doi.org/10.3390/dna3020006
Autor:
Chrisoula Kakoulidou, Christos T. Chasapis, Antonios G. Hatzidimitriou, Konstantina C. Fylaktakidou, George Psomas
Publikováno v:
Dalton Transactions. 51:16688-16705
Six transition metal(ii) complexes with halogenated quinazoline derivatives as ligands were characterized and evaluated for interaction with calf-thymus DNA, photocleavage of plasmid-DNA, affinity for bovine serum albumin, and antioxidant activity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28f30d4e781902d6928b7d491c97e350
https://doi.org/10.1039/d2dt02622h
https://doi.org/10.1039/d2dt02622h
Autor:
Chrysoula Mikra, Achilleas Mitrakas, Virginia Ghizzani, Katerina R. Katsani, Maria Koffa, Michael Koukourakis, George Psomas, Stefano Protti, Maurizio Fagnoni, Konstantina C. Fylaktakidou
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 3; Pages: 1834
A set of arylazo sulfones, known to undergo N–S bond cleavage upon light exposure, has been synthesized, and their activity in the dark and upon irradiation towards DNA has been investigated. Their interaction with calf-thymus DNA has been examined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6954742f4a3bf9bdd9b0128662551ee4
Autor:
Panayiotis C. Varras, Konstantina C. Fylaktakidou, Konstantinos Dafnopoulos, Nikolaos-Panagiotis Andreou, George Psomas, Panagiotis S. Gritzapis, Zisis V. Peitsinis, Alexandros E. Koumbis, Katerina R. Katsani
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 337-350 (2020)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
A number of p-pyridinyl oxime carbamate derivatives were prepared upon the reaction of the corresponding oximes with isocyanates. These novel compounds reacted photochemically in the presence of supercoiled plasmid DNA. Structure–activity relations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee0f43fb7ab9b295e7da626de724f5db
https://doaj.org/article/a8d3b1eb0f704eeda37ccb1c74645332
https://doaj.org/article/a8d3b1eb0f704eeda37ccb1c74645332
Autor:
Chrysoula Mikra, Maria Bairaktari, Marina-Theodora Petridi, Anastasia Detsi, Konstantina C. Fylaktakidou
Publikováno v:
Processes; Volume 10; Issue 2; Pages: 384
Eleven 3-amino-2-methyl-quinazolin-4(3H)-ones have been synthesized, in good to excellent yields, via their corresponding benzoxazinones using an efficient tandem microwave-assisted green process. Representative acetamides have been thermally derived
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::819dae89aced8f0ee48281eca782b0f5
Autor:
Evanthia Kontomina, Vasiliki Garefalaki, Konstantina C. Fylaktakidou, Dorothea Evmorfidou, Athina Eleftheraki, Marina Avramidou, Karen Udoh, Maria Panopoulou, Tamás Felföldi, Károly Márialigeti, Giannoulis Fakis, Sotiria Boukouvala
Publikováno v:
PloS one. 17(7)
Bacteria employ secondary metabolism to combat competitors, and xenobiotic metabolism to survive their chemical environment. This project has aimed to introduce a bacterial collection enabling comprehensive comparative investigations of those functio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d5b07e52eb5f462643da0e06322e0f5
https://pubmed.ncbi.nlm.nih.gov/35834592
https://pubmed.ncbi.nlm.nih.gov/35834592
Autor:
Chrysoula Mikra, Zoi Melissari, Maroula G. Kokotou, Panagiotis Gritzapis, Konstantina C. Fylaktakidou
Publikováno v:
Sustainable Chemistry and Pharmacy. 29:100772
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22b1d69ea863ad37e95ffe5a9ea2a68f
https://doi.org/10.1016/j.scp.2022.100772
https://doi.org/10.1016/j.scp.2022.100772