Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Christos Mitsos"'
Autor:
Stella Manta, Dimitri Komiotis, John K. Gallos, Christos Mitsos, Ioannis Papanastasiou, Nikolaos Kollatos, Georgia-Anna Chatzieffraimidi
Publikováno v:
Mini-Reviews in Medicinal Chemistry. 20:818-830
Pyrrole is a very important pharmacophoric moiety. It has been widely incorporated into the skeleton of antitumor, anti-inflammatory, antibacterial, antioxidant and antifungal active substances. Access to this key heterocycle by diverse routes is par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14dd32dd4524f0a22207ec3e99274281
https://doi.org/10.2174/1389557520666200103123114
https://doi.org/10.2174/1389557520666200103123114
Autor:
Graciela Andrei, Dimitri Komiotis, Niki Tzioumaki, Christos Mitsos, Tania Alexouli, Aggeliki Panagiotopoulou, Dominique Schols, Nikolaos Kollatos, Stella Manta, Christos Giannakas
Background: Nucleoside analogues are well-known antitumor, antiviral, and chemotherapeutic agents. Alterations on both their sugar and the heterocyclic parts may lead to significant changes in the spectrum of their biological activity and the degree
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::732a2dde1ec7d1b3aa684f00a9c21d5a
https://lirias.kuleuven.be/handle/123456789/649263
https://lirias.kuleuven.be/handle/123456789/649263
Autor:
Dominique Schols, Ioannis Papanastasiou, Aggeliki Panagiotopoulou, Andrew Tsotinis, Niki Tzioumaki, Pelagia Andrea, Dimitri Komiotis, Stella Manta, Nikolaos Kollatos, Christos Mitsos, Marili Margaritouli
Publikováno v:
Current Microwave Chemistry. 5:23-31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::888616bbe3f30d3b0763a84e709624fc
https://doi.org/10.2174/2213335605666180221155915
https://doi.org/10.2174/2213335605666180221155915
Publikováno v:
Chemical and Pharmaceutical Bulletin. 48:211-214
4-Oxo-3-quinolinecarboxylic acid derivatives constitute a class of heterocyclic compounds of great importance in pharmaceutical science. The group of antibacterial agents collectivelly known as ‘quinolones,’ comprises quinoline and 1,8napthyridin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d3b3ca34a3a205d9ff3a827f219af3e
https://doi.org/10.1248/cpb.48.211
https://doi.org/10.1248/cpb.48.211
Publikováno v:
Journal of Heterocyclic Chemistry. 36:881-887
3-(Hydrazonoethyl)quinolinones 6–11, 13 and 3-(hydroxyiminoethyl)quinolinones 14, 15 are prepared by a condensation reaction of 3-acetylquinolinones 4, 5 with a variety of 1,2-(bis)nucleophiles. The structures of the isolated compounds have been el
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e940c38d0187f7d13771b11c18a9919d
https://doi.org/10.1002/jhet.5570360409
https://doi.org/10.1002/jhet.5570360409
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99fddb18fb5b77a89e432b0d84618ad1
https://doi.org/10.1002/chin.199943142
https://doi.org/10.1002/chin.199943142
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::705464f90eb143b1c8dee1833e1f3f85
https://doi.org/10.1002/chin.199942155
https://doi.org/10.1002/chin.199942155
Publikováno v:
ChemInform. 31
3-(Hydrazonoethyl)quinolinones 6–11, 13 and 3-(hydroxyiminoethyl)quinolinones 14, 15 are prepared by a condensation reaction of 3-acetylquinolinones 4, 5 with a variety of 1,2-(bis)nucleophiles. The structures of the isolated compounds have been el
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6d5cb1b9acd42e0dfbb630d85de9fc7
https://doi.org/10.1002/chin.200004160
https://doi.org/10.1002/chin.200004160
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d6dcbfe08ce5342dc777e2880d94667
https://doi.org/10.1002/chin.200029116
https://doi.org/10.1002/chin.200029116
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61c8b280d1175f5ce5b1c7cb19102131
https://doi.org/10.1002/chin.200140141
https://doi.org/10.1002/chin.200140141