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Autor:
Angeliki Sofia Foscolos, Andrew Tsotinis, Martin C. Taylor, John M. Kelly, Ioannis P. Papanastasiou
Publikováno v:
Molbank, Vol 2022, Iss 2, p M1363 (2022)
In this work, we present the synthesis and the anti-trypanosomal activity of the 2-(4-(adamant-1-yl)phenyl)-N-hydroxyarylamides, 1a,b and the 2-(4-(adamant-1-yl)phenoxy)-N-hydroxyacetamide, 1c. The 4-(adamant-1-yl)phenyl- and 4-(adamant-1-yl)phenoxy-
Externí odkaz:
https://doaj.org/article/bbaa0dfd6fef4eb1a6920b434ee35a33
Autor:
Vlachou, Marilena, Kikionis, Stefanos, Siamidi, Angeliki, Tragou, Konstantina, Ioannou, Efstathia, Roussis, Vassilios, Tsotinis, Andrew
Publikováno v:
In Journal of Pharmaceutical Sciences February 2019 108(2):970-976
Autor:
Vlachou, Marilena, Tragou, Konstantina, Siamidi, Angeliki, Kikionis, Stefanos, Chatzianagnostou, Angelos-Leontios, Mitsopoulos, Anastasis, Ioannou, Efstathia, Roussis, Vassilios, Tsotinis, Andrew
Publikováno v:
In Journal of Drug Delivery Science and Technology April 2018 44:41-48
Autor:
Foscolos, Angeliki Sofia1 (AUTHOR) angelique.lumiere@windowslive.com, Tsotinis, Andrew1 (AUTHOR) tsotinis@pharm.uoa.gr, Taylor, Martin C.2 (AUTHOR) martin.taylor@lshtm.ac.uk, Kelly, John M.2 (AUTHOR) john.kelly@lshtm.ac.uk, Papanastasiou, Ioannis P.1 (AUTHOR) papanastasiou@pharm.uoa.gr
Publikováno v:
Molbank. Jun2022, Vol. 2022 Issue 2, pM1363-N.PAG. 8p.
Autor:
Fytas, Christos, Zoidis, Grigoris, Tsotinis, Andrew, Fytas, George, Khan, Mohsin A., Akhtar, Samar, Rahman, Khondaker M., Thurston, David E.
Publikováno v:
In European Journal of Medicinal Chemistry 26 March 2015 93:281-290
Autor:
Marilena Vlachou, Stefanos Kikionis, Angeliki Siamidi, Sotiria Kyriakou, Andrew Tsotinis, Efstathia Ioannou, Vassilios Roussis
Publikováno v:
Pharmaceutics, Vol 11, Iss 9, p 480 (2019)
Furosemide, a chloride channel blocker ordinarily used as a high-ceiling or loop diuretic, is practically insoluble in water and dilute acids. Due to its acidic nature, furosemide is mostly absorbed in the stomach and in the upper small intestine. Ef
Externí odkaz:
https://doaj.org/article/41ff390387bb4d56acd9cd771b3d8c49
Autor:
Andrew Tsotinis, Pandelis A. Afroudakis, Ioannis P. Papanastasiou, Aikaterini Sakellaropoulou, Marina Boniakou, Dimitri Komiotis, Peter J. Garratt, Philippe Delagrange, Alina Bocianowska‐Zbrog, David Sugden
Publikováno v:
ChemMedChem. 17
A series of substituted indolo[2,1-a]isoquinolines and indolo[1,2-a]benzoxazines have been prepared, as melatonin analogues, to investigate the nature of the binding site of the melatonin receptor. Agonist and antagonist potency of all the analogues
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c79af17da8eca9f903e1a23186c04639
https://doi.org/10.1002/cmdc.202200129
https://doi.org/10.1002/cmdc.202200129
Autor:
Patrozou, Eleni, Tsotinis, Andrew
Publikováno v:
Pharmakeftiki; Apr-Jun2023, Vol. 35 Issue 2, p2-5, 4p
Autor:
Varvarigou, Nicole, Megariotis, Grigorios, Leonis, Georgios, Vrontaki, Eleni, Maniati, Antigoni-Margarita, Vlachou, Marilena, Eikosipentaki, Aphrodite, Kompogennitaki, Rodanthi, Papadopoulos, Manthos G., Grdadolnik, Simona Golic, Komiotis, Dimitri, Mavromoustakos, Thomas, Tsotinis, Andrew
Publikováno v:
In Bioorganic & Medicinal Chemistry 1 November 2012 20(21):6276-6284