Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Katalin E. Szabó"'
Autor:
Ádám Sipos, Eszter Szennyes, Nikolett Éva Hajnal, Sándor Kun, Katalin E. Szabó, Karen Uray, László Somsák, Tibor Docsa, Éva Bokor
Publikováno v:
Pharmaceuticals, Vol 14, Iss 4, p 364 (2021)
A current trend in the quest for new therapies for complex, multifactorial diseases, such as diabetes mellitus (DM), is to find dual or even multi-target inhibitors. In DM, the sodium dependent glucose cotransporter 2 (SGLT2) in the kidneys and the g
Externí odkaz:
https://doaj.org/article/123aa2e339ec4bb68099bd3b1990d15b
Publikováno v:
Molecules, Vol 22, Iss 10, p 1760 (2017)
Reactions of O-peracylated C-(1-bromo-β-d-glucopyranosyl)formamides with thioamides furnished the corresponding glucopyranosylidene-spiro-thiazolin-4-one. While O-debenzoylations under a variety of conditions resulted in decomposition, during O-deac
Externí odkaz:
https://doaj.org/article/798f1952c0304e67abeab1655ec4990e
Autor:
Katalin E. Szabó, Efthimios Kyriakis, Anna-Maria G. Psarra, Aikaterini G. Karra, Ádám Sipos, Tibor Docsa, George A. Stravodimos, Elisabeth Katsidou, Vassiliki T. Skamnaki, Panagiota G. V. Liggri, Spyros E. Zographos, Attila Mándi, Sándor Balázs Király, Tibor Kurtán, Demetres D. Leonidas, László Somsák
Publikováno v:
Journal of Medicinal Chemistry. 62:6116-6136
Epimeric series of aryl-substituted glucopyranosylidene-spiro-imidazolinones, an unprecedented new ring system, were synthesized from the corresponding Schiff bases of
Autor:
Éva Bokor, Spyros E. Zographos, Georgios A Stravodimos, Anastassia L. Kantsadi, Tibor Docsa, László Somsák, Andrea Szakács, Efthimios Kyriakis, Theodora G.A. Solovou, Demetres D. Leonidas, Katalin E. Szabó, Csenge Koppány, Pál Gergely, Vassiliki T. Skamnaki
Publikováno v:
Journal of Medicinal Chemistry. 60:9251-9262
Aryl substituted 1-(β-d-glucosaminyl)-1,2,3-triazoles as well as C-β-d-glucosaminyl 1,2,4-triazoles and imidazoles were synthesized and tested as inhibitors against muscle and liver isoforms of glycogen phosphorylase (GP). While the N-β-d-glucosam
Publikováno v:
Tetrahedron. 73:3810-3822
Highly variable synthetic routes were elaborated toward trisubstituted C-glycopyranosyl 1,2,4-triazoles. N-Acyl-thioamide derivatives were obtained by acylation of O-perbenzoylated 2,6-anhydro-d-glycero-d-gulo-heptonothioamide by acid chlorides and o
Publikováno v:
Jelenkori Társadalmi és Gazdasági Folyamatok. 12:141-152
Magyarország területe 9,3 millió hektár, mely az elmúlt 15 év alatt némi változásokon ment keresztül. Cikkünkben ezért megvizsgáltuk a teljes területből a termőterület és a kivett terület változását 1990-től napjainkig, majd ez
Autor:
Jaida Begum, Pál Gergely, Maria C. Kokolaki, Thomas A. Barkas, George A. Stravodimos, Ádám Sipos, Eszter Szennyes, Vassiliki T. Skamnaki, Efthimios Kyriakis, Sándor Kun, Joseph Hayes, Colin Moffatt, Tibor Docsa, László Somsák, Alkistis Gkerdi, Evgenia C.V. Stamati, Katalin E. Szabó, Myrto S. Patraskaki, Demetres D. Leonidas, Éva Bokor
Publikováno v:
European Journal of Medicinal Chemistry
3-(β-d-Glucopyranosyl)-5-substituted-1,2,4-triazoles have been revealed as an effective scaffold for the development of potent glycogen phosphorylase (GP) inhibitors but with the potency very sensitive to the nature of the alkyl/aryl 5-substituent (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b96b7abd646b0be9c9d46e956251529
Publikováno v:
Molecules; Volume 22; Issue 10; Pages: 1760
Molecules, Vol 22, Iss 10, p 1760 (2017)
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules, Vol 22, Iss 10, p 1760 (2017)
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Reactions of O-peracylated C-(1-bromo-β-d-glucopyranosyl)formamides with thioamides furnished the corresponding glucopyranosylidene-spiro-thiazolin-4-one. While O-debenzoylations under a variety of conditions resulted in decomposition, during O-deac
Publikováno v:
Journal of Mass Spectrometry. 48:1276-1280
Publikováno v:
ChemInform. 46
Title compounds (V) and (VIII) are synthesized by oxidative ring closures of amidrazones (IV) or (VII), respectively.