Zobrazeno 1 - 10
of 125
pro vyhledávání: '"László Lázár"'
Publikováno v:
ARKIVOC, Vol 2016, Iss 6, Pp 247-258 (2017)
Externí odkaz:
https://doaj.org/article/0a87a59ded044b598fff979e4ad806d0
Autor:
István Ilisz, Nóra Grecsó, Aleksandra Misicka, Dagmara Tymecka, László Lázár, Wolfgang Lindner, Antal Péter
Publikováno v:
Molecules, Vol 20, Iss 1, Pp 70-87 (2014)
The enantiomers of twelve unusual β2- and β3-homoamino acids containing the same side-chains were separated on chiral stationary phases containing a quinine- or quinidine-based zwitterionic ion-exchanger as chiral selector. The effects of the mobil
Externí odkaz:
https://doaj.org/article/44a25cce17654b87951ec97e8a01f6f9
Publikováno v:
ARKIVOC, Vol 2012, Iss 5, Pp 312-325 (2012)
Externí odkaz:
https://doaj.org/article/67e3a1aa839640a9beaca825ef23ddc9
Publikováno v:
ARKIVOC, Vol 2012, Iss 5, Pp 244-264 (2012)
Externí odkaz:
https://doaj.org/article/262403ff1a724775a1aeeaa003ea7169
Publikováno v:
ARKIVOC, Vol 2004, Iss 7, Pp 196-207 (2004)
Externí odkaz:
https://doaj.org/article/75ed8be7944341e09f606540b46c692d
Autor:
Zita Zalán, Ferenc Bogár, Ferenc Fülöp, Lívia Fülöp, Csaba Tömböly, László Lázár, Botond Penke, Márta Palkó, Szabolcs Dvorácskó
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 8112, p 8112 (2021)
International Journal of Molecular Sciences
Volume 22
Issue 15
International Journal of Molecular Sciences
Volume 22
Issue 15
Sigma-1 receptor (S1R) is an intracellular, multi-functional, ligand operated protein that also acts as a chaperone. It is considered as a pluripotent drug target in several pathologies. The publication of agonist and antagonist bound receptor struct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::859ec8eb660e8a7583d54e59d85987a3
https://www.mdpi.com/1422-0067/22/15/8112
https://www.mdpi.com/1422-0067/22/15/8112
Autor:
László Lázár, László Somsák, Marietta Tóth, Éva Juhász-Tóth, Éva Bokor, Sándor Kun, László Juhász
Publikováno v:
Pure and Applied Chemistry. 91:1159-1175
Glycomimetics are compounds that resemble carbohydrate molecules in their chemical structure and/or biological effect. A large variety of compounds can be designed and synthesized to get glycomimetics, however, C-glycosyl derivatives represent one of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74e969b3198d3286476fd4175741022a
https://doi.org/10.1515/pac-2019-0208
https://doi.org/10.1515/pac-2019-0208
Publikováno v:
Carbohydrate Research. 470:8-12
Phenyl 2,3,6,2′,3′,6′-hexa-O-acetyl-4′-S-acetyl-1,4,4′-trithio-β- d -maltoside and its tri-, tetra- and pentasaccharide homologues were prepared by completely regio- and stereoselective photoinitiated thiol-ene coupling reactions of 2-acet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a493eb2c3b4534a7551dbbf8edc4470f
https://doi.org/10.1016/j.carres.2018.09.005
https://doi.org/10.1016/j.carres.2018.09.005
Autor:
Eszter Csibi-Kuti, László Lázár
Publikováno v:
Vezetéstudomány / Budapest Management Review. 48:46-58
Olyan kort élünk, amikor a felelősség fogalma áthatja a közéletet és szervezeteink világát; keressük, azonosítjuk, vágyjuk, hiányoljuk, számon kérjük, tulajdonítjuk, vállaljuk, vitatjuk, tagadjuk egyéni és közösségi szinteken
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82b5ad195f4cea46e53ed97b5bcdb590
https://doi.org/10.14267/veztud.2017.09.05
https://doi.org/10.14267/veztud.2017.09.05
Publikováno v:
New Journal of Chemistry. 41:1284-1292
Free-radical hydrothiolation of O-peracylated 1-C-(carbamoyl-, methoxycarbonyl- and cyano) substituted glycals with a range of sugar derived thiols gave the corresponding β-manno type 3-deoxy-3-S-disaccharides with full regio- and stereoselectivity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::211d8a90b0e75bafbc08cdd951067523
https://doi.org/10.1039/c6nj03751h
https://doi.org/10.1039/c6nj03751h