Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Nataliya M. Samoshina"'
Autor:
Irina A. Dotsenko, Qinliang Zhao, Andreas H. Franz, Patrick Batoon, Nataliya M. Samoshina, Vyacheslav V. Samoshin
Publikováno v:
ARKIVOC, Vol 2014, Iss 5, Pp 16-41 (2014)
Externí odkaz:
https://doaj.org/article/58225ca6627e40c7a128b4e52838396c
Autor:
Barbora Brazdova, Andreas H. Franz, Vyacheslav V. Samoshin, Xin Guo, Xin Liu, Nataliya M. Samoshina
Publikováno v:
Pharmaceutics, Vol 3, Iss 3, Pp 379-405 (2011)
Incorporation of a pH-sensitive conformational switch into a lipid structure enables a drastic conformational flip upon protonation that disrupts the liposome membrane and causes rapid release of cargo specifically in areas of increased acidity. pH-s
Externí odkaz:
https://doaj.org/article/4ec9019172cc4160a67f971f6d009779
Publikováno v:
Chemistry and physics of lipids. 210
Recently developed lipids with the trans-2-aminocyclohexanol (TACH) moiety represent unique pH-sensitive conformational switches ("flipids") that can trigger the membrane of liposome-based drug delivery systems at lowered pH as seen in many pathologi
Autor:
Irina A. Dotsenko, Nataliya M. Samoshina, Andrey V. Samoshin, Andreas H. Franz, Vyacheslav V. Samoshin
Publikováno v:
International Journal of Carbohydrate Chemistry. 2014:1-8
Structurally simple 1-thio-β-D-glucopyranosides were synthesized and tested as potential inhibitors toward several fungal glycosidases from Aspergillus oryzae and Penicillium canescens. Significant selective inhibition was observed for α- and β-gl
Autor:
Qinliang Zhao, Andreas H. Franz, Irina A. Dotsenko, Vyacheslav V. Samoshin, Nataliya M. Samoshina, Patrick Batoon
Publikováno v:
ARKIVOC, Vol 2014, Iss 5, Pp 16-41 (2014)
Publikováno v:
Journal of Liposome Research. 22:319-328
A new type of pH-sensitive liposomes (fliposomes) was designed based on the amphiphiles that are able to perform a pH-triggered conformational flip (flipids). This flip disrupts the liposome membrane and causes rapid release of the liposome cargo, sp
Publikováno v:
Tetrahedron. 67:7470-7478
A broad series of novel 5-aryl(alkyl)sulfanyl-1,10-phenanthrolines has been prepared by a new simple procedure: a treatment of the commercially available 5,6-epoxy-5,6-dihydro-1,10-phenanthroline with various thiols in the presence of a base. Other f
Autor:
Andreas H. Franz, Barbora Brazdova, Xin Liu, Nataliya M. Samoshina, Vyacheslav V. Samoshin, Xin Guo
Publikováno v:
Pharmaceutics, Vol 3, Iss 3, Pp 379-405 (2011)
Pharmaceutics; Volume 3; Issue 3; Pages: 379-405
Pharmaceutics
Pharmaceutics; Volume 3; Issue 3; Pages: 379-405
Pharmaceutics
Incorporation of a pH-sensitive conformational switch into a lipid structure enables a drastic conformational flip upon protonation that disrupts the liposome membrane and causes rapid release of cargo specifically in areas of increased acidity. pH-s
Publikováno v:
Biochimica et biophysica acta. 1848(12)
Lipidic amphiphiles equipped with the trans-2-aminocyclohexanol (TACH) moiety are promising pH-sensitive conformational switches (“flipids”) that can trigger a lipid bilayer perturbation in response to increased acidity. Because pH-sensitivity wa
Publikováno v:
Enzyme and Microbial Technology. 36:239-251
A comparative analysis of kinetic data for fungal β-galactosidases has revealed that the ratio of Michaelis constants (MCR) with two substrates (lactose and o / p -nitrophenyl-β- d -galactopyranoside, NPG) is approximately constant for certain grou