Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Barbora Brazdova"'
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
Autor:
Vyacheslav V. Samoshin, Dmitriy E. Gremyachinskiy, Vyacheslav A. Chertkov, Barbora Brazdova, Elena K. Dobretsova, Alla K. Shestakova, Lidia P. Vatlina, Hans-Jörg Schneider
Publikováno v:
ARKIVOC, Vol 2005, Iss 4, Pp 129-141 (2005)
Externí odkaz:
https://doaj.org/article/4e85dbc7a459439dbb39993806e06360
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
Autor:
Yuen-Shan Wong, Barbora Brazdova, Xin Guo, Andrey V. Samoshin, Ningrong Zhang, Vyacheslav V. Samoshin, Sombo Koo, Andreas H. Franz
Publikováno v:
ARKIVOC, Vol 2005, Iss 4, Pp 129-141 (2005)
Cyclohexane-based conformationally controlled ionophores, the emerging new class of molecular switches, provide a new and promising approach to allosteric systems with negative cooperativity. Protonation of trans-2-aminocyclohexanols leads to dramati
Novel easily accessible glucosidase inhibitors: 4-hydroxy-5-alkoxy-1,2-cyclohexanedicarboxylic acids
Publikováno v:
Carbohydrate research. 344(3)
Glycosidases are very important enzymes involved in a variety of biochemical processes with a special importance to biotechnology, food industry, and pharmacology. Novel structurally simple inhibitors derived from cyclohexane-1,2-dicarboxylic acids w
Publikováno v:
Chemical Communications. :4774
Protonation-induced conformational change of lipid tails is reported as a novel strategy to render pH-sensitive lipid amphiphiles and lipid colloids.
Publikováno v:
Chemical Communications; Oct2008, Vol. 2008 Issue 39, p4774-4776, 3p