A simple method for the synthesis of pH-responding polymers containing barbituric acid moieties is described.
The synthesis of various block copolymers containing phosphonic acid moieties is described.
SAR on the substituting groups, as well as on modification of P1 and P4 moieties is described.
The synthesis of new polyamine derivatives containing dimeric quinoline (3a c), cinnoline (4a c) and phthalimide (7a c and 8a c) moieties is described.
Their structures are versatile and many different hydrophilic and hydrophobic moieties are described in literature (Hausmann and Syldatk 2014; Kügler et al. 2015).
The photo-isomerization of the azobenzene moieties is described by implementing a photo-switching potential that represents the light-excited energy transition path.
The design, synthesis, biological activity, and the binding modes of non-covalent thrombin inhibitors featuring P1-4,5,6,7-tetrahydroindazole, 5,6,7,8-tetrahydroquinazoline, and 4,5,6,7-tetrahydrobenzothiazole 4,5,6,7-tetrahydrobenzothiazole
The synthesis and in vitro characterization of novel RXR-selective ligands possessing various substituted 1-benzofuran or 1-benzothiophene moieties are described.
The cytokine field is constantly growing as novel moieties are described.
In a second step of the interaction, however, intercalation of the C-terminal proximal hydrophobic peptide part into the lipid A hydrophobic moiety was described [ 34].
