Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Luděk Lepša"'
Autor:
Šárka Klimešová, Luděk Lepša, Heda Černohorská, Alena Milcova, Jan Topinka, Jana Schmuczerova, Pavel Jinoch, Juraj Labaj
Publikováno v:
Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 742:2-10
Polycyclic aromatic hydrocarbons (PAH) are recognized as common environmental pollutants released into the environment from many natural as well as man-made sources, and some have been classified as potent carcinogens. The main representative of the
Publikováno v:
ELECTROPHORESIS. 23:2449-2456
A new analytical method for enantioselective separation of DL-amino acids derivatized by N-fluorenylmethoxycarbonyl-L-alanyl N-carboxyanhydride (FMOC-L-Ala-NCA) using capillary electrophoresis was developed. Separation parameters, such as composition
Publikováno v:
Peptides. 23:585-587
A new member of the AKH/RPCH family was isolated from the corpora cardiaca of the firebug Pyrrhocoris apterus. It is the second adipokinetic peptide identified in this species. The peptide was characterized and its structure was deduced from the mult
Autor:
Marie Přibylová, Veronika Šolínová, Jana Barthová, Tomáš Vaněk, Luděk Lepša, Tomislav Barth, Václav Kašička
Publikováno v:
Collection Symposium Series.
Publikováno v:
Collection Symposium Series.
Publikováno v:
Peptides: The Wave of the Future ISBN: 9789401039055
High or good yield is essential for peptide production. The side chain protecting groups are cleaved usually in solution, after peptide detachment from the solid carrier. This can, however, be accompanied by the loss of material and the decrease in y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0840ce8721a45ad814c4e5c39973987c
https://doi.org/10.1007/978-94-010-0464-0_37
https://doi.org/10.1007/978-94-010-0464-0_37
Publikováno v:
Collection of Czechoslovak Chemical Communications. 46:2734-2741
The reduction of terminal double bonds in the side chains on the rings A and E of pentacyclic triterpenoids by means of tris(triphenylphosphine)rhodium chloride permits selective reduction of dienes and labelling with deuterium with a low scattering.