Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Katja Zebisch"'
Autor:
Valerie Voigt, Sabine Gebauer, Katja Zebisch, Iris Thondorf, Matthias Brandsch, Linda Laug, Sarah Schäfer
Publikováno v:
Bioorganic & Medicinal Chemistry. 19:6409-6418
The proton-coupled amino acid transporter hPAT1 has recently gained much interest due to its ability to transport small drugs thereby allowing their oral administration. A three-dimensional quantitative structure-activity relationship (3D QSAR) study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f507dcfa8dc518436333f990ea9a5255
https://doi.org/10.1016/j.bmc.2011.08.058
https://doi.org/10.1016/j.bmc.2011.08.058
Publikováno v:
The Journal of pharmacy and pharmacology. 65(4)
Objectives The pyridine alkaloid arecaidine is an ingredient of areca nut preparations. It is responsible for many physiological effects observed during areca nut chewing. However, the mechanism underlying its oral bioavailability has not yet been st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e717550babc166ed60f40bce41df6411
https://pubmed.ncbi.nlm.nih.gov/23488788
https://pubmed.ncbi.nlm.nih.gov/23488788
Autor:
Katja Zebisch, Matthias Brandsch
Publikováno v:
Amino acids. 44(2)
Mechanism and substrate specificity of the proton-coupled amino acid transporter 2 (PAT2, SLC36A2) have been studied so far only in heterologous expression systems such as HeLa cells and Xenopus laevis oocytes. In this study, we describe the identifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e662f34f0e00ad31a7ed044ed1b641b3
https://pubmed.ncbi.nlm.nih.gov/22711289
https://pubmed.ncbi.nlm.nih.gov/22711289
Autor:
Hannelore Daniel, Martin G. Hahn, Matthias Brandsch, Katja Zebisch, Reinhard H.H. Neubert, Claudia Wollesky, Gabor Kottra, Ilka Knütter, Wiebke Fischer
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 327(2)
Angiotensin-converting enzyme (ACE) inhibitors are often regarded as substrates for the H+/peptide transporters (PEPT)1 and PEPT2. Even though the conclusions drawn from published data are quite inconsistent, in most review articles PEPT1 is claimed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b074f24ab7ed61d298be02e66f958ceb
https://pubmed.ncbi.nlm.nih.gov/18713951
https://pubmed.ncbi.nlm.nih.gov/18713951
Autor:
Vadivel Ganapathy, Kristin Natho, Matthias Brandsch, Madlen Dorn, Katja Zebisch, Linda Metzner, Eva Bosse-Doenecke
Publikováno v:
Biochimica et biophysica acta. 1778(4)
The proton-coupled amino acid transporter 1 (PAT1) represents a major route by which small neutral amino acids are absorbed after intestinal protein digestion. The system also serves as a novel route for oral drug delivery. Having shown that H+ affec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a041d3b13478af3c6631b303008e3ac
https://pubmed.ncbi.nlm.nih.gov/18230330
https://pubmed.ncbi.nlm.nih.gov/18230330
Autor:
Sabine Gebauer, Klaus Neubert, Hannelore Daniel, Ilka Knütter, Matthias Brandsch, Iris Thondorf, Bianka Hartrodt, Gabor Kottra, P. Luckner, Annegret Biegel, M. Rastetter, Katja Zebisch, Stephan Theis
Publikováno v:
Amino acids. 31(2)
The H(+)/peptide cotransporter PEPT2 is expressed in a variety of organs including kidney, lung, brain, mammary gland, and eye. PEPT2 substrates are di- and tripeptides as well as peptidomimetics, such as beta-lactam antibiotics. Due to the presence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7208fa6e587377a5e263a7dcd099d7c
https://pubmed.ncbi.nlm.nih.gov/16868651
https://pubmed.ncbi.nlm.nih.gov/16868651
Publikováno v:
GBM Annual Fall meeting Berlin/Potsdam 2005. 2005
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4f599ba3944435ed647d402267d94ba
https://doi.org/10.1240/sav_gbm_2005_h_001283
https://doi.org/10.1240/sav_gbm_2005_h_001283