Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Marek Lisowski"'
Publikováno v:
Tetrahedron Letters. 60:1814-1818
Solid phase-supported synthesis is a widely used strategy in peptide chemistry. A factor which limits the product purity is the individual stages yields. Here, we reported that the use of ultrasonic agitation allows to reduce tenfold the time of synt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fd52c62677c35023425f4728c480e5e
https://doi.org/10.1016/j.tetlet.2019.05.069
https://doi.org/10.1016/j.tetlet.2019.05.069
Autor:
Bartosz Setner, Zbigniew Szewczuk, Lucjan B. Jerzykiewicz, Marek Lisowski, Magdalena Wierzbicka
Publikováno v:
Organic & Biomolecular Chemistry. 16:825-831
Recently, we developed a novel non-fragmenting quaternary ammonium ionization tag for the mass spectrometric sensitive sequencing of peptides, based on the N-spiro proline residue (5-azoniaspiro[4.4.]nonyl-carbonyl). Herein, we present an unexpected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fe0cee992b0613f50bfa50a9096fac0
https://doi.org/10.1039/c7ob02926h
https://doi.org/10.1039/c7ob02926h
Autor:
Anna Adamska-Bartłomiejczyk, Alicja Kluczyk, Justyna Piekielna-Ciesielska, Anna Janecka, Szabolcs Dvorácskó, Grzegorz Wołczański, Marek Lisowski, Attila Borics, Csaba Tömböly
Publikováno v:
Journal of Peptide Science. 23:864-870
Three novel morphiceptin analogs, in which Pro in position 2 and/or 4 was replaced by cis-4-aminoproline connected with the preceding amino acid through the primary amino group, were synthesized. The opioid receptor affinities, functional assay resul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::789b6d1c32442be12456ce8b3b5bdfda
https://doi.org/10.1002/psc.3050
https://doi.org/10.1002/psc.3050
Autor:
Andrzej Marcinek, Joanna Katarzynska, Jolanta Artym, Iwona Kochanowska, Marek Lisowski, Michał Zimecki, Łukasz Piotrowski, Janusz Zabrocki, Stefan Jankowski, Robert Wieczorek, Karol Jędrzejczak
Publikováno v:
Peptides. 132:170365
The synthesis of new analogues of cyclolinopeptide A (CLA) and their linear precursors modified with (R)- and (S)-4-methylpseudoproline in the Pro3-Pro4 fragment are presented. The peptides were tested in comparison with cyclosporine A (CsA) in conca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9f8c280ef8fccb1f422349e587b5ab8
https://doi.org/10.1016/j.peptides.2020.170365
https://doi.org/10.1016/j.peptides.2020.170365
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 24(49)
A new method of synthesis of peptide conjugates with aromatic moieties substituted with two sulfhydryl groups at 1,3-positions is proposed. Amphiphilic peptides derivatized in such a way under oxidative conditions spontaneously form cyclic, covalent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::776d3790703ec373faddd352b80632bd
https://pubmed.ncbi.nlm.nih.gov/29901819
https://pubmed.ncbi.nlm.nih.gov/29901819
Autor:
Marek Lisowski, Grzegorz Wołczański
Publikováno v:
Journal of peptide science : an official publication of the European Peptide Society. 24(8-9)
N-(tert-butyloxycarbonyl) or N-(9-fluorenylmethoxycarbonyl) dipeptides with C-terminal (Z)-α,β-didehydrophenylalanine (∆Z Phe), (Z)-α,β-didehydrotyrosine (∆Z Tyr), (Z)-α,β-didehydrotryptophan (∆Z Trp), (Z)-α,β-didehydromethionine (∆Z
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2383d1a415f65da8152899d1f2d3ba85
https://pubmed.ncbi.nlm.nih.gov/29862598
https://pubmed.ncbi.nlm.nih.gov/29862598
Autor:
Anna, Adamska-Bartłomiejczyk, Attila, Borics, Csaba, Tömböly, Szabolcs, Dvorácskó, Marek, Lisowski, Alicja, Kluczyk, Grzegorz, Wołczański, Justyna, Piekielna-Ciesielska, Anna, Janecka
Publikováno v:
Journal of peptide science : an official publication of the European Peptide Society. 23(12)
Three novel morphiceptin analogs, in which Pro in position 2 and/or 4 was replaced by cis-4-aminoproline connected with the preceding amino acid through the primary amino group, were synthesized. The opioid receptor affinities, functional assay resul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1ae6248d4b0bc2125d1f95d0b14e979b
https://pubmed.ncbi.nlm.nih.gov/29110363
https://pubmed.ncbi.nlm.nih.gov/29110363
Publikováno v:
Peptides. 44:149-157
Neb -colloostatin (SIVPLGLPVPIGPIVVGPR), an insect oostatic factor found in the ovaries of the flesh fly Neobellieria bullata , strongly induces apoptosis in insect haemocytes. To explain the role of Ser 1 and Pro 4 residues of Neb -colloostatin in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea7fb2eef92a017c14cc2b90ccd35bec
https://doi.org/10.1016/j.peptides.2013.04.002
https://doi.org/10.1016/j.peptides.2013.04.002
Two phosphonodehydrotripeptides: Boc0–Gly1–Δ(Z)Phe2–α‐Abu3PO3Me2 and Boc0–Gly1–Δ(Z)Phe2–α‐Nva3PO3Et2
Publikováno v:
Acta Crystallographica Section C-Crystal Structure Communications. 69(3):277-281
The present paper reports the crystal structures of two short phosphonotripeptides (one in two crystal forms) containing one ΔPhe (dehydrophenylalanine) residue, namely dimethyl (3-{[tert-butoxycarbonylglycyl-α,β-(Z)-dehydrophenylalanyl]amino}prop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::188694f5caec3bfae66ffe985233f245
https://doi.org/10.1107/S0108270113002539
https://doi.org/10.1107/S0108270113002539
Publikováno v:
Amino Acids
Amino acids 45(4), 865-875 (2013). doi:10.1007/s00726-013-1534-9
Amino acids 45(4), 865-875 (2013). doi:10.1007/s00726-013-1534-9
Conformations of three pairs of dehydropeptides with the opposite configuration of the Delta Phe residue, Boc-Gly-Delta(Z/E)Phe-Phe-p-NA (Z- p -NA and E- p -NA), Boc-Gly-Delta(Z/E)Phe-Phe-OMe (Z-OMe and E-OMe), and Boc-Gly-Delta(Z/E)Phe-Phe-OH (Z-OH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0af27942de449de81df8a0605aa93e46
https://doi.org/10.1007/s00726-013-1534-9
https://doi.org/10.1007/s00726-013-1534-9