Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Grzegorz Wołczański"'
Peptide Stapling with Boronate Esters‐ A Reversible Folding of (Artificial) Peptide Chain to α‐Helix
Autor:
Monika Kijewska, Grzegorz Wołczański, Marta Światowska, Katarzyna Kędziora, Miłosz Pawlicki, Piotr Stefanowicz
Publikováno v:
Chemistry – A European Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c86792f4f760ec9d73d8957275f0053
https://doi.org/10.1002/chem.202301370
https://doi.org/10.1002/chem.202301370
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:
Piotr Stefanowicz, Abdul-Hamid M. Emwas, Angelika Czerwińska, Grzegorz Wołczański, Mateusz Waliczek, Monika Kijewska, Mariusz Jaremko, Samah Al-Harthi, Łukasz Jaremko, Zbigniew Szewczuk
Publikováno v:
Chemical communications (Cambridge, England). 56(62)
Amadori products (deoxyfructosyllysine derivatives) that can selectively interact with phenylboronic acids and borate ions were synthesized. The intramolecular interactions between the fructosyl moiety and phenylboronic acid incorporated into various
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2312b519ff9dcd6fa0290b39f7c1dc5b
https://pubmed.ncbi.nlm.nih.gov/32627786
https://pubmed.ncbi.nlm.nih.gov/32627786
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
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