Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Maja Roščić"'
Publikováno v:
Croatica Chemica Acta, Vol 88, Iss 3, Pp 281-287 (2015)
Both the chemistry and consequences of the nonenzymatic reaction between reducing sugars and reactive amino groups of amino acids, peptides and proteins (known as the Maillard reaction), have received considerable attention in food and health science
Externí odkaz:
https://doaj.org/article/61a94b2601634dfbbb519bb7de3bbad1
Publikováno v:
Croatica Chemica Acta, Vol 88, Iss 3, Pp 281-287 (2015)
Croatica Chemica Acta
Volume 88
Issue 3
Croatica Chemica Acta
Volume 88
Issue 3
Both the chemistry and consequences of the nonenzymatic reaction between reducing sugars and reactive amino groups of amino acids, peptides and proteins (known as the Maillard reaction), have received considerable attention in food and health science
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1d3a5b724e58977e18848dda2a5e84f
http://hrcak.srce.hr/file/221511
http://hrcak.srce.hr/file/221511
Publikováno v:
European Journal of Organic Chemistry. 2004:4641-4647
In this thesis a computational complement to experimental observables will be presented. Computational tools such as molecular dynamics and quantum chemical tools will be used to aid in the interpretation of experimentally (NMR) obtained structural d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba980ea4ab3a33c669d21b920551fa2a
https://doi.org/10.1002/ejoc.200400391
https://doi.org/10.1002/ejoc.200400391
Publikováno v:
Journal of Peptide Science. 10:47-55
Comparative studies based on x-ray crystallography and NMR spectroscopy were used for structural characterization of the novel minor, imidazolidinone moiety containing, product 2b of the Maillard reaction obtained in vitro by using the galactose-modi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7de1f80a3b1a2a6dd677fad54f2d5b5
https://doi.org/10.1002/psc.481
https://doi.org/10.1002/psc.481
Autor:
Lidija Barišić, Vladimir Rapić, Maja Roščić, Mojca Čakić Semenčić, Štefica Horvat, Monika Kovačević
Publikováno v:
Carbohydrate research. 346(5)
The two structurally interesting bioorganometallic analogues of muramyldipeptide (MDP) with potential immunomodulatory activity were synthesized starting from the O-protected N-acetylmuramic acid (MurNAc), L- or D-Ala and 1'-aminoferrocene-1-carboxyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f312c7d3bcf1d11e365ddfb7b7117a1
https://pubmed.ncbi.nlm.nih.gov/21316038
https://pubmed.ncbi.nlm.nih.gov/21316038
Autor:
Andrea Togninelli, Sonia Delle Fratte, Milan Mesic, Emiliano Castiglioni, Luigi Piero Stasi, Mario Smehil, Massimo Gianotti, Maurizio Botta, Michele Dal-Cin, Renzo Carletti, Francesca Pavone, Laura Piccoli, Mark Wigglesworth, Denana Korajac, Slavko Rast, Maja Roščić, Stephen J. Brough, Anna Sava, Corrado Corti, Giancarlo Merlo, Marija Lovrić
Publikováno v:
Journal of medicinal chemistry. 53(21)
Histamine H(1) and serotonin 5-HT(2A) receptors mediate two different mechanisms involved in sleep regulation: H(1) antagonists are sleep inducers, while 5-HT(2A) antagonists are sleep maintainers. Starting from 9'a, a novel spirotetracyclic compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f441b5897e4354fcfc1d72f68a14507c
https://pubmed.ncbi.nlm.nih.gov/20942472
https://pubmed.ncbi.nlm.nih.gov/20942472
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1fb0e763906f827c1c76f7ad96c72fd
https://doi.org/10.1002/chin.199847237
https://doi.org/10.1002/chin.199847237
Autor:
Maja Roščić, Štefica Horvat
The formation of glycosylation products in model systems consisting of d-glucuronic acid (GlcA) and lysine-containing peptides, such as Lys-Gly-Gly-Phe-Leu (1), Gly-Lys-Gly-Phe-Leu (4) and Ac-Gly-Lys-Gly-Phe-Leu (6), was examined to evaluate the site
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::760a05e33bc7b75e7ab50683d4301b9f
https://www.bib.irb.hr/437405
https://www.bib.irb.hr/437405
Autor:
Matija Gredičak, Milica Perc, Ivanka Jerić, Marijeta Kralj, Lidija Varga-Defterdarović, Andreja Jakas, Maja Roščić, Štefica Horvat, Lidija Šuman
Publikováno v:
Chemical biologydrug design. 73(2)
A series of new backbone-modified Leu- and Met-enkephalin analogues (13-20 a and b) were synthesized. Backbone manipulations involved the replacement of the Gly2 residue in Tyr-Gly-Gly-Phe-Leu/Met with side-chain glucosylated or adamantylated D/L-asp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb627f7a3078aa3e41e2d820cae229c7
https://pubmed.ncbi.nlm.nih.gov/19207428
https://pubmed.ncbi.nlm.nih.gov/19207428
Publikováno v:
Chemical biologydrug design. 70(1)
The kinetics of formation and identity of the reaction products of the glucuronic acid with three representative opioid peptides were investigated in vitro. Peptides were conjugated with glucuronic acid either in solution or under dry-heating conditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8363702036e7428f5309ef9d56fe52c7
https://pubmed.ncbi.nlm.nih.gov/17630992
https://pubmed.ncbi.nlm.nih.gov/17630992