نتایج جستجو برای: peptide analogues

تعداد نتایج: 185427  

2017
Mary-Patricia Yannakakis Carmen Simal Haralambos Tzoupis Maria Rodi Narges Dargahi Monica Prakash Athanasia Mouzaki James A. Platts Vasso Apostolopoulos Theodore V. Tselios

Encephalitogenic T cells are heavily implicated in the pathogenesis of multiple sclerosis (MS), an autoimmune demyelinating disease of the central nervous system. Their stimulation is triggered by the formation of a trimolecular complex between the human leukocyte antigen (HLA), an immunodominant myelin basic protein (MBP) epitope, and the T cell receptor (TCR). We detail herein our studies dir...

Journal: :FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2002
Andrea S Gobin Jennifer L West

We have developed synthetic hydrogel extracellular matrix (ECM) analogues that can be used to study mechanisms involved in cell migration, such as receptor-ligand interactions and proteolysis. The biomimetic hydrogels consist of bioinert polyethylene glycol diacrylate derivatives with proteolytically degradable peptide sequences included in the backbone of the polymer and adhesive peptide seque...

2017
Aleksandra Marciniak Justyna Brasuń

Peptide receptor radionuclide therapy (PRRT) is a promising way to treat patients with inoperable tumors or metastatic neuroendocrine tumors. This therapeutic strategy is using radiolabeled peptides, which are capable of selective biding to receptors overexpressed in the cancer cells. One of the group of receptor-avid peptide used in the PRRT are the analogues of somatostatin (SST) connected to...

2012
Ricardo A W Neves Filho Sebastian Stark Bernhard Westermann Ludger A Wessjohann

Two syntheses of natural viridic acid, an unusual triply N-methylated peptide with two anthranilate units, are presented. The first one is based on peptide-coupling strategies and affords the optically active natural product in 20% overall yield over six steps. A more economical approach with only four steps leads to the similarly active racemate by utilizing a Ugi four-component reaction (Ugi-...

Journal: :European journal of medicinal chemistry 2012
Pilar Ventosa-Andrés Angel M Valdivielso Ioannis Pappos M Teresa García-López Nikos E Tsopanoglou Rosario Herranz

By applying a diversity oriented synthesis strategy for the search of new antagonists of the thrombin receptor PAR1, a series of peptide-based ureas and thioureas, including analogues of the PAR1 reference antagonist RWJ-58259, has been designed and synthesized. The general synthetic scheme involves reduction of basic amino acid-derived amino nitriles by hydrogen transfer from hydrazine monohyd...

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