Global ETD Search
Search theses and dissertations gathered from participating repositories worldwide. Every result links back to the library that holds it. No account is needed.
Results
Showing 1 to 8 of 8 for “"Peptides--Synthesis"”.
-
AGEing Peptides: Synthesis and Analysis of Peptides Site-Specifically Modified by Advanced Glycation Endproducts
… biochemistry by providing access to synthetic peptides that can be site-specifically modified by particular AGEs. Five prominent lysyl AGEs, Nε-carboxymethyllysine (CML), Nε-carboxyethyllysine (CEL), pyrraline, glyoxal lysine dimer (GOLD), and methylglyoxal lysine dimer (MOLD), were selected as …
-
SYNTHESIS, BIOLOGICAL ACTIVITY AND CONFORMATIONAL ANALYSIS OF FRAGMENT ANALOGUES OF ALPHA-MELANOTROPIN (PEPTIDE, STRUCTURE-FUNCTION, PHENYLGLYCINE, NMR, TETRAHYDROISOQUINOLINE-3-CARBOXYLATE).
α-MSH (α-melanotropin) is a naturally occurring linear tridecapeptide (Ac-Ser-Tyr-Ser-Met-Glu-His-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH₂) that is primarily known for its ability to stimulate integumental melanocytes and more recently has been implicated in a variety of physiological and neurological …
-
A computational study of Trishomocubane amino acid dipeptide
A dissertation submitted in partial fulfilment of the requirements for the degree of Master of Technology: Chemistry, Durban Institute of Technology, Durban, South Africa, 2004.
-
ΜΕΛΕΤΗ ΤΗΣ ΔΙΑΜΟΡΦΩΣΗΣ ΚΑΙ ΤΗΣ ΜΟΡΙΑΚΗΣ ΔΥΝΑΜΙΚΗΣ ΤΩΝ ΕΓΚΕΦΑΛΙΝΩΝ ΜΕ ΦΑΣΜΑΤΟΣΚΟΠΙΑ ΠΥΡΗΝΙΚΟΥ ΜΑΓΝΗΤΙΚΟΥ ΣΥΝΤΟΝΙΣΜΟΥ (17Ο-NMR) ΚΑΙ ΥΠΕΡΥΘΡΟΥ...
… SIDE- CHAIN CONFORMATION OF TYROSINE CONTAINING PEPTIDES, SEVERAL 17O SELECTIVELY ENRICHED MODEL COMPOUNDS WERE PREPARED. 17O-NMR SPECTROSCOPY WAS PROVED TO BE A VALUABLE TOOL FOR THE INVESTIGATION OF THE IONIZATION STATE OF THE PHENOL GROUP. IR-FT STUDIES REVEALED THAT THE IN PLANE C-O-H BENDING …
-
Design, Synthesis, and Evaluation of Covalent CADA Analogues as Potent TLR4 Downmodulator for the Treatment of Opioid Use Disorder
… of TLR4 to address OUD. This study explores the synthesis of different covalent CADA analogues targeting the SP of TLR4, which contains a cysteine residue in its hydrophobic region, making it a viable target for covalent modulation. So far, more than twenty covalent CADA analogues have been …