Добірка наукової літератури з теми "Pseudopeptidic molecules"
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Статті в журналах з теми "Pseudopeptidic molecules"
Alfonso, Ignacio. "From simplicity to complex systems with bioinspired pseudopeptides." Chemical Communications 52, no. 2 (2016): 239–50. http://dx.doi.org/10.1039/c5cc07596c.
Повний текст джерелаBijesh, M. B., N. U. Dheepthi, Appa Rao Sapala, Ashutosh Shandilya, Kedar Khare, and V. Haridas. "Chiral and non-chiral assemblies from lipidated serine-based pseudopeptidic molecules." Molecular Systems Design & Engineering 1, no. 2 (2016): 163–68. http://dx.doi.org/10.1039/c6me00009f.
Повний текст джерелаOstankovitch, Marina, Gilles Guichard, Francine Connan, Sylviane Muller, Aude Chaboissier, Johan Hoebeke, Jeannine Choppin, Jean-Paul Briand, and Jean-Gérard Guillet. "A Partially Modified Retro-Inverso Pseudopeptide Modulates the Cytokine Profile of CTL Specific for an Influenza Virus Epitope." Journal of Immunology 161, no. 1 (July 1, 1998): 200–208. http://dx.doi.org/10.4049/jimmunol.161.1.200.
Повний текст джерелаFaggi, Enrico, Santiago V. Luis та Ignacio Alfonso. "Minimalistic amino amides as models to study N–H⋯π interactions and their implication in the side chain folding of pseudopeptidic molecules". RSC Advances 3, № 29 (2013): 11556. http://dx.doi.org/10.1039/c3ra41843j.
Повний текст джерелаMehrazma, Banafsheh, Anahit Petoyan, Stanley K. A. Opare та Arvi Rauk. "Interaction of the N-AcAβ(13–23)NH2 segment of the beta amyloid peptide with beta-sheet-blocking peptides: site and edge specificity". Canadian Journal of Chemistry 94, № 6 (червень 2016): 583–92. http://dx.doi.org/10.1139/cjc-2016-0033.
Повний текст джерелаEsteve, Ferran, Alexis Villanueva-Antolí, Belén Altava, Eduardo García-Verdugo, and Santiago V. Luis. "Unravelling the Supramolecular Driving Forces in the Formation of CO2-Responsive Pseudopeptidic Low-Molecular-Weight Hydrogelators." Gels 8, no. 6 (June 20, 2022): 390. http://dx.doi.org/10.3390/gels8060390.
Повний текст джерелаDharmashekar, Chandan, Bhargav Shreevatsa, Anisha S. Jain, Bhavana Harendra, Sushma Pradeep, Prashanth M. Vishwanath, Pranav Singh, et al. "Evaluating the Antimicrobial and Anti-Hemolytic Activity of Synthesized Pseudopeptide against Leptospiral Species: In Silico and In Vitro Approach." Molecules 28, no. 3 (January 22, 2023): 1106. http://dx.doi.org/10.3390/molecules28031106.
Повний текст джерелаCalbo, Sébastien, Gilles Guichard, Philippe Bousso, Sylviane Muller, Philippe Kourilsky, Jean-Paul Briand, and Jean-Pierre Abastado. "Role of Peptide Backbone in T Cell Recognition." Journal of Immunology 162, no. 8 (April 15, 1999): 4657–62. http://dx.doi.org/10.4049/jimmunol.162.8.4657.
Повний текст джерелаAmini, Zohreh, Mohammad Hossein Fatemi та Arvi Rauk. "Molecular dynamics studies of a β-sheet blocking peptide with the full-length amyloid beta peptide of Alzheimer’s disease". Canadian Journal of Chemistry 94, № 10 (жовтень 2016): 833–41. http://dx.doi.org/10.1139/cjc-2016-0267.
Повний текст джерелаMoure, Alejandra, Santiago V. Luis, and Ignacio Alfonso. "Efficient Synthesis of Pseudopeptidic Molecular Cages." Chemistry - A European Journal 18, no. 18 (March 29, 2012): 5496–500. http://dx.doi.org/10.1002/chem.201104045.
Повний текст джерелаДисертації з теми "Pseudopeptidic molecules"
B, Bijesh M. "Self-assembly and anion recognition properties of designer pseudopeptidic molecules." Thesis, IIT Delhi, 2017. http://localhost:8080/iit/handle/2074/7221.
Повний текст джерелаCalbo, Sébastien. "Role du squelette carbone du peptide antigenique dans l'interaction avec les molecules du complexe majeur d'histocompatibilite et dans la degenerescence de la reconnaissance t : immunologie." Paris 5, 1998. http://www.theses.fr/1998PA05N141.
Повний текст джерелаDeng, Cheng. "Analyses conformationnelles de nouveaux systèmes organisés biomimétiques." Thesis, Université de Lorraine, 2014. http://www.theses.fr/2014LORR0247/document.
Повний текст джерелаThe subject of this thesis deals with the structural studies of a new generation of oligomers, so called foldamers, constructed from pseudopeptidic mimics and able to adopt determined secondary structures. Three families of oligomers were investigated. For each oligomer several spectroscopic methods have been used combined with molecular modeling in order to characterize their structural properties. The first family was studied in collaration with the group of Muriel Amblard and Monique Calmès at IBMM in Montpellier. We have evaluated the structural properties of the motif (S)-ABOC. Several oligomers of varying sizes were synthesized and we have shown that the pattern (S)-ABOC, when introduced into a peptide sequence, is capable of generating beta turn. The sequence of these turn leads to the formation of helices, which, according to associated pseudo-peptide patterns shows different characteristics. The second project discussed the conformation of oligomers family formed from constrainted thiazole monomers. We have shown that this pattern developed by Ludovic Maillard at IBMM in Montpellier adopted pseudocycles C9 which led to helices. THis property was observed starting from the tetramer. The third family of oligomers comes from the LCPM, alternating oligomers of alpha amino acids and aza amino acids, in which the alpha carbon has been replaced by a nitrogen atom. We showed that the pattern aza induces folding of the beta turn, facilitating the cyclization of the molecule. In this thesis we have characterized the properties to self-structuring of three families of pseudopeptide foldamers by combining experimental results from nuclear magnetic resonance, infrared spectroscopy, circular dichroism and X-ray diffraction combined with molecular modeling calculations. Our study lists the properties of each pattern to form secondary structure elements and to induce the formation of foldamers
Legrand, Baptiste. "Analyse d'interactions moléculaires par RMN : Étude de la DHFR en présence d'osmolytes et structures de pseudopeptides antimicrobiens en environnement." Phd thesis, Rennes 1, 2009. https://tel.archives-ouvertes.fr/tel-00453405.
Повний текст джерелаThe osmolytes are small molecules accumulated by cells of a wide variety of organisms in response to hyperosmotic stress to maintain the cellular volume. Nervetheless, enzyme activity is inhibited by these cosolutes and the molecular basis of their effects on the proteins properties is of great interest. We studied the DHFR in presence of the osmolytes. We demonstrate that its overall structure is maintained. While the osmolytes stabilize the DHFR structure, they inhibit its activity at the same time. The k[index :]off, of substrate analogues decreases with increasing the osmolyte concentrations and reflects the variation of DHFR catalytic rate. The study of the DHFR dynamic on several timescales gives answer of the origins of the DHFR inhibition in presence of osmolytes. The second chapter concerns the study of the structure-activity relationship of antimicrobial peptides. The main objective of this project is to develop new drugs. We solved NMR solution structure of in various model membranes
Hegde, Raghurama P. "X-ray Crystallographic Studies Of Designed Peptides, Self Assembling Pseudopeptides And Molecular Modeling." Thesis, 2006. https://etd.iisc.ac.in/handle/2005/402.
Повний текст джерелаHegde, Raghurama P. "X-ray Crystallographic Studies Of Designed Peptides, Self Assembling Pseudopeptides And Molecular Modeling." Thesis, 2006. http://hdl.handle.net/2005/402.
Повний текст джерелаGorczyca, Marcelina. "Badanie oddziaływań związków biologicznie aktywnych z modelowymi membranami lipidowymi." Praca doktorska, 2015. https://ruj.uj.edu.pl/xmlui/handle/item/45209.
Повний текст джерелаЧастини книг з теми "Pseudopeptidic molecules"
Mucha, Artur, and Paweł Kafarski. "Peptide and Pseudopeptide Bond Synthesis in Phosphorus Dipeptide Analogs." In Methods in Molecular Biology, 287–301. New York, NY: Springer US, 2019. http://dx.doi.org/10.1007/978-1-0716-0227-0_20.
Повний текст джерелаVogel, David M., Sylvie Blondelle, and Arno F. Spatola. "Low Molecular Weight Ψ[CH2NH] Pseudopeptides Yield Potent Antimicrobial Agents." In Peptides: The Wave of the Future, 762–63. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_356.
Повний текст джерелаSawyer, Tomi K., Jackson B. Hester, Heinrich J. Schostarez, S. Thaisrivongs, Gordon L. Bundy, Li Liu, V. Susan Bradford, et al. "Exploiting the Molecular Template of Angiotensinogen in the Discovery and Design of Peptidyl, Pseudopeptidyl and Peptidemimetic Inhibitors of Human Renin: A Structure-Activity Perspective." In Advances in Experimental Medicine and Biology, 307–23. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4684-6012-4_37.
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