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Artykuły w czasopismach na temat "Cage-amine"
Long, Augustin, Olivier Perraud, Erwann Jeanneau, Christophe Aronica, Jean-Pierre Dutasta i Alexandre Martinez. "A hemicryptophane with a triple-stranded helical structure". Beilstein Journal of Organic Chemistry 14 (24.07.2018): 1885–89. http://dx.doi.org/10.3762/bjoc.14.162.
Pełny tekst źródłaKoutsantonis, George A., Gareth L. Nealon, Craig E. Buckley, Mark Paskevicius, Laurent Douce, Jack M. Harrowfield i Alasdair W. McDowall. "Wormlike Micelles from a Cage Amine Metallosurfactant". Langmuir 23, nr 24 (listopad 2007): 11986–90. http://dx.doi.org/10.1021/la701283b.
Pełny tekst źródłaMa, Michelle T., Margaret S. Cooper, Rowena L. Paul, Karen P. Shaw, John A. Karas, Denis Scanlon, Jonathan M. White, Philip J. Blower i Paul S. Donnelly. "Macrobicyclic Cage Amine Ligands for Copper Radiopharmaceuticals: A Single Bivalent Cage Amine Containing Two Lys3-bombesin Targeting Peptides". Inorganic Chemistry 50, nr 14 (18.07.2011): 6701–10. http://dx.doi.org/10.1021/ic200681s.
Pełny tekst źródłaModak, Ritwik, Bijnaneswar Mondal, Prodip Howlader i Partha Sarathi Mukherjee. "Self-assembly of a “cationic-cage” via the formation of Ag–carbene bonds followed by imine condensation". Chemical Communications 55, nr 47 (2019): 6711–14. http://dx.doi.org/10.1039/c9cc02341k.
Pełny tekst źródłaRivera, Augusto, Martı́n E. Núñez, Martha S. Morales-Rı́os i Pedro Joseph-Nathan. "Preparation of cage amine 1,3,6,8-tetraazatricyclo[4.3.1.13,8]undecane". Tetrahedron Letters 45, nr 41 (październik 2004): 7563–65. http://dx.doi.org/10.1016/j.tetlet.2004.08.123.
Pełny tekst źródłaHong, Dae Ho, Brian J. Knight, Vincent J. Catalano i Leslie J. Murray. "Isolation of chloride- and hydride-bridged tri-iron and -zinc clusters in a tris(β-oxo-δ-diimine) cyclophane ligand". Dalton Transactions 48, nr 26 (2019): 9570–75. http://dx.doi.org/10.1039/c9dt00799g.
Pełny tekst źródłaSmith, Paul H., Zelideth E. Reyes, Chi Woo Lee i Kenneth N. Raymond. "Characterization of a series of lanthanide amine cage complexes". Inorganic Chemistry 27, nr 23 (listopad 1988): 4154–65. http://dx.doi.org/10.1021/ic00296a015.
Pełny tekst źródłaKlein, Liv B., Thorbjørn J. Morsing, Ruth A. Livingstone, Dave Townsend i Theis I. Sølling. "The effects of symmetry and rigidity on non-adiabatic dynamics in tertiary amines: a time-resolved photoelectron velocity-map imaging study of the cage-amine ABCO". Physical Chemistry Chemical Physics 18, nr 14 (2016): 9715–23. http://dx.doi.org/10.1039/c5cp07910a.
Pełny tekst źródłaGeue, RJ, P. Osvath, AM Sargeson, KR Acharya, SB Noor, TNG Row i K. Venkatesan. "The Reaction of a Nitro-Capped Cobalt(III) Cage Complex With Base: the Crystal Structure of a Contracted Cage Complex, and the Mechanism of Its Formation". Australian Journal of Chemistry 47, nr 3 (1994): 511. http://dx.doi.org/10.1071/ch9940511.
Pełny tekst źródłaAcharyya, Koushik, i Partha Sarathi Mukherjee. "Shape and size directed self-selection in organic cage formation". Chemical Communications 51, nr 20 (2015): 4241–44. http://dx.doi.org/10.1039/c5cc00075k.
Pełny tekst źródłaRozprawy doktorskie na temat "Cage-amine"
Lengkeek, Nigel Andrew. "Functional cage-amine complexes : polymerisable metallomonomers and multi-cage complexes". University of Western Australia. School of Biomedical, Biomolecular and Chemical Sciences, 2008. http://theses.library.uwa.edu.au/adt-WU2008.0138.
Pełny tekst źródłaNealon, Gareth L. "Substituted cage amines : towards new functional metalloassemblies". University of Western Australia. School of Biomedical and Chemical Sciences, 2007. http://theses.library.uwa.edu.au/adt-WU2007.0215.
Pełny tekst źródłaMa, Michelle Therese. "Coordination of transition metals to peptides : (i) ruthenium and palladium metal clips that induce pentapeptides to be [alpha]-helical in water : (ii) synthesis of peptides incorporating a cage amine ligand for chelation of copper radioisotopes /". Connect to thesis, 2010. http://repository.unimelb.edu.au/10187/6715.
Pełny tekst źródłaMa, Michelle Therese. "Coordination of transition metals to peptides: (i) Ruthenium and palladium metal clips that induce pentapeptides to be α-helical in water; (ii) Synthesis of peptides incorporating a cage amine ligand for chelation of copper radioisotopes". 2010. http://repository.unimelb.edu.au/10187/6715.
Pełny tekst źródłaShort peptide sequences do not form thermodynamically stable α-helices in water. The capacity of two metal clips, cis-[Ru(NH3)4(solvent)2]2+ and cis [Pd(en)(solvent)2]2+ to induce α-helicity in peptides that are five amino acids long, Ac HARAH NH2 and Ac MARAM-NH2 has been explored. In all cases at pH < 5, the metal ions bind to the side-chains of amino acid residues at positions i, i+4 of the pentapeptides resulting in formation of bidentate macrocyclic species. Circular dichroism and 1H nuclear magnetic resonance data indicate that the metal complexes of Ac-MARAM-NH2 are highly α helical in water, and in the most spectacular case, coordination of Ac-MARAM-NH2 to cis-[Ru(NH3)4(solvent)2]2+ results in up to 80% α-helicity. In contrast, metal complexes of Ac-HARAH-NH2 exhibit significantly less α-helicity in water.
64Cu-radiolabelled peptides have been investigated for their ability to target specific tissue or cell types. These peptides require a chelating group that binds copper ions strongly. Macrobicyclic hexaamine ligands, based on the compound commonly referred to as “sarcophagine”, have demonstrated extremely high stability under biological conditions. Here we describe the synthesis of diaminosarcophagine chelators with carboxylate groups for conjugation to peptides. These new chelators have been attached to the N-terminus or lysine side-chain of biologically-active peptides, including Tyr3 octreotate, Lys3-bombesin and an integrin targeting peptide. Spectroscopic and voltammetric studies of these species suggest that the conjugated sarcophagine group retains the high metal binding affinity and structural properties of the parent species, diaminosarcophagine. These are among the first sarcophagine-peptide compounds that have been properly characterised. The new sarcophagine-peptide conjugates can be easily radiolabelled with 64Cu2+ over a wide pH range at ambient temperature.