نتایج جستجو برای: macrocyclic ligands

تعداد نتایج: 107929  

Journal: :iranian journal of chemistry and chemical engineering (ijcce) 1999
aziz shahrisa reza tabrizi

new macrocyclic polyether-diester ligands (3-5) containing the 4h-pyran-4-one subcyclic unit have been prepared by treating various glycols with dimethyl chelidonate (10). in the reaction of compound 10 with ethylene glycol and diethylene glycol, two noncyclic diester and tetraester (6-9) were produced in each case. the new marcocyclic ligand 4 formed stable complexes with benzylammonium perchl...

Aziz Shahrisa Reza Tabrizi

New macrocyclic polyether-diester ligands (3-5) containing the 4H-pyran-4-one subcyclic unit have been prepared by treating various glycols with dimethyl chelidonate (10). In the reaction of compound 10 with ethylene glycol and diethylene glycol, two noncyclic diester and tetraester (6-9) were produced in each case. The new marcocyclic ligand 4 formed stable complexes with benzylammonium pe...

2011
DEVENDRA KUMAR

A series of 18-membered macrocyclic complexes of metal Ni(II) of the type [M(H2Cy )] have been synthesized and characterized on the basis of spectral, magnetic and conductivity studies. The macrocyclic ligands H 4 Cy1-4 (Fig. 1) are tetrabasic having four imido hydrogen but behave in a dibasic manner. Out of eight nitrogens, four imido and four imino, ligands utilize four imido nitrogens for sq...

Journal: :Dalton transactions 2012
Diana C F Monteiro Roger M Phillips Benjamin D Crossley Jake Fielden Charlotte E Willans

A diverse library of cationic silver complexes bearing bis(N-heterocyclic carbene) ligands have been prepared which exhibit cytotoxicity comparable to cisplatin against the adenocarcinomas MCF7 and DLD1. Bidentate ligands show enhanced cytotoxicity over monodentate and macrocyclic ligands.

Journal: :Dalton transactions 2013
Wei-Jie Gong Ying-Ying Liu Jin Yang Hua Wu Jian-Fang Ma Teng-Feng Xie

An unprecedented octahedral {Cd(30)} nanocage supported by twelve pendant-armed tetraacetate macrocyclic ligands was synthesized through the reaction of macrocyclic tetraethyl ester and Cd(OAc)(2)·2H(2)O in a 1 : 2 stoichiometry, where the surface photovoltage and photoluminescent properties have been studied for the nanocage.

2016
MONIKA KAMBOJ

The metal ion chemistry of macrocyclic ligands has now become a major subdivision of inorganic chemistry and is a growing area of research in inorganic and bioinorganic chemistry. The field of macrocylic chemistry of metals is developing very fast because of its applications and importance in the area of coordination chemistry. Macrocyclic ligands and their transition metal complexes have recei...

2009
Kanne Shanker Rondla Rohini P. Muralidhar Reddy Vadde Ravinder

A new family of Tetraazamacrocyclic Ru(II) complexes [RuCl2(L)] (where L = N4 donor macrocyclic ligands) have been synthesized by the reactions of [RuCl2(DMSO)4] with some of macrocyclic Schiff base ligands containing N4 donor groups. The complexes were characterized by elemental analysis, IR, H, C NMR, mass, electronic, molar conductance and magnetic susceptibility measurements. An octahedral ...

2015
Yu Gao Thomas Kodadek

There has been much discussion of the potential desirability of macrocyclic molecules for the development of tool compounds and drug leads. But there is little experimental data comparing otherwise equivalent macrocyclic and linear compound libraries as a source of protein ligands. In this Letter, we probe this point in the context of peptoid libraries. Bead-displayed libraries of macrocyclic a...

2016
Daniël Leenheer Peter ten Dijke Christopher John Hipolito

Monoclonal antibodies can bind with high affinity and high selectivity to their targets. As a tool in therapeutics or diagnostics, however, their large size (∼150 kDa) reduces penetration into tissue and prevents passive cellular uptake. To overcome these and other problems, minimized protein scaffolds have been chosen or engineered, with care taken to not compromise binding affinity or specifi...

Journal: :Molecules 2013
Christopher J Hipolito Yoshiki Tanaka Takayuki Katoh Osamu Nureki Hiroaki Suga

The random non-standard peptide integrated discovery (RaPID) system has proven to be a powerful approach to discover de novo natural product-like macrocyclic peptides that inhibit protein functions. We have recently reported three macrocyclic peptides that bind to Pyrococcus furiosus multidrug and toxic compound extrusion (PfMATE) transporter and inhibit the transport function. Moreover, these ...

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