Calixarene-based multivalent ligands

被引:360
作者
Baldini, L.
Casnati, A.
Sansone, F.
Ungaro, R.
机构
[1] Univ Parma, Dipartimento Chim Organ & Ind, I-43100 Parma, Italy
[2] Consorzio INSTM, I-50121 Florence, Italy
关键词
D O I
10.1039/b603082n
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multivalency is a powerful concept which explains the strong binding observed in biological systems and guides the design and synthesis of ligands for self-assembly and molecular recognition in Chemistry. The phenol-formaldehyde cyclic oligomers, called calixarenes, have been used as scaffolds for the synthesis of multivalent ligands thanks to the fact that they have a variable number of reactive positions for attaching the ligating functions, well defined conformational properties and, in some cases, cavities of molecular dimensions eventually able to encapsulate guest species. This tutorial review illustrates the fundamental aspects of multivalency and the properties of calixarene-based multivalent ligands in lectin binding and inhibition, DNA condensation and cell transfection, protein surface recognition, self-assembly, crystal engineering, and nanofabrication.
引用
收藏
页码:254 / 266
页数:13
相关论文
共 42 条
[1]   Macrocyclic glycoclusters: From amphiphiles through nanoparticles to glycoviruses [J].
Aoyama, Y .
CHEMISTRY-A EUROPEAN JOURNAL, 2004, 10 (03) :588-593
[2]   A synthetic divalent cholera toxin glycocalix[4]arene ligand having higher affinity than natural GM1 oligosaccharide [J].
Arosio, D ;
Fontanella, M ;
Baldini, L ;
Mauri, L ;
Bernardi, A ;
Casnati, A ;
Sansone, F ;
Ungaro, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (11) :3660-3661
[3]   Writing patterns of molecules on molecular printboards [J].
Auletta, T ;
Dordi, B ;
Mulder, A ;
Sartori, A ;
Onclin, S ;
Bruinink, CM ;
Péter, M ;
Nijhuis, CA ;
Beijleveld, H ;
Schönherr, H ;
Vancso, GJ ;
Casnati, A ;
Ungaro, R ;
Ravoo, BJ ;
Huskens, J ;
Reinhoudt, DN .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (03) :369-373
[4]   Designing nanoporous crystalline materials by self-assembly:: 2D hydrogen-bonded networks from upper rim calix[4]arene diamide derivatives [J].
Baldini, Laura ;
Sansone, Francesco ;
Massera, Chiara ;
Casnati, Alessandro ;
Ugozzoli, Franco ;
Ungaro, Rocco .
INORGANICA CHIMICA ACTA, 2007, 360 (03) :970-980
[5]   Mimicking gangliosides by design: Mimics of GM1 headgroup [J].
Bernardi, A ;
Arosio, D ;
Sonnino, S .
NEUROCHEMICAL RESEARCH, 2002, 27 (7-8) :539-545
[6]   Topologically novel multiple rotaxanes and catenanes based on tetraurea calix[4]arenes [J].
Bogdan, Anca ;
Rudzevich, Yuliya ;
Vysotsky, Myroslav O. ;
Boehmer, Volker .
CHEMICAL COMMUNICATIONS, 2006, (28) :2941-2952
[7]   Peptido- and glycocalixarenes: Playing with hydrogen bonds around hydrophobic cavities [J].
Casnati, A ;
Sansone, F ;
Ungaro, R .
ACCOUNTS OF CHEMICAL RESEARCH, 2003, 36 (04) :246-254
[8]  
Casnati A, 2001, CALIXARENES 2001, P365
[9]  
Choi S.K., 2004, SYNTHETIC MULTIVALEN
[10]   Synthesis and lectin binding ability of glycosamino acid-calixarenes exposing GlcNAc clusters [J].
Consoli, GML ;
Cunsolo, F ;
Geraci, C ;
Sgarlata, V .
ORGANIC LETTERS, 2004, 6 (23) :4163-4166