Water-Soluble (Poly)acylhydrazones: Syntheses and Applications

被引:11
作者
Caillaud, Kilian [1 ]
Ladaviere, Catherine [1 ]
机构
[1] Univ Lyon, Univ Claude Bernard Lyon1, CNRS, Ingn Mat Polymeres,INSA Lyon,Univ Jean Monnet,UMR, F-69622 Lyon, France
关键词
acylhydrazone; dynamers; dynamic combinatorial chemistry; polyacylhydrazone; water-soluble polymers; DYNAMIC COVALENT POLYMERS; HYDRAZONE FORMATION; COMBINATORIAL CHEMISTRY; ANTIMICROBIAL ACTIVITY; ACYLHYDRAZONE DERIVATIVES; MOLECULAR AMPLIFICATION; NUCLEOPHILIC CATALYSIS; DNA COMPLEXATION; N-ACYLHYDRAZONE; LIBRARIES;
D O I
10.1002/macp.202200064
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Acylhydrazone-based (macro)molecules display an increasingly broad spectrum of applications, from small therapeutic molecules and metal-ions probes to self-healing films and biorelevant dynamic polymers. The acylhydrazone function is indeed of prime interest since its unique design combines hydrogen bonds, pH-dependent reversibility, ability to undergo molecular exchanges, and a possible polyvalency. However, a key parameter of its use in aqueous media is the associated water-solubility of the resulting (macro)molecule. This property can indeed become a limitation for applications requiring high concentrations or no organic cosolvent. This review first focuses on describing the acylhydrazone function, its properties, and its relevancy in dynamic combinatorial chemistry. Then it details the synthesis strategies (molecular design, cosolvent, reaction conditions) reported in the literature to ensure a sufficient solubilization of both single-bond and multiple-bond acylhydrazone (macro)molecules, together with their various applications.
引用
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页数:20
相关论文
共 142 条
[1]   Iminoboronate-Based Peptide Cyclization That Responds to pH, Oxidation, and Small Molecule Modulators [J].
Bandyopadhyay, Anupam ;
Gao, Jianmin .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2016, 138 (07) :2098-2101
[2]   Targeting bacteria via iminoboronate chemistry of amine-presenting lipids [J].
Bandyopadhyay, Anupam ;
McCarthy, Kelly A. ;
Kelly, Michael A. ;
Gao, Jianmin .
NATURE COMMUNICATIONS, 2015, 6
[3]  
Bartolami E., 2015, ANGEW CHEM, V127, P10321
[4]   Multivalent DNA recognition by self-assembled clusters: deciphering structural effects by fragments screening and evaluation as siRNA vectors [J].
Bartolami, Eline ;
Bessin, Yannick ;
Bettache, Nadir ;
Gary-Bobo, Magali ;
Garcia, Marcel ;
Dumy, Pascal ;
Ulrich, Sebastien .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2015, 13 (36) :9427-9438
[5]   From static to dynamic: escaping kinetic traps in hydrazone-based dynamic combinatorial libraries [J].
Beeren, Sophie R. ;
Pittelkow, Michael ;
Sanders, Jeremy K. M. .
CHEMICAL COMMUNICATIONS, 2011, 47 (26) :7359-7361
[6]  
Bhat VT, 2010, NAT CHEM, V2, P490, DOI [10.1038/nchem.658, 10.1038/NCHEM.658]
[7]   Acid-degradable polymers for drug delivery: a decade of innovation [J].
Binauld, Sandra ;
Stenzel, Martina H. .
CHEMICAL COMMUNICATIONS, 2013, 49 (21) :2082-2102
[8]   4-Aminophenylalanine as a Biocompatible Nucleophilic Catalyst for Hydrazone Ligations at Low Temperature and Neutral pH [J].
Blanden, Adam R. ;
Mukherjee, Kamalika ;
Dilek, Ozlem ;
Loew, Maura ;
Bane, Susan L. .
BIOCONJUGATE CHEMISTRY, 2011, 22 (10) :1954-1961
[9]   Synthesis and Study of Antimicrobial Activity of Water-Soluble Ammonium Acylhydrazones Based on New 1,ω-Alkylenebis(isatins) [J].
Bogdanov, A. V. ;
Zaripova, I. F. ;
Mustafina, L. K. ;
Voloshina, A. D. ;
Sapunova, A. S. ;
Kulik, N. V. ;
Mironov, V. F. .
RUSSIAN JOURNAL OF GENERAL CHEMISTRY, 2019, 89 (07) :1368-1376
[10]   Synthesis and antimicrobial activity evaluation of some novel water-soluble isatin-3-acylhydrazones [J].
Bogdanov, Andrei V. ;
Zaripova, Ilyuza F. ;
Voloshina, Alexandra D. ;
Strobykina, Anastasia S. ;
Kulik, Natalia V. ;
Bukharov, Sergey V. ;
Voronina, Julia K. ;
Khamatgalimov, Ayrat R. ;
Mironov, Vladimir F. .
MONATSHEFTE FUR CHEMIE, 2018, 149 (01) :111-117