Peptide‐Mimicking Poly(2‐oxazoline)s Displaying Potent Antimicrobial Properties
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Runhui Liu | Jiayang Xie | Min Zhou | Ximian Xiao | Zihao Cong | Weinan Jiang | Jingcheng Zou | Zhemin Ji | Jiayang Xie | Wenjing Zhang | J. Gu | Jiawei Gu
[1] Runhui Liu,et al. Breaking or following the membrane-targeting mechanism: Exploring the antibacterial mechanism of host defense peptide mimicking poly(2-oxazoline)s , 2020 .
[2] Runhui Liu,et al. Poly(2-Oxazoline) Based Functional Mimics of Peptides to Eradicate MRSA Infections and Persisters While Alleviating Antimicrobial Resistance. , 2020, Angewandte Chemie.
[3] Runhui Liu,et al. Water Insensitive Synthesis of Poly-β-Peptides with Defined Architecture. , 2020, Angewandte Chemie.
[4] J. Tiller,et al. Telechelic biocidal poly(2-oxazoline)s and polycations , 2019, European Polymer Journal.
[5] Runhui Liu,et al. Host defense peptide mimicking poly-β-peptides with fast, potent and broad spectrum antibacterial activities. , 2019, Biomaterials science.
[6] Runhui Liu,et al. Lithium hexamethyldisilazide initiated superfast ring opening polymerization of alpha-amino acid N-carboxyanhydrides , 2018, Nature Communications.
[7] Zhuxian Zhou,et al. A pH-responsive fragrance release system based on pseudopeptide polymeric micelles , 2018, Reactive and Functional Polymers.
[8] Tim R. Dargaville,et al. Poly(2-oxazoline) Hydrogels: State-of-the-Art and Emerging Applications. , 2018, Macromolecular bioscience.
[9] R. Hoogenboom,et al. The chemistry of poly(2-oxazoline)s ☆ , 2017 .
[10] Peng Sang,et al. γ-AApeptides: Design, Structure, and Applications. , 2016, Accounts of chemical research.
[11] R. Laxminarayan,et al. Access to effective antimicrobials: a worldwide challenge , 2016, The Lancet.
[12] Richard Hoogenboom,et al. Tuning the LCST of poly(2‐cyclopropyl‐2‐oxazoline) via gradient copolymerization with 2‐ethyl‐2‐oxazoline , 2014 .
[13] A. Katritzky,et al. Peptidomimetics via modifications of amino acids and peptide bonds. , 2014, Chemical Society reviews.
[14] J. Tiller,et al. Biologisch schaltbare antimikrobielle Poly(2‐methyloxazoline) auf Grundlage des Satellitengruppeneffekts , 2014 .
[15] A. Sickmann,et al. Antimicrobial poly(2-methyloxazoline)s with bioswitchable activity through satellite group modification. , 2014, Angewandte Chemie.
[16] H. Goossens,et al. Antibiotic resistance—the need for global solutions , 2013, BDJ.
[17] Rongsheng E. Wang,et al. Recent development of small antimicrobial peptidomimetics. , 2012, Future medicinal chemistry.
[18] U. Schubert,et al. Poly(2-ethyl-2-oxazoline) as alternative for the stealth polymer poly(ethylene glycol): comparison of in vitro cytotoxicity and hemocompatibility. , 2012, Macromolecular bioscience.
[19] Renzo M. Paulus,et al. Thermoresponsive poly(2-oxazine)s. , 2012, Macromolecular rapid communications.
[20] Remy Chait,et al. What counters antibiotic resistance in nature? , 2011, Nature chemical biology.
[21] U. Schubert,et al. Multifunctional Poly(2-oxazoline) Nanoparticles for Biological Applications. , 2010, Macromolecular rapid communications.
[22] Richard Hoogenboom. Poly(2‐oxazoline): eine Polymerklasse mit vielfältigen Anwendungsmöglichkeiten , 2009 .
[23] Richard Hoogenboom,et al. Poly(2-oxazoline)s: a polymer class with numerous potential applications. , 2009, Angewandte Chemie.
[24] S. Gellman,et al. Structure-activity relationships among random nylon-3 copolymers that mimic antibacterial host-defense peptides. , 2009, Journal of the American Chemical Society.
[25] W. DeGrado,et al. De novo design and in vivo activity of conformationally restrained antimicrobial arylamide foldamers , 2009, Proceedings of the National Academy of Sciences.
[26] R. Schubert,et al. Insights in the antibacterial action of poly(methyloxazoline)s with a biocidal end group and varying satellite groups. , 2008, Biomacromolecules.
[27] A. Barron,et al. Peptoids that mimic the structure, function, and mechanism of helical antimicrobial peptides , 2008, Proceedings of the National Academy of Sciences.
[28] F. Veronese,et al. Synthesis and characterization of poly(2-ethyl 2-oxazoline)-conjugates with proteins and drugs: suitable alternatives to PEG-conjugates? , 2008, Journal of controlled release : official journal of the Controlled Release Society.
[29] R. Hancock,et al. Antimicrobial and host-defense peptides as new anti-infective therapeutic strategies , 2006, Nature Biotechnology.
[30] J. Tiller,et al. Influence of satellite groups on telechelic antimicrobial functions of polyoxazolines. , 2005, Macromolecular bioscience.
[31] J. Tiller,et al. Poly(oxazoline)s with telechelic antimicrobial functions. , 2005, Biomacromolecules.
[32] M. Zasloff. Antimicrobial peptides of multicellular organisms , 2002, Nature.
[33] M. Litt,et al. Polymerization of cyclic imino ethers. I. Oxazolines , 1967 .
[34] W. Seeliger,et al. Neuere Synthesen und Reaktionen cyclischer Imidsäureester , 1966 .
[35] W. Seeliger,et al. Recent syntheses and reactions of cyclic imidic esters. , 1966, Angewandte Chemie.
[36] D. P. Sheetz,et al. Homopolymerization of 2‐alkyl‐ and 2‐aryl‐2‐oxazolines , 1966 .
[37] K. Fukui,et al. Ring‐opening polymerization of 2‐substituted 2‐oxazolines , 1966 .