Novel Anti-Microbial Host-Guest Complexes Based on Cationic β-Cyclodextrin Polymers and Triclosan/Butylparaben

2007 ◽  
Vol 28 (23) ◽  
pp. 2244-2248 ◽  
Author(s):  
Yong Guan ◽  
Liying Qian ◽  
Huining Xiao
2018 ◽  
Author(s):  
Diego Alzate-Sanchez ◽  
Yuhan Ling ◽  
Chenjun Li ◽  
Benjamin Frank ◽  
Reiner Bleher ◽  
...  

This manuscript describes cyclodextrin polymers formed as a thin coating on microcrystalline cellulose. The resulting polymer/cellulose composite shows promising performance for removing organic pollutants from water and can be packed into columns for continuous-flow experiments. The polymer/cellulose composite also shows excellent resistance to aerobic and anaerobic biodegradation.


2018 ◽  
Author(s):  
Leilei Xiao ◽  
Casey Ching ◽  
Yuhan Ling ◽  
Mohammadreza Nasiri ◽  
Max Justin Klemes ◽  
...  

This work describes several crosslinked β-cyclodextrin polymer networks and correlates the crosslinker chemistry with binding affinity for per- and polyfluorinated alkyl substances (PFASs), including PFOA and PFOS.


2018 ◽  
Vol 18 (10) ◽  
pp. 855-861
Author(s):  
Rong-Rong Xu ◽  
Rong Hu ◽  
Lin Chen ◽  
Bo Pan ◽  
Xing-Chen Wang ◽  
...  

2014 ◽  
Vol 80 (1-2) ◽  
pp. 101-106 ◽  
Author(s):  
Véronique Wintgens ◽  
Pierre Dubot ◽  
Gisèle Volet ◽  
Bernard Sébille ◽  
Catherine Amiel

2008 ◽  
Vol 68 (1) ◽  
pp. 406-413 ◽  
Author(s):  
Ana Romo ◽  
Francisco Javier Peñas ◽  
José Ramón Isasi ◽  
Iñigo X. García-Zubiri ◽  
Gustavo González-Gaitano

2018 ◽  
Vol 37 (4) ◽  
pp. 771-778 ◽  
Author(s):  
Maurizio Viale ◽  
Rita Tosto ◽  
Valentina Giglio ◽  
Giuseppe Pappalardo ◽  
Valentina Oliveri ◽  
...  

2021 ◽  
Author(s):  
Ankur Sarkar ◽  
Edward Kim ◽  
Taehwan Jang ◽  
Akarawin Hongdusit ◽  
Hyungjun Kim ◽  
...  

Abstract The design of small molecules that inhibit disease-relevant proteins represents a longstanding challenge of medicinal chemistry. Here, we describe an approach for encoding this challenge—the inhibition of a human drug target—into a microbial host and using it to guide the discovery and biosynthesis of targeted, biologically active natural products. This approach identified two previously unknown terpenoid inhibitors of protein tyrosine phosphatase 1B (PTP1B), an elusive therapeutic target for the treatment of diabetes and cancer. Both inhibitors appear to target an allosteric site, which confers selectivity, and can inhibit PTP1B in living cells. A screen of 24 uncharacterized terpene synthases from a pool of 4,464 genes uncovered additional hits, demonstrating a scalable discovery approach, and the incorporation of different PTPs into the microbial host yielded alternative PTP-specific detection systems. Findings illustrate the potential for using microbes to discover and build natural products that exhibit precisely defined biochemical activities yet possess unanticipated structures and/or binding sites.


2013 ◽  
Vol 04 (05) ◽  
pp. 24-29
Author(s):  
Redel Gutierrez ◽  
Niwooti Whangchai ◽  
Nakao Nomura

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