Antifungal Polymer Containing Menthoxy Triazine
Source abstract
Abstract
An antifungal polymer containing menthoxy triazine was synthesized by a polycondensation of 2,4-dichloro-6-menthoxy-1,3,5-triazine (DMT) with 4,4-oxidianiline (ODA) and named as P(MT-alt-ODA). To emphasize the antifungal performance of the menthoxy group, series of similar triazine polymers derived correspondingly with hydrogen, ethoxy, and decoxy groups were prepared and served as controls. The spores of Aspergillus niger were used for an antifungal evaluation. Only P(MT-alt-ODA) can effectively inhibit the growth and spread of spores. A further in-depth analysis combined with an inhibition zone and water contact angle illustrated that the surface menthoxy stereochemistry is crucial for the antifungal mechanism.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Synthesis and Characterization of Heterocyclic Compounds · Synthesis and Biological Evaluation · Click Chemistry and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Beijing Laboratory of Biomedical Materials, College of Life Science and Technology, Beijing University of Chemical Technology, Beijing 100029, China
Baotou Research Institute of Rare Earths, Baotou 014030, China
The Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing 100084, China
Funding
National Natural Science Foundation of China
References (30)
Show source-provided references
1. 10.1016/j.foodcont.2019.04.03510.1016/j.foodcont.2019.04.035 ↗
2. 10.1016/j.postharvbio.2019.03.01710.1016/j.postharvbio.2019.03.017 ↗
3. 10.1126/scitranslmed.300440410.1126/scitranslmed.3004404 ↗
4. 10.1038/nrd.2017.4610.1038/nrd.2017.46 ↗
5. 10.1128/CMR.12.2.31010.1128/CMR.12.2.310 ↗
6. 10.3389/fimmu.2019.0152410.3389/fimmu.2019.01524 ↗
7. 10.1038/s41598-020-59750-510.1038/s41598-020-59750-5 ↗
8. 10.1016/j.colcom.2020.10025310.1016/j.colcom.2020.100253 ↗
9. 10.1016/j.colcom.2020.10028010.1016/j.colcom.2020.100280 ↗
10. 10.1021/cm050524410.1021/cm0505244 ↗
11. 10.1063/1.179438110.1063/1.1794381 ↗
12. 10.1016/j.amjmed.2011.11.00110.1016/j.amjmed.2011.11.001 ↗
13. 10.1038/nrmicro117910.1038/nrmicro1179 ↗
14. 10.1002/jsfa.385710.1002/jsfa.3857 ↗
15. 10.1016/j.mycmed.2010.05.00510.1016/j.mycmed.2010.05.005 ↗
16. 10.1002/ptr.207210.1002/ptr.2072 ↗
17. 10.1128/AAC.49.6.2474-2478.200510.1128/AAC.49.6.2474-2478.2005 ↗
18. 10.1016/j.jmst.2020.08.00710.1016/j.jmst.2020.08.007 ↗
19. 10.1016/j.tet.2006.07.03910.1016/j.tet.2006.07.039 ↗
20. 10.1016/j.reactfunctpolym.2013.03.00510.1016/j.reactfunctpolym.2013.03.005 ↗
21. 10.1021/acsmacrolett.5b0063410.1021/acsmacrolett.5b00634 ↗
22. 10.1021/acs.macromol.6b0018110.1021/acs.macromol.6b00181 ↗
23. 10.1002/app.1250010.1002/app.12500 ↗
24. 10.1002/aenm.20160167410.1002/aenm.201601674 ↗
25. Sung J. H. · Korea-Aust Rheol J. · 2004 · 16 · 193
26. 10.1007/s10847-018-0851-810.1007/s10847-018-0851-8 ↗
27. 10.1021/am505481q10.1021/am505481q ↗
28. 10.1016/j.jcis.2016.07.02210.1016/j.jcis.2016.07.022 ↗
29. 10.1007/978-3-030-34475-7_1910.1007/978-3-030-34475-7_19 ↗
30. 10.1016/j.colcom.2020.10033610.1016/j.colcom.2020.100336 ↗