Click inspired synthesis of p-tert-butyl calix[4]arene tethered benzotriazolyl dendrimers and their evaluation as anti-bacterial and anti-biofilm agents

被引:19
作者
Agrahari, Anand K. [1 ]
Singh, Ashish K. [2 ]
Singh, Anoop S. [1 ]
Singh, Mala [1 ]
Maji, Pathik [3 ]
Yadav, Shivangi [2 ]
Rajkhowa, Sanchayita [4 ]
Prakash, Pradyot [2 ]
Tiwari, Vinod K. [1 ]
机构
[1] Banaras Hindu Univ, Ctr Adv Study, Inst Sci, Dept Chem, Varanasi 221005, Uttar Pradesh, India
[2] Banaras Hindu Univ, Inst Med Sci, Dept Microbiol, Bacterial Biofilm & Drug Resistance Res Lab, Varanasi 221005, Uttar Pradesh, India
[3] Guru Ghasidas Univ, Dept Chem, Bilaspur 495009, India
[4] Jorhat Inst Sci & Technol, Dept Chem, Jorhat 785010, Assam, India
关键词
BIOLOGICAL APPLICATIONS; CALIXARENE; CHEMISTRY; TRIAZOLE; INHIBITORS; NANOPARTICLES; CYCLOADDITION; CYTOTOXICITY; DERIVATIVES; SELECTIVITY;
D O I
10.1039/d0nj02591g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Calixarenes with their three-dimensional structural architecture and ease of functionalization at the upper and/or lower rim are well-known for their plethora of applications in chemical, physical, biological and other disciplines. Herein, CuAAC click inspired p-tert-butylcalix[4]arene tethered benzotriazolyl dendrimers, for example, N-1, N-2 type 2-fold compound 6 and 7 'G(0)' and 6-fold compound 16 and 17 'G(1)' generation benzotriazolyl dendrimer, were devised and also evaluated for their therapeutic potential both in vitro and in vivo. The developed calix[4]arene tethered benzotriazolyl dendrimers have been characterized by standard spectroscopic analysis including NMR (H-1 and C-13), MS, and SEC. Among all the benzotriazolyl dendrimers developed, compound 7 was identified as the effective one which provided potential anti-bacterial and anti-biofilm activities against drug-resistant and slime producing organisms without imparting cytotoxicity to the eukaryotic systems.
引用
收藏
页码:19300 / 19313
页数:14
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