The evaluation of acute toxicity, antimicrobial activity of 1-phenyl-5-p-tolyl-1H-1, 2, 3-triazole, and binding to human serum albumin-Reference-Cited by-同舟云学术

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The evaluation of acute toxicity, antimicrobial activity of 1-phenyl-5-p-tolyl-1H-1, 2, 3-triazole, and binding to human serum albumin

Published:2017-07-17 Issue:11 Volume:31 Page:e21959
ISSN:1095-6670
Container-title:Journal of Biochemical and Molecular Toxicology
language:en
Short-container-title:J Biochem Mol Toxicol

Author:

Duan Hong-Ye¹,Li Jian-Ling¹,Wu Lu-Yong¹,Shu Huo-Ming²,Chen Yu-Xue¹,Ding Guo-Hua¹,Dong Run-Cong³,Si Hong-Zong⁴,Zhong Xia⁵,He Wen-Ying¹^ORCID

Affiliation:

1. Key Laboratory of Tropical Medicinal Plant Chemistry of Ministry of Education; Hainan Normal University; Haikou 571158 People's Republic of China

2. Hainan College of Economics and Business; Haikou 571127 People's Republic of China

3. Research Center for Drug Safety Evaluation of Hainan Province; Haikou 571158 People's Republic of China

4. Institute for Computational Science and Engineering; Qingdao University; Qingdao 266071 People's Republic of China

5. School of Pharmaceutical Science; Hainan Medical University; Haikou 571199 People's Republic of China

Funder

Natural Science Foundation of Hainan Province

National Natural Science Foundation of China

The Science and Technology Plan Projects of Hainan Province of China

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Toxicology,Molecular Biology,Molecular Medicine,Biochemistry,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jbt.21959/fullpdf

Reference57 articles.

1. New click-chemistry methods for 1,2,3-triazoles synthesis: recent advances and applications

2. The growing impact of click chemistry on drug discovery

3. Click Chemistry: 1,2,3-Triazoles as Pharmacophores

4. Indole-2-carboxylic acid derived mono and bis 1,4-disubstituted 1,2,3-triazoles: Synthesis, characterization and evaluation of anticancer, antibacterial, and DNA-cleavage activities

5. Synthesis and biological evaluation of fluconazole analogs with triazole-modified scaffold as potent antifungal agents

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