Design, synthesis of tri-substituted pyrazole derivatives as promising antimicrobial agents and investigation of structure activity relationships

被引:17
作者
Reddy, Guda Mallikarjuna [1 ,2 ]
Garcia, Jarem Raul [2 ]
Yuvaraja, Gutha [3 ]
Subbaiah, Munagapati Venkata [4 ]
Wen, Jet-Chau [4 ,5 ]
机构
[1] Ural Fed Univ, Chem Engn Inst, Ekaterinburg, Russia
[2] Univ Estadual Ponta Grossa, Dept Chem, Ponta Grossa, Parana, Brazil
[3] Guangzhou Univ, Sch Environm Sci & Engn, Guangdong Prov Key Lab Radionuclides Pollut Contr, Guangzhou, Peoples R China
[4] Natl Yunlin Univ Sci & Technol, Res Ctr Soil & Water Resources & Nat Disaster Pre, Touliu, Taiwan
[5] Natl Yunlin Univ Sci & Technol, Dept & Grad Sch Safety & Environm Engn, Touliu, Taiwan
基金
俄罗斯科学基金会;
关键词
UNITED-STATES; ONE-POT; INHIBITORS; ANTIBACTERIAL; PYRANOPYRAZOLES; CARBOXAMIDE; INFECTIONS; LIGANDS; ANALOGS;
D O I
10.1002/jhet.3952
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The major diseases spread in the environment only because of microbes. Even, intensive care units in the hospitals are polluted by microorganisms, particularly, Gram-positive bacteria. Although many antibiotics are existed, there is a need to develop up to date microbial-resistant agents. Hence, the current study aimed to develop prominent antimicrobial drug-related compounds. Thus, a novel series of tri-substituted analogs and their intermediates were synthesized. In addition, total new compounds were screened for their antimicrobial assay and identified as the most efficient biologically active compounds. Moreover, minimal inhibitory antimicrobial activity and appropriate structure activity relationships were investigated. From the results it was observed that, viability of Gram-positive bacteria was most powerfully affected by all active compounds. Finally, this research demonstrated that, these biologically energetic amalgams can be utilized for further preclinical studies with the ambition of standing unique inventive drugs.
引用
收藏
页码:2288 / 2296
页数:9
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