Synthesis of Some Unique Carbamate Derivatives bearing 2-Furoyl-1-piperazine as a Valuable Therapeutic Agents

被引:8
作者
Abbasi, Muhammad Athar [1 ]
Hussain, Ghulam [1 ]
Aziz-ur-Rehman [1 ]
Siddiqui, Sabahat Zahra [1 ]
Shah, Syed Adnan Ali [2 ,3 ]
Lodhi, Muhammad Arif [4 ]
Khan, Farman Ali [4 ]
Ashraf, Muhammad [5 ]
Qurat-ul-Ain [5 ]
Ahmad, Irshad [6 ]
Malik, Rabia [6 ]
Shahid, Muhammad [7 ]
Mushtaq, Zahid [7 ]
机构
[1] Govt Coll Univ, Dept Chem, Lahore 54000, Pakistan
[2] Univ Teknol MARA, Fac Pharm, Puncak Alam Campus, Bandar Puncak Alam 42300, Selangor Darul, Malaysia
[3] Univ Teknol MARA, Atta ur Rahman Inst Nat Prod Discovery AuRIns, Level 9,FF3,Puncak Alam Campus, Bandar Puncak Alam 42300, Selangor Darul, Malaysia
[4] Abdul Wali Khan Univ, Dept Biochem, Mardan 23200, Pakistan
[5] Islamia Univ Bahawalpur, Dept Chem, Bahawalpur 63100, Pakistan
[6] Islamia Univ Bahawalpur, Dept Pharm, Bahawalpur 63100, Pakistan
[7] Univ Agr Faisalabad, Dept Biochem, Faisalabad 38040, Pakistan
关键词
2-Furoyl-1-piperazine; H-1-NMR; Acetylcholinesterase; Antimicrobial activity; Hemolytic activity; GLUCOSIDASE; SEQUENCE;
D O I
10.17344/acsi.2016.2986
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The aim of the research work was to synthesize different biologically active carbamate derivatives bearing 2-furoyl-1-piperazine and having modest toxicity. The synthesis was completed as a multiple sequence. The structural confirmation of all the synthesized compounds was obtained by EI-MS, IR and H-1-NMR spectral data. The enzyme inhibition and antibacterial potential of the synthesized compounds was evaluated. To find the utility of the prepared compounds as possible therapeutic agents their cytotoxicity was also checked. All the compounds were active against acetylcholinesterase enzyme, especially 12 and 14 showed very good inhibitory potential relative to Eserine, a reference standard. Almost all the compounds showed good activities against both Gram-positive and Gram-negative bacterial strains.
引用
收藏
页码:159 / 169
页数:11
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