Synthesis, biological activity of newly designed sulfonamide based indole derivative as anti-microbial agent

被引:7
作者
Agrawal, Khushbu [1 ]
Patel, Tarun [1 ]
Patel, Rajeshree [1 ]
机构
[1] Kadi Sarva Vishwavidyalaya, Dept Chem, Gandhinagar, Gujarat, India
关键词
Indole; 1H indole-2-carboxylic acid; Antimicrobial activity; Sulfonamide-based indole derivative; INHIBITORS; MECHANISM;
D O I
10.1186/s43094-023-00466-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BackgroundIn medicinal chemistry, indole and its derivative play an important role. Indole is gaining a lot of importance in medicinal chemistry due to its physiological activity which includes anticancer, antitubercular, antimicrobial, antiviral, antimalarial, anti-inflammatory activities, antileishmanial agents, anti-cholinesterase, and enzyme inhibitory. The spread of antimicrobial resistance becomes a threat to both humans and animals. Antimicrobial resistance has been declared in the top 10 global major health risks by WHO including reported data of 2020 of AMR with 3,106,002 confirmed infections in humans across 70 countries.ResultIn this present work some new sulfonamide-based indole derivatives were synthesized by using 1H-indole -2 carboxylic acid as a starting material. The structure of all synthesized sulfonamide-based indole derivatives was confirmed by 1H NMR and LCMS Spectroscopy.ConclusionAll the synthesized compounds were screened for anti-microbial activity against Gram Positive Staphylococcus aureus, Bacillus megaterium, and Gram Negative Klebsiella pneumonia, Escherichia coli, Salmonellatyphiae, Shigella sp., Enterobacter aerogenes. Among gram-positive Staphylococcus aureus, and Bacillus megaterium. The compound shows activity against Staphylococcus aureus, and among all gram-negative bacteria against Klebsiella pneumonia shows good activity.
引用
收藏
页数:9
相关论文
共 48 条
[1]   Biomimetic amphiphilic chitosan nanoparticles: Synthesis, characterization and antimicrobial activity [J].
Ahmad, Nuraziemah ;
Wee, Chua Eng ;
Wai, Lam Kok ;
Zin, Noraziah Mohamad ;
Azmi, Fazren .
CARBOHYDRATE POLYMERS, 2021, 254
[2]   Design-based synthesis, molecular docking analysis of an anti-inflammatory drug, and geometrical optimization and interaction energy studies of an indole acetamide derivative [J].
Al-Ostoot, Fares Hezam ;
Geetha, D., V ;
Mohammed, Yasser Hussein Eissa ;
Akhileshwari, P. ;
Sridhar, M. A. ;
Khanum, Shaukath Ara .
JOURNAL OF MOLECULAR STRUCTURE, 2020, 1202
[3]   New Isatin-Indole Conjugates: Synthesis, Characterization, and a Plausible Mechanism of Their in vitro Antiproliferative Activity [J].
Al-Wabli, Reem, I ;
Almomen, Aliyah A. ;
Almutairi, Maha S. ;
Keeton, Adam B. ;
Piazza, Gary A. ;
Attia, Mohamed, I .
DRUG DESIGN DEVELOPMENT AND THERAPY, 2020, 14 :483-495
[4]  
Amr AE, 2017, BIOMED RES-INDIA, V28, P75
[5]   New indole and indazole derivatives as potential antimycobacterial agents [J].
Angelova, Violina T. ;
Pencheva, Tania ;
Vassilev, Nikolay ;
Simeonova, Rumyana ;
Momekov, Georgi ;
Valcheva, Violeta .
MEDICINAL CHEMISTRY RESEARCH, 2019, 28 (04) :485-497
[7]  
[Anonymous], 2021, Global Antimicrobial Resistance and Use Surveillance System (GLASS)
[8]  
Arshad M., 2017, Eur. J. Pharm. Med. Res, V4, P511
[9]   Biological evaluation and structure activity relationship of 9-methyl-1-phenyl-9H-pyrido[3,4-b]indole derivatives as anti-leishmanial agents [J].
Ashok, Penta ;
Chander, Subhash ;
Smith, Terry K. ;
Singh, Rajnish Prakash ;
Jha, Prabhat Nath ;
Sankaranarayanan, Murugesan .
BIOORGANIC CHEMISTRY, 2019, 84 :98-105
[10]   Synthesis, antioxidant, and antimicrobial activity of 3-(1H-indole-3-carbonyl)-2H-chromen-2-ones [J].
Basha, Khadhar Navaz Umar ;
Gnanamani, Shanthi ;
Shanmugam, Prakash ;
Venugopal, Sujatha ;
Murthy, Sangeetha ;
Ramasamy, Balagurunathan .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 2021, 58 (10) :2000-2008