Synthesis, Characterization, and Antibacterial Activity of New Isatin Derivatives

被引:17
作者
Nain, Sumitra [1 ]
Mathur, Garima [1 ]
Anthwal, Tulika [1 ]
Sharma, Swapnil [1 ]
Paliwal, Sarvesh [1 ]
机构
[1] Banasthali Vidyapith, Dept Pharm, Banasthali 304022, Rajasthan, India
关键词
isatin; o-phenylenediamine; chemotherapeutic; amoxicillin; antimicrobial activity; antibacterial; ANTIVIRAL ACTIVITY; ANTIOXIDANT;
D O I
10.1007/s11094-023-02867-4
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
1H-indol-2,3-dione (isatin) class of biologically active compounds have analgesic, anti-microbial, anti-inflammatory, anti-tubercular, anti-proliferative properties, and is also useful for the treatment of SARS-CoV. Schiff bases containing isatin moiety are known to have broad spectrum of biological activities like anti-viral, anti-tubercular, anti-fungal, and anti-bacterial. In this work, several Schiff base derivatives have been synthesized using two methods (synthetic and microwave) by reacting isatin with o-phenylenediamine. The synthesized compounds were structurally characterized and their in-vivo antimicrobial activity was tested against Gram-negative and Gram-positive bacteria using the inhibition zone method. Several newly synthesized isatin derivatives were found effective as antimicrobial agents and showed good potency (compounds 3c, 3d, 6a, 6b, 6d). Compound 3c displayed higher antimicrobial activity than standard drug (Amoxicillin) against Staphylococcus aureus at higher concentration (16 mu g/mL) and against Escherichia coli at lower concentration (1 mu g/mL).
引用
收藏
页码:196 / 203
页数:8
相关论文
共 39 条
[1]   Synthesis, characterization, and antiviral activity of novel fluorinated isatin derivatives [J].
Abbas, Samir Y. ;
Farag, Awatef A. ;
Ammar, Yousry A. ;
Atrees, Abeer A. ;
Mohamed, Aly F. ;
El-Henawy, Ahmed A. .
MONATSHEFTE FUR CHEMIE, 2013, 144 (11) :1725-1733
[2]   Schiff bases of indoline-2,3-dione (isatin) derivatives and nalidixic acid carbohydrazide, synthesis, antitubercular activity and pharmacophoric model building [J].
Aboul-Fadl, Tarek ;
Bin-Jubair, Fayzah A. S. ;
Aboul-Wafa, Omima .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2010, 45 (10) :4578-4586
[3]  
Almutairia S. M., 2017, J MOL STRUCT, P1
[4]  
Alsalihi IE., 2018, ARO, V6, P38
[5]   New isatin derivatives with antioxidant activity [J].
Andreani, Aldo ;
Burnelli, Silvia ;
Granaiola, Massimiliano ;
Leoni, Alberto ;
Locatelli, Alessandra ;
Morigi, Rita ;
Rambaldi, Mirella ;
Varoli, Lucilla ;
Cremonini, Mauro Andrea ;
Placucci, Giuseppe ;
Cervellati, Rinaldo ;
Greco, Emanuela .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2010, 45 (04) :1374-1378
[6]  
[Anonymous], 2014, RACE CLASS
[7]   Methods for in vitro evaluating antimicrobial activity: A review [J].
Balouiri, Mounyr ;
Sadiki, Moulay ;
Koraichi Ibnsouda, Saad .
JOURNAL OF PHARMACEUTICAL ANALYSIS, 2016, 6 (02) :71-79
[8]   THE STRUCTURE AND PROPERTIES OF SOME INDOLIC CONSTITUENTS IN COUROUPITA-GUIANENSIS AUBL [J].
BERGMAN, J ;
LINDSTROM, JO ;
TILSTAM, U .
TETRAHEDRON, 1985, 41 (14) :2879-2881
[9]   Features of the reaction of isatin derivatives with ortho-phenylenediamine [J].
Bogdanov, A. V. ;
Mironov, V. F. .
RUSSIAN JOURNAL OF GENERAL CHEMISTRY, 2015, 85 (10) :2413-2415
[10]   SYNTHESIS AND PHARMACOLOGICAL SCREENING OF NEW ISATIN-3-[N2-(BENZIMIDAZOL-1-ACETYL)]HYDRAZONE [J].
Chaithanya, B. ;
Kasiviswanath, I., V ;
Chary, D. Prabhakara .
BULLETIN OF THE CHEMICAL SOCIETY OF ETHIOPIA, 2019, 33 (02) :321-329