Suliphal Devara Mathada Basavarajaiah, Bennikallu Hire Mathada Mruthyunjayaswamy
Department of Studies and Research in Chemistry, Gulbarga University, Gulbarga-585106, Karnataka, India.
Chem Pharm Bull (Tokyo). 2009 Jun;57(6):557-60. doi: 10.1248/cpb.57.557.
Ethyl 3-oxo-3-{2-[(5-substituted-3-phenyl-1H-indol-2-yl)carbonyl]hydrazinyl}propanoates 5a-b were synthesized according to the literature method. These on further reaction with substituted-2-hydroxy-3-formylquinolines 3a-e yielded 5-substituted-N(beta)-(2-oxo-2H-pyrano[2,3-b]quinoline-3-carbonyl)-3-phenyl-1H-indole-2-carbohydrazides 6a-j. Structures of the all the newly synthesized compounds were confirmed by spectral data. All these compounds have been screened for their antibacterial activity against Staphylococcus aureus, Escherichia coli and Bacillus subtilus, antifungal activity against Aspergillus niger and Candida albicans and antituberculosis activity against Mycobacterium tuberculosis (H37R(v)).
3-氧代-3-{2-[(5-取代-3-苯基-1H-吲哚-2-基)羰基]肼基}丙酸乙酯5a-b按照文献方法合成。这些化合物与取代的2-羟基-3-甲酰基喹啉3a-e进一步反应,得到5-取代-N(β)-(2-氧代-2H-吡喃并[2,3-b]喹啉-3-羰基)-3-苯基-1H-吲哚-2-碳酰肼6a-j。所有新合成化合物的结构均通过光谱数据得以确证。对所有这些化合物针对金黄色葡萄球菌、大肠杆菌和枯草芽孢杆菌的抗菌活性、针对黑曲霉和白色念珠菌的抗真菌活性以及针对结核分枝杆菌(H37R(v))的抗结核活性进行了筛选。