SYNTHESIS, CHARACTERIZATION AND BIOLOGICAL EVALUATION OF SOME NOVEL 2-SUBSTITUTED MERCAPTOBENZIMIDAZOLE DERIVATIVES.

被引:0
作者
Reddy, Malladi Srinivas [1 ]
Anisetti, Ravinder Nath [1 ]
Prasad, K. Durga [2 ]
Sannigrahi, Santanu [3 ]
Reddy, P. Arvinda [4 ]
机构
[1] Osmania Univ, Univ Coll Technol, Hyderabad 500007, Andhra Pradesh, India
[2] Natco Res Ctr, Lab 4, Hyderabad, Andhra Pradesh, India
[3] Jadavpur Univ, Dept Pharmaceut Technol, Kolkata 700032, W Bengal, India
[4] CL Baid Metha Coll Pharm, Dept Pharmaceut Chem, Madras 600096, Tamil Nadu, India
关键词
2-mercapto benzimidazole; acid chlorides; anti-ulcer; anti-microbial; HELICOBACTER-PYLORI AGENTS; BENZIMIDAZOLE DERIVATIVES;
D O I
10.1007/s11094-011-0537-7
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Synthesis and biological assessment of six novel 2-substituted mercaptobenzimidazole derivatives is performed. The title compounds are characterized by their analytical and spectral data. All the synthesized compounds are screened for their anti-ulcer and anti-microbial activity. 2-(1H-benzimidazole-2-sulfinyl) -N-(4-benzyloxy-phenyl)-acetamide, N-(4-benzyloxy-phenyl)-4-(1H-benzimidazole-2-sulfinyl)-butyramide, N-(4-benzyloxy phenyl)-4-(5-methoxy 1H-benzimidazole-2-sulfinyl)-butyramide showed significant antiulcer activity. All the compounds moderate antibacterial and antifungal activity.
引用
收藏
页码:642 / 645
页数:4
相关论文
共 19 条
[1]   Synthesis, and antiprotozoal and antibacterial activities of S-substituted 4,6-dibromo- and 4,6-dichloro-2-mercaptobenzimidazoles [J].
Andrzejewska, M ;
Yepez-Mulia, L ;
Tapia, A ;
Cedillo-Rivera, R ;
Laudy, AE ;
Starosciak, BJ ;
Kazimierczuk, Z .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 21 (2-3) :323-329
[2]  
[Anonymous], [No title captured]
[3]  
[Anonymous], [No title captured]
[4]   Synthesis, physicochemical properties and antimicrobial activity of some new benzimidazole derivatives [J].
Ansari, K. F. ;
Lal, C. .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2009, 44 (10) :4028-4033
[5]  
FATMA N, 1988, Indian Journal of Pharmaceutical Sciences, V50, P265
[6]   Benzimidazole 2′-isonucleosides:: Design, synthesis, and antiviral activity of 2-substituted-5,6-dichlorobenzimidazole 2′-isonucleosides [J].
Freeman, GA ;
Selleseth, DW ;
Rideout, JL ;
Harvey, RJ .
NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, 2000, 19 (1-2) :155-174
[7]  
Gillespie S., 1994, MED MICROBIOLOGY ILL
[8]   NOVEL POTENTIAL ANTI-CANCER AGENTS DERIVED FROM BENZIMIDAZOLE [J].
IBRAHIM, ESA ;
OMAR, AMME ;
KHALIL, MA .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1980, 69 (11) :1348-1350
[9]   Antileishmanial activity of the antiulcer agent omeprazole [J].
Jiang, SP ;
Meadows, J ;
Anderson, SA ;
Mukkada, AJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (08) :2569-2574
[10]   Novel structures derived from 2-[[(2-Pyridyl)methyl]thio]-1H-benzimidazole as anti-Helicobacter pylori agents, part 1 [J].
Kühler, TC ;
Swanson, M ;
Christenson, B ;
Klintenberg, AC ;
Lamm, B ;
Fägerhag, J ;
Gatti, R ;
Ölwegård-Halvarsson, M ;
Shcherbuchin, V ;
Elebring, T ;
Sjöström, JE .
JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (19) :4282-4299