TY - JOUR AU - El-Feky, S. A. AU - Thabet, H. K. AU - Ubeid, M. T. PY - 2014 DA - 2014// TI - Synthesis, molecular modeling and anti-inflammatory screening of novel fluorinated quinoline incorporated benzimidazole derivatives using the Pfitzinger reaction JO - J Fluorine Chem VL - 161 UR - https://doi.org/10.1016/j.jfluchem.2014.02.012 DO - 10.1016/j.jfluchem.2014.02.012 ID - El-Feky2014 ER - TY - JOUR AU - Andrzejewskaa, M. AU - Yepez-Mulia, L. AU - Tapia, A. AU - Cedillo-Rivera, R. AU - Laudy, A. E. AU - Starosciak, B. J. AU - Kazimierczuk, Z. PY - 2004 DA - 2004// TI - Synthesis, and antiprotozoal and antibacterial activities of S-substituted 4,6-dibromo- and 4,6-dichloro-2-mercaptobenzimidazoles JO - Eur J Pharm Sci VL - 21 UR - https://doi.org/10.1016/j.ejps.2003.10.024 DO - 10.1016/j.ejps.2003.10.024 ID - Andrzejewskaa2004 ER - TY - JOUR AU - Camacho, J. AU - Barazarte, A. AU - Gamboa, N. AU - Rodrigues, J. AU - Rojas, R. AU - Vaisberg, A. AU - Gilman, R. AU - Charris, J. PY - 2011 DA - 2011// TI - Synthesis and biological evaluation of benzimidazole-5-carbohydrazide derivatives as antimalarial, cytotoxic and antitubercular agents JO - Bioorg Med Chem VL - 19 UR - https://doi.org/10.1016/j.bmc.2011.01.050 DO - 10.1016/j.bmc.2011.01.050 ID - Camacho2011 ER - TY - JOUR AU - Gong, Y. AU - Karakaya, S. S. AU - Guo, X. AU - Zheng, P. AU - Gold, B. AU - Ma, Y. AU - Little, D. AU - Roberts, J. AU - Warrier, T. AU - Jiang, X. AU - Pingle, M. AU - Nathan, C. F. AU - Liu, G. PY - 2014 DA - 2014// TI - Benzimidazole-based compounds kill Mycobacterium tuberculosis JO - Eur J Med Chem VL - 75 UR - https://doi.org/10.1016/j.ejmech.2014.01.039 DO - 10.1016/j.ejmech.2014.01.039 ID - Gong2014 ER - TY - JOUR AU - Abonia, R. AU - Cortes, E. AU - Insuasty, B. AU - Quiroga, J. AU - Nogueras, M. AU - Cobo, J. PY - 2011 DA - 2011// TI - Synthesis of novel 1,2,5-trisubstituted benzimidazoles as potential antitumor agents JO - Eur J Med Chem VL - 46 UR - https://doi.org/10.1016/j.ejmech.2011.06.006 DO - 10.1016/j.ejmech.2011.06.006 ID - Abonia2011 ER - TY - JOUR AU - Fonseca, T. AU - Gigante, B. AU - Marques, M. M. AU - Gilchrist, T. L. AU - Clercq, E. D. PY - 2004 DA - 2004// TI - Synthesis and antiviral evaluation of benzimidazoles, quinoxalines and indoles from dehydroabietic acid JO - Bioorg Med Chem VL - 12 UR - https://doi.org/10.1016/j.bmc.2003.10.013 DO - 10.1016/j.bmc.2003.10.013 ID - Fonseca2004 ER - TY - JOUR AU - Kaur, N. AU - Kaur, A. AU - Bansal, Y. AU - Shah, D. I. AU - Bansal, G. AU - Singh, M. PY - 2008 DA - 2008// TI - Design, synthesis, and evaluation of 5-sulfamoyl benzimidazole derivatives as novel angiotensin II receptor antagonists JO - Bioorg Med Chem VL - 16 UR - https://doi.org/10.1016/j.bmc.2008.10.056 DO - 10.1016/j.bmc.2008.10.056 ID - Kaur2008 ER - TY - JOUR AU - Falco, J. L. AU - Pique, M. AU - Gonzalez, M. AU - Buira, I. AU - Mendez, E. AU - Terencio, J. AU - Perez, C. AU - Princep, M. AU - Palomer, A. AU - Guglietta, A. PY - 2006 DA - 2006// TI - Synthesis, pharmacology and molecular modeling of N-substituted 2-phenyl-indoles and benzimidazoles as potent GABAA agonists JO - Eur J Med Chem VL - 41 UR - https://doi.org/10.1016/j.ejmech.2006.03.031 DO - 10.1016/j.ejmech.2006.03.031 ID - Falco2006 ER - TY - JOUR AU - Ansari, K. F. AU - Lal, C. PY - 2009 DA - 2009// TI - Synthesis, physicochemical properties and antimicrobial activity of some new benzimidazole derivatives JO - Eur J Med Chem VL - 44 UR - https://doi.org/10.1016/j.ejmech.2009.04.037 DO - 10.1016/j.ejmech.2009.04.037 ID - Ansari2009 ER - TY - JOUR AU - Barot, K. P. AU - Manna, K. S. AU - Ghate, M. D. PY - 2017 DA - 2017// TI - Design, synthesis and antimicrobial activities of some novel 1,3,4-thiadiazole, 1,2,4-triazole-5-thione and 1,3-thiazolan-4-one derivatives of benzimidazole JO - J Saudi Chem Soc VL - 21 UR - https://doi.org/10.1016/j.jscs.2013.09.010 DO - 10.1016/j.jscs.2013.09.010 ID - Barot2017 ER - TY - JOUR AU - Desai, N. C. AU - Shihory, N. R. AU - Kotadiya, G. M. PY - 2014 DA - 2014// TI - Facile synthesis of benzimidazole bearing 2-pyridone derivatives as potential antimicrobial agents JO - Chin Chem Lett VL - 25 UR - https://doi.org/10.1016/j.cclet.2013.11.026 DO - 10.1016/j.cclet.2013.11.026 ID - Desai2014 ER - TY - JOUR AU - Ansari, K. F. AU - Lal, C. PY - 2009 DA - 2009// TI - Synthesis and evaluation of some new benzimidazole derivatives as potential antimicrobial agents JO - Eur J Med Chem VL - 44 UR - https://doi.org/10.1016/j.ejmech.2008.01.022 DO - 10.1016/j.ejmech.2008.01.022 ID - Ansari2009 ER - TY - JOUR AU - Arjmand, F. AU - Mohani, B. AU - Ahmad, S. PY - 2005 DA - 2005// TI - Synthesis, antibacterial, antifungal activity and interaction of CT-DNA with a new benzimidazole derived Cu(II) complex JO - Eur J Med Chem VL - 44 UR - https://doi.org/10.1016/j.ejmech.2005.05.005 DO - 10.1016/j.ejmech.2005.05.005 ID - Arjmand2005 ER - TY - JOUR AU - Ayhan-Kilcigil, G. AU - Altanlar, N. PY - 2003 DA - 2003// TI - Synthesis and antimicrobial activities of some new benzimidazole derivatives JO - Il Farmaco VL - 58 UR - https://doi.org/10.1016/S0014-827X(03)00190-3 DO - 10.1016/S0014-827X(03)00190-3 ID - Ayhan-Kilcigil2003 ER - TY - JOUR AU - Bandyopadhyay, P. AU - Sathe, M. AU - Ponmariappan, S. AU - Sharma, A. AU - Sharma, P. AU - Srivastava, A. K. AU - Kaushik, M. P. PY - 2011 DA - 2011// TI - Exploration of in vitro time point quantitative evaluation of newly synthesized benzimidazole and benzothiazole derivatives as potential antibacterial agents JO - Bioorg Med Chem Lett VL - 21 UR - https://doi.org/10.1016/j.bmcl.2011.10.034 DO - 10.1016/j.bmcl.2011.10.034 ID - Bandyopadhyay2011 ER - TY - JOUR AU - Desai, K. G. AU - Desai, K. R. PY - 2006 DA - 2006// TI - Green route for the heterocyclization of -mercaptobenzimidazole into β-lactum segment derivatives containing –CONH– bridge with benzimidazole: screening in vitro antimicrobial activity with various microorganisms JO - Bioorg Med Chem Lett VL - 14 UR - https://doi.org/10.1016/j.bmc.2006.09.017 DO - 10.1016/j.bmc.2006.09.017 ID - Desai2006 ER - TY - JOUR AU - Dolzhenko, A. V. AU - Chui, W. K. AU - Dolzhenko, A. V. AU - Chan, L. W. PY - 2005 DA - 2005// TI - Synthesis and biological activity of fluorinated 2-amino-4-aryl-3,4-dihydro[1, 3, 5]triazino[1,2-a] benzimidazoles JO - J Fluorine Chem VL - 126 UR - https://doi.org/10.1016/j.jfluchem.2005.02.009 DO - 10.1016/j.jfluchem.2005.02.009 ID - Dolzhenko2005 ER - TY - JOUR AU - Goker, H. AU - Ozden, S. AU - Yildiz, S. AU - Boykin, D. W. PY - 2005 DA - 2005// TI - Synthesis and potent antibacterial activity against MRSA of some novel 1,2-disubstituted-1H-benzimidazole-N-alkylated-5-carboxamidines JO - Eur J Med Chem VL - 40 UR - https://doi.org/10.1016/j.ejmech.2005.05.002 DO - 10.1016/j.ejmech.2005.05.002 ID - Goker2005 ER - TY - JOUR AU - Gumus, F. AU - Pamuk, I. AU - Ozden, T. AU - Yildiz, S. AU - Diril, N. AU - Oksuzoglu, E. AU - Gur, S. AU - Ozkul, A. PY - 2003 DA - 2003// TI - Synthesis, characterization and in vitro cytotoxic, mutagenic and antimicrobial activity of platinum (II) complexes with substituted benzimidazole ligands JO - J Inorg Biochem VL - 94 UR - https://doi.org/10.1016/S0162-0134(03)00005-9 DO - 10.1016/S0162-0134(03)00005-9 ID - Gumus2003 ER - TY - JOUR AU - Guven, O. O. AU - Erdogan, T. AU - Goker, H. AU - Yildiz, S. PY - 2007 DA - 2007// TI - Synthesis and antimicrobial activity of some novel phenyl and benzimidazole substituted benzyl ethers JO - Bioorg Med Chem Lett VL - 17 UR - https://doi.org/10.1016/j.bmcl.2007.01.061 DO - 10.1016/j.bmcl.2007.01.061 ID - Guven2007 ER - TY - JOUR AU - Hu, L. AU - Kully, M. L. AU - Boykin, D. W. AU - Abood, N. PY - 2009 DA - 2009// TI - Synthesis and in vitro activity of dicationic bis-benzimidazoles as a new class of anti-MRSA and anti-VRE agents JO - Bioorg Med Chem Lett VL - 19 UR - https://doi.org/10.1016/j.bmcl.2009.01.075 DO - 10.1016/j.bmcl.2009.01.075 ID - Hu2009 ER - TY - JOUR AU - Jardosh, H. H. AU - Sangani, C. B. AU - Patel, M. P. AU - Patel, R. G. PY - 2013 DA - 2013// TI - One step synthesis of pyrido[1,2-a]benzimidazole derivatives of aryloxypyrazole and their antimicrobial evaluation JO - Chin Chem Lett VL - 24 UR - https://doi.org/10.1016/j.cclet.2013.01.021 DO - 10.1016/j.cclet.2013.01.021 ID - Jardosh2013 ER - TY - JOUR AU - Kalinowska-Lis, U. AU - Felczak, A. AU - Checinska, L. AU - Lisowska, K. AU - Ochocki, J. PY - 2014 DA - 2014// TI - Synthesis, characterization and antimicrobial activity of silver (I) complexes of hydroxymethyl derivatives of pyridine and benzimidazole JO - J Organomet Chem VL - 749 UR - https://doi.org/10.1016/j.jorganchem.2013.10.035 DO - 10.1016/j.jorganchem.2013.10.035 ID - Kalinowska-Lis2014 ER - TY - JOUR AU - Kankate, R. S. AU - Gide, P. S. AU - Belsare, D. P. PY - 2015 DA - 2015// TI - Design, synthesis and antifungal evaluation of novel benzimidazole tertiary amine type of fluconazole analogues JO - Arabian J Chem UR - https://doi.org/10.1016/j.arabjc.2015.02.002 DO - 10.1016/j.arabjc.2015.02.002 ID - Kankate2015 ER - TY - JOUR AU - Khalafi-Nezhad, A. AU - Rad, M. N. S. AU - Mohabatkar, H. AU - Asrari, Z. AU - Hemmateenejad, B. PY - 2005 DA - 2005// TI - Design, synthesis, antibacterial and QSAR studies of benzimidazole and imidazole chloroaryloxyalkyl derivatives JO - Bioorg Med Chem Lett VL - 13 UR - https://doi.org/10.1016/j.bmc.2005.01.014 DO - 10.1016/j.bmc.2005.01.014 ID - Khalafi-Nezhad2005 ER - TY - JOUR AU - Klimesova, V. AU - Koci, J. AU - Pour, M. AU - Stachel, J. AU - Waisser, K. AU - Jarmila, K. PY - 2002 DA - 2002// TI - Synthesis and preliminary evaluation of benzimidazole derivatives as antimicrobial agents JO - Eur J Med Chem VL - 37 UR - https://doi.org/10.1016/S0223-5234(02)01342-9 DO - 10.1016/S0223-5234(02)01342-9 ID - Klimesova2002 ER - TY - JOUR AU - Koc, Z. E. AU - Bingol, H. AU - Saf, A. O. AU - Torlak, E. AU - Coskun, A. PY - 2010 DA - 2010// TI - Synthesis of novel tripodal-benzimidazole from 2,4,6-tris(p-formylphenoxy)-1,3,5-triazine: structural, electrochemical and antimicrobial studies JO - J Hazard Mater VL - 183 UR - https://doi.org/10.1016/j.jhazmat.2010.07.018 DO - 10.1016/j.jhazmat.2010.07.018 ID - Koc2010 ER - TY - JOUR AU - Kucukbay, H. AU - Durmaz, R. AU - Orhan, E. AU - Gunal, S. PY - 2003 DA - 2003// TI - Synthesis, antibacterial and antifungal activities of electron-rich olefins derived benzimidazole compounds JO - Il Farmaco VL - 58 UR - https://doi.org/10.1016/S0014-827X(03)00068-5 DO - 10.1016/S0014-827X(03)00068-5 ID - Kucukbay2003 ER - TY - JOUR AU - Kumar, B. V. S. AU - Vaidya, S. D. AU - Kumar, R. V. AU - Bhirud, S. B. AU - Mane, R. B. PY - 2006 DA - 2006// TI - Synthesis and anti-bacterial activity of some novel 2-(6-fluorochroman-2-yl)-1-alkyl/acyl/aroyl-1H-benzimidazoles JO - Eur J Med Chem VL - 41 UR - https://doi.org/10.1016/j.ejmech.2006.01.006 DO - 10.1016/j.ejmech.2006.01.006 ID - Kumar2006 ER - TY - JOUR AU - Kumar, K. AU - Awasthi, D. AU - Lee, S. -. Y. AU - Cummings, J. E. AU - Knudson, S. E. AU - Slayden, R. A. AU - Ojima, I. PY - 2013 DA - 2013// TI - Benzimidazole-based antibacterial agents against Francisella tularensis JO - Bioorg Med Chem VL - 21 UR - https://doi.org/10.1016/j.bmc.2013.02.059 DO - 10.1016/j.bmc.2013.02.059 ID - Kumar2013 ER - TY - JOUR AU - Lopez-Sandoval, H. AU - Londono-Lemos, M. E. AU - Garza-Velasco, R. AU - Poblano-Melendez, I. AU - Granada-Macias, P. AU - Gracia-Mora, I. AU - Barba-Behrens, N. PY - 2008 DA - 2008// TI - Synthesis, structure and biological activities of cobalt(II) and zinc(II) coordination compounds with 2-benzimidazole derivatives JO - J Inorg Biochem VL - 102 UR - https://doi.org/10.1016/j.jinorgbio.2008.01.016 DO - 10.1016/j.jinorgbio.2008.01.016 ID - Lopez-Sandoval2008 ER - TY - JOUR AU - Mehboob, S. AU - Song, J. AU - Hevener, K. E. AU - Su, P. -. C. AU - Boci, T. AU - Brubaker, L. AU - Truong, L. AU - Mistry, T. AU - Deng, J. AU - Cook, J. L. AU - Santarsiero, B. D. AU - Ghosh, A. K. AU - Johnson, M. E. PY - 2015 DA - 2015// TI - Structural and biological evaluation of a novel series of benzimidazole inhibitors of Francisella tularensis enoyl-ACP reductase (FabI) JO - Bioorg Med Chem Lett VL - 25 UR - https://doi.org/10.1016/j.bmcl.2015.01.048 DO - 10.1016/j.bmcl.2015.01.048 ID - Mehboob2015 ER - TY - JOUR AU - Mohamed, G. G. AU - Ibrahim, N. A. AU - Attia, H. A. E. PY - 2009 DA - 2009// TI - Synthesis and antifungicidal activity of some transition metal complexes with benzimidazole dithiocarbamate ligand JO - Spectrochim Acta A VL - 72 UR - https://doi.org/10.1016/j.saa.2008.10.051 DO - 10.1016/j.saa.2008.10.051 ID - Mohamed2009 ER - TY - JOUR AU - Moreira, J. B. AU - Mann, J. AU - Neidle, S. AU - McHugh, T. D. AU - Taylor, P. W. PY - 2013 DA - 2013// TI - Antibacterial activity of head-to-head bis-benzimidazoles JO - Int J Antimicrob Agents VL - 42 UR - https://doi.org/10.1016/j.ijantimicag.2013.04.033 DO - 10.1016/j.ijantimicag.2013.04.033 ID - Moreira2013 ER - TY - JOUR AU - Noolvi, M. AU - Agrawal, S. AU - Patel, H. AU - Badiger, A. AU - Gaba, M. AU - Zambre, A. PY - 2014 DA - 2014// TI - Synthesis, antimicrobial and cytotoxic activity of novel azetidine-2-one derivatives of 1H-benzimidazole JO - Arabian J Chem VL - 7 UR - https://doi.org/10.1016/j.arabjc.2011.02.011 DO - 10.1016/j.arabjc.2011.02.011 ID - Noolvi2014 ER - TY - JOUR AU - Ozden, S. AU - Atabey, D. AU - Yildiz, S. AU - Goker, H. PY - 2005 DA - 2005// TI - Synthesis and potent antimicrobial activity of some novel methyl or ethyl 1H-benzimidazole-5-carboxylates derivatives carrying amide or amidine groups JO - Bioorg Med Chem VL - 13 UR - https://doi.org/10.1016/j.bmc.2004.12.025 DO - 10.1016/j.bmc.2004.12.025 ID - Ozden2005 ER - TY - JOUR AU - Ozkay, Y. AU - Tunali, Y. AU - Karaca, H. AU - Isikdag, I. PY - 2010 DA - 2010// TI - Antimicrobial activity and SAR study of some novel benzimidazole derivatives bearing hydrazone moiety JO - Eur J Med Chem VL - 45 UR - https://doi.org/10.1016/j.ejmech.2010.04.012 DO - 10.1016/j.ejmech.2010.04.012 ID - Ozkay2010 ER - TY - JOUR AU - Padalkar, V. S. AU - Borse, B. N. AU - Gupta, V. D. AU - Phatangare, K. R. AU - Patil, V. S. AU - Umape, P. G. AU - Sekar, N. PY - 2016 DA - 2016// TI - Synthesis and antimicrobial activity of novel 2-substituted benzimidazole, benzoxazole and benzothiazole derivatives JO - Arabian J Chem VL - 9 UR - https://doi.org/10.1016/j.arabjc.2011.12.006 DO - 10.1016/j.arabjc.2011.12.006 ID - Padalkar2016 ER - TY - JOUR AU - Seenaiah, D. AU - Reddy, P. R. AU - Reddy, G. M. AU - Padmaja, A. AU - Padmavathi, V. AU - Siva Krishna, N. PY - 2014 DA - 2014// TI - Synthesis, antimicrobial and cytotoxic activities of pyrimidinyl benzoxazole, benzothiazole and benzimidazole JO - Eur J Med Chem VL - 77 UR - https://doi.org/10.1016/j.ejmech.2014.02.050 DO - 10.1016/j.ejmech.2014.02.050 ID - Seenaiah2014 ER - TY - JOUR AU - Tiwari, A. K. AU - Mishra, A. K. AU - Bajpai, A. AU - Mishra, P. AU - Singh, S. AU - Sinha, D. AU - Singh, V. K. PY - 2007 DA - 2007// TI - Synthesis and evaluation of novel benzimidazole derivative [Bz-Im] and its radio/biological studies JO - Bioorg Med Chem Lett VL - 17 UR - https://doi.org/10.1016/j.bmcl.2007.02.071 DO - 10.1016/j.bmcl.2007.02.071 ID - Tiwari2007 ER - TY - JOUR AU - Tuncbilek, M. AU - Kiper, T. AU - Altanlar, N. PY - 2009 DA - 2009// TI - Synthesis and in vitro antimicrobial activity of some novel substituted benzimidazole derivatives having potent activity against MRSA JO - Eur J Med Chem VL - 44 UR - https://doi.org/10.1016/j.ejmech.2008.06.026 DO - 10.1016/j.ejmech.2008.06.026 ID - Tuncbilek2009 ER - TY - JOUR AU - Zhang, D. AU - Wang, Z. AU - Xu, W. AU - Sun, F. AU - Tang, L. AU - Wang, J. PY - 2009 DA - 2009// TI - Design, synthesis and antibacterial activity of novel actinonin derivatives containing benzimidazole heterocycles JO - Eur J Med Chem VL - 44 UR - https://doi.org/10.1016/j.ejmech.2008.05.009 DO - 10.1016/j.ejmech.2008.05.009 ID - Zhang2009 ER - TY - JOUR AU - Zhang, S. -. L. AU - Damu, G. L. V. AU - Zhang, L. AU - Geng, R. -. X. AU - Zhou, C. -. H. PY - 2012 DA - 2012// TI - Synthesis and biological evaluation of novel benzimidazole derivatives and their binding behavior with bovine serum albumin JO - Eur J Med Chem VL - 55 UR - https://doi.org/10.1016/j.ejmech.2012.07.015 DO - 10.1016/j.ejmech.2012.07.015 ID - Zhang2012 ER - TY - JOUR AU - Zhang, H. -. Z. AU - Damu, G. L. V. AU - Cai, G. -. X. AU - Zhou, C. -. H. PY - 2013 DA - 2013// TI - Design, synthesis and antimicrobial evaluation of novel benzimidazole type of fluconazole analogues and their synergistic effects with chloromycin, norfloxacin and fluconazole JO - Eur J Med Chem VL - 64 UR - https://doi.org/10.1016/j.ejmech.2013.03.049 DO - 10.1016/j.ejmech.2013.03.049 ID - Zhang2013 ER - TY - JOUR AU - Madabhushi, S. AU - Mallu, K. K. R. AU - Vangipuram, V. S. AU - Kurva, S. AU - Poornachandra, Y. AU - Kumar, C. G. PY - 2014 DA - 2014// TI - Synthesis of novel benzimidazole functionalized chiral thioureas and evaluation of their antibacterial and anticancer activities JO - Bioorg Med Chem Lett VL - 24 UR - https://doi.org/10.1016/j.bmcl.2014.08.064 DO - 10.1016/j.bmcl.2014.08.064 ID - Madabhushi2014 ER - TY - JOUR AU - Yadav, S. AU - Lim, S. M. AU - Ramasamy, K. AU - Vasudevan, M. AU - Shah, S. A. A. AU - Mathur, A. AU - Narasimhan, B. PY - 2018 DA - 2018// TI - Synthesis and evaluation of antimicrobial, antitubercular and anticancer activities of 2-(1-benzoyl-1H-benzo[d]imidazol-2-ylthio)-N-substitutedacetamides JO - Chem Cent J VL - 12 UR - https://doi.org/10.1186/s13065-018-0432-3 DO - 10.1186/s13065-018-0432-3 ID - Yadav2018 ER - TY - JOUR AU - Yadav, S. AU - Narasimhan, B. AU - Lim, S. M. AU - Ramasamy, K. AU - Vasudevan, M. AU - Shah, S. A. A. AU - Selvaraj, M. PY - 2017 DA - 2017// TI - Synthesis, characterization, biological evaluation and molecular docking studies of 2-(1H-benzo[d]imidazol-2-ylthio)-N-(substituted-4-oxothiazolidin-3-yl)acetamides JO - Chem Cent J VL - 11 UR - https://doi.org/10.1186/s13065-017-0361-6 DO - 10.1186/s13065-017-0361-6 ID - Yadav2017 ER - TY - JOUR AU - Yadav, S. AU - Narasimhan, B. AU - Lim, S. M. AU - Ramasamy, K. AU - Vasudevan, M. AU - Shah, S. A. A. AU - Mathur, A. PY - 2018 DA - 2018// TI - Synthesis and evaluation of antimicrobial, antitubercular and anticancer activities of benzimidazole derivatives JO - Egypt J Basic Appl Sci VL - 5 UR - https://doi.org/10.1016/j.ejbas.2017.11.001 DO - 10.1016/j.ejbas.2017.11.001 ID - Yadav2018 ER - TY - JOUR AU - Kerimov, I. AU - Ayhan-Kilcigil, G. AU - Can-Eke, B. AU - Altanlar, N. AU - Iscan, M. PY - 2007 DA - 2007// TI - Synthesis, antifungal and antioxidant screening of some novel benzimidazole derivatives JO - J Enzyme Inhib Med Chem VL - 22 UR - https://doi.org/10.1080/14756360701228558 DO - 10.1080/14756360701228558 ID - Kerimov2007 ER - TY - JOUR AU - Si, W. AU - Zhang, T. AU - Li, Y. AU - She, D. AU - Pan, W. AU - Gao, Z. AU - Ning, J. AU - Mei, X. PY - 2016 DA - 2016// TI - Synthesis and biological activity of novel benzimidazole derivatives as potential antifungal agents JO - J Pestic Sci VL - 41 UR - https://doi.org/10.1584/jpestics.D15-037 DO - 10.1584/jpestics.D15-037 ID - Si2016 ER - TY - JOUR AU - Tahlan, S. AU - Narasimhan, B. AU - Lim, S. M. AU - Ramasamy, K. AU - Mani, V. AU - Shah, S. A. A. PY - 2018 DA - 2018// TI - Mercaptobenzimidazole Schiff bases: design, synthesis, antimicrobial studies and anticancer activity on HCT-116 cell line JO - Mini-Rev Med Chem UR - https://doi.org/10.2174/1389557518666181009151008 DO - 10.2174/1389557518666181009151008 ID - Tahlan2018 ER - TY - JOUR AU - Tahlan, S. AU - Narasimhan, B. AU - Lim, S. M. AU - Ramasamy, K. AU - Mani, V. AU - Shah, S. A. A. PY - 2018 DA - 2018// TI - Design, synthesis, SAR study, antimicrobial and anticancer evaluation of novel mercaptobenzimidazole azomethine derivatives JO - Mini-Rev Med Chem UR - https://doi.org/10.2174/1389557518666180903151849 DO - 10.2174/1389557518666180903151849 ID - Tahlan2018 ER - TY - JOUR AU - Yadav, S. AU - Kumar, P. AU - Clercq, E. AU - Balzarini, J. AU - Pannecouque, C. AU - Dewan, S. K. AU - Narasimhan, B. PY - 2010 DA - 2010// TI - 4-[1-(Substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzenesulfonic acids: synthesis, antimicrobial activity, QSAR studies and antiviral evaluation JO - Eur J Med Chem VL - 45 UR - https://doi.org/10.1016/j.ejmech.2010.09.065 DO - 10.1016/j.ejmech.2010.09.065 ID - Yadav2010 ER -