Derivatives of benzimidazole pharmacophore: Synthesis, anticonvulsant, antidiabetic and DNA cleavage studies
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Schmidt, 2005, Epilepsia, 46, 858, 10.1111/j.1528-1167.2005.54904.x
Thiry, 2007, Curr. Top. Med. Chem., 7, 855, 10.2174/156802607780636726
Keane, 2003, Kidney Int., 63, 1499, 10.1046/j.1523-1755.2003.00885.x
Cusi, 1998, Diabetes Rev., 6, 89
Erkkila, 1999, Chem. Rev., 99, 2777, 10.1021/cr9804341
Metcalfe, 2003, Chem. Soc. Rev., 32, 215, 10.1039/b201945k
Chifotides, 2005, Acc. Chem. Res., 38, 146, 10.1021/ar0302078
Mitic, 2006, Chem. Rev., 106, 3338, 10.1021/cr050318f
Yang, 2006, Mol. Cells, 22, 5, 10.1016/j.molcel.2006.03.013
Vos, 2006, Dalton Trans., 41, 4869, 10.1039/b606490f
Hannon, 2007, Chem. Soc. Rev., 36, 280, 10.1039/B606046N
Singh, 1981, Chem. Rev., 81, 175, 10.1021/cr00042a003
Verma, 2008, Eur. J. Med. Chem., 43, 897, 10.1016/j.ejmech.2007.07.017
Nesynov, 1964, Russ. Chem. Rev., 33, 508, 10.1070/RC1964v033n10ABEH001476
Desai, 2005, J. Saudi. Chem. Soc., 9, 631
Mullican, 1993, J. Med. Chem., 36, 1090, 10.1021/jm00060a017
Ersmark, 2005, J. Med. Chem., 48, 6090, 10.1021/jm050463l
Macaev, 2005, Bioorg. Med. Chem., 13, 4842, 10.1016/j.bmc.2005.05.011
El-Emam, 2004, Bioorg. Med. Chem., 12, 5107, 10.1016/j.bmc.2004.07.033
Hosamani, 2008, Can. J. Chem., 86, 1030, 10.1139/v08-152
Shingalapur, 2009, Eur. J. Med. Chem., 44, 4244, 10.1016/j.ejmech.2009.05.021
Reddy, 2009, Arch. Pharm. Chem. Life Sci., 342, 412, 10.1002/ardp.200900022
Hosamani, 2009, J. Enz. Inhib. Med. Chem., 24, 1095, 10.1080/14756360802632716
Keri, 2009, Eur. J. Med. Chem., 44, 5123, 10.1016/j.ejmech.2009.09.011
Barreca, 2001, Bioorg. Med. Chem. Lett., 11, 1793, 10.1016/S0960-894X(01)00304-3
Kulkarni, 1981, Arch. Int. Pharmacodyn, 252, 124
Maroo, 2003, Phytomedicine, 196, 10.1078/094471103321659933
Hemalatha, 2006, Indian J. Trad. Knowledge V, IV, 468
Latha, 2004, Braz. J. Med. Biol. Res., 37, 579, 10.1590/S0100-879X2004000400015
Brown, 1990, Mol. Biol. A Pract Approach, 1, 51