ANTINEOPLASTIC ACTIVITY;
APOPTOSIS;
ARTICLE;
CANCER CELL CULTURE;
CELL PROLIFERATION;
CELL STRAIN K 562;
CELL VIABILITY;
CHEMICAL STRUCTURE;
CONTROLLED STUDY;
CYTOTOXICITY;
DNA FRAGMENTATION;
DRUG SYNTHESIS;
GROWTH INHIBITION;
HUMAN;
HUMAN CELL;
INFRARED RADIATION;
LEUKEMIA CELL;
MASS SPECTROMETRY;
PROTON NUCLEAR MAGNETIC RESONANCE;
Synthesis, antiprotozoal and anticancer activity of substituted 2-trifluoromethyl- and 2-pentafluoroethylbenzimidazoles
DOI 10.1016/S0223-5234(02)01421-6, PII S0223523402014216
M. Andrzejewska L. Yepez-Mulia R. Cedillo-Rivera A. Tapia L. Vilpo J. Vilpo Z. Kazimierczuk 2002 Synthesis, antiprotozoal and anticancer activity of substituted 2-trifluoromethyl and 2-pentafluoroethylbenzimidazoles Eur. J. Med. Chem. 37 973 978 10.1016/S0223-5234(02)01421-6 1:CAS:528:DC%2BD3sXhtV2jsb8%3D 12660022 (Pubitemid 36349006)
Synthesis and in vitro cytotoxic evaluation of novel diazaspiro bicyclo hydantoin derivatives in human leukemia cells: A SAR study
New Drugs, doi:10.1007/s10637-008-9179-3
Ananda Kumar, C. S., Kavitha, C. V., Vinaya, K., Benaka Prasad, S. B., Thimmegowda, N. R., Chandrappa, S., Raghavan, S. C., and Rangappa, K. S., Synthesis and in vitro cytotoxic evaluation of novel diazaspiro bicyclo hydantoin derivatives in human leukemia cells: A SAR study. Invest. New Drugs, doi:10.1007/s10637-008-9179-3. (2008).
Synthesis of 2-(5-((5-(4-chlorophenyl)furan-2-yl)methylene)-4-oxo-2- thioxothiazolidin-3-yl)acetic acid derivatives and evaluation of their cytotoxicity and induction of apoptosis in human leukemia cells
S. Chandrappa C. V. Kavitha M. S. Shahabuddin K. Vinaya C. S. Ananda Kumar S. R. Ranganatha S. C. Raghavan K. S. Rangappa 2009 Synthesis of 2-(5-((5-(4-chlorophenyl)furan-2-yl)methylene)-4-oxo-2-thioxothiazolidin-3-yl) acetic acid derivatives and evaluation of their cytotoxicity and induction of apoptosis in human leukemia cells Bioorg. Med. Chem. 17 2576 2584 10.1016/j.bmc.2009.01.016 1:CAS:528:DC%2BD1MXjsFajsrw%3D 19243955
Synthesis of some new 2-substituted-phenyl-1H-benzimidazole-5- carbonitriles and their potent activity against Candida species
DOI 10.1016/S0968-0896(02)00103-7, PII S0968089602001037
H. Goker C. Kus D. W. Boykin S. Yildiz N. Altanlar 2002 Synthesis of some new 2-substituted-phenyl-1H-benzimidazole-5-carbonitriles and their potent activity against candida species Bioorg. Med. Chem. 10 2589 2596 10.1016/S0968-0896(02)00103-7 1:CAS:528:DC%2BD38XktFygt7Y%3D 12057648 (Pubitemid 34626222)
Synthesis and potent antibacterial activity against MRSA of some novel 1,2-disubstituted-1H-benzimidazole-N-alkylated-5-carboxamidines
DOI 10.1016/j.ejmech.2005.05.002, PII S0223523405001637
H. Goker S. Ozden S. Yýldýz D. W. Boykin 2005 Synthesis and potent antibacterial activity against MRSA of some novel 1,2-disubstituted-1H- benzimidazole-N-alkylated-5-carboxamidines Eur. J. Med. Chem. 40 1062 1069 10.1016/j.ejmech.2005.05.002 15992965 (Pubitemid 41421112)
C. V. Kavitha M. Nambiar C. S. Ananda Kumar B. Choudhary K. Muniyappa K. S. Rangappa S. C. Raghavan 2009 Novel derivatives of spirohydantoin induce growth inhibition followed by apoptosis in leukemia cells Biochem. Pharmacol. 77 348 363 10.1016/j.bcp.2008.10.018 1:CAS:528:DC%2BD1MXhtFCjurk%3D 19014909
The role of protein tyrosine kinases in CYP1A1 induction by omeprazole and thiabendazole in rat hepatocytes
DOI 10.1016/j.lfs.2003.09.056
G. Lemaire C. Delescluse M. Pralavorio N. Ledirac P. Lesca R. Rahmani 2004 The role of protein tyrosine kinases in CYP1A1 induction by omeprazole and thiabendazole in rat hepatocytes Life Sci. 74 2265 2278 10.1016/j.lfs.2003.09. 056 1:CAS:528:DC%2BD2cXhsVOkt7g%3D 14987951 (Pubitemid 38249547)
(2004)Life Sciences, vol.74, Issue.18, pp. 2265-2278
Platinum-based antitumor drugs containing enantiomerically pure α-trifluoromethyl alanine as ligand
DOI 10.1021/jm0504003
N. Margiotta P. Papadia F. Lazzaro M. Crucianelli F. D. Angelis C. Pisano L. Vesci G. Natile 2005 Platinum-based antitumor drugs containing enantiomerically pure alpha-trifluoromethyl alanine as ligand J. Med. Chem. 48 7821 7828 10.1021/jm0504003 1:CAS:528:DC%2BD2MXhtFKgsbnP 16302821 (Pubitemid 41699833)
Synthesis and antitrichinellosis activity of some 2-substituted-[1,3] thiazolo[3,2-a]benzimidazol-3(2H)-ones
DOI 10.1016/j.bmc.2005.06.046, PII S0968089605005742
A. T. Mavrova K. K. Anichina D. I. Vuchev J. A. Tsenov M. S. Kondeva M. K. Micheva 2005 Synthesis and antitrichinellosis activity of some 2-substituted-[1,3]thiazolo[3,2-a]benzimidazol-3(2H)-ones Bioorg. Med. Chem. 13 5550 5559 10.1016/j.bmc.2005.06.046 1:CAS:528:DC%2BD2MXos1ajsrc%3D 16084100 (Pubitemid 41187918)
Synthesis and potent antimicrobial activity of some novel methyl or ethyl 1H-benzimidazole-5-carboxylates derivatives carrying amide or amidine groups
DOI 10.1016/j.bmc.2004.12.025
S. Ozden D. Atabey S. Yildiz H. Goker 2005 Synthesis and potent antimicrobial activity of some novel methyl or ethyl 1H-benzimidazole-5- carboxylates derivatives carrying amide or amidine groups Bioorg. Med. Chem. 13 1587 1597 10.1016/j.bmc.2004.12.025 15698776 (Pubitemid 40215246)
Synthesis and antitumor activity of 1-substituted-2-methyl-5- nitrobenzimidazoles
DOI 10.1016/j.bmc.2006.06.033, PII S0968089606004986
M. M. Ramla M. A. Omar M. Abdel-Momen H. I. El-Khamry El-Diwani 2006 Synthesis and antitumor activity of 1-substituted-2-methyl-5-nitrobenzimidazoles Bioorg. Med. Chem. 14 7324 7332 10.1016/j.bmc.2006.06.033 1:CAS:528: DC%2BD28XpvFGjtLY%3D 16860558 (Pubitemid 44403102)
S. C. Rajski R. M. Williams 1998 DNA cross-linking agents as antitumor drugs Chem. Rev. 98 2723 2795 10.1021/cr9800199 1:CAS:528:DyaK1cXntVeru70%3D 11848977
Synthesis, antiviral and antitumor activity of 2-substituted-5-amidino- benzimidazoles
DOI 10.1016/j.bmc.2007.04.032, PII S0968089607003501
K. Starcevic M. Kralj K. Ester I. Sabol M. Grce K. Pavelic G. Karminski-Zamola 2007 Synthesis, antiviral and antitumor activity of 2-substituted-5-amidino-benzimidazoles Bioorg. Med. Chem. 15 4419 4426 10.1016/j.bmc.2007.04.032 1:CAS:528:DC%2BD2sXlvFSjsrY%3D 17482821 (Pubitemid 46777296)
Viral and host-cell protein kinases enticing antiviral targets and relevance of nucleoside, and viral thymidine, kinases
DOI 10.1016/S0163-7258(99)00004-2, PII S0163725899000042
D. Shugar 1999 Viral and host-cell protein kinases: Enticing antiviral targets and relevance of nucleoside, and viral thymidine, kinases Pharmacol. Ther. 82 315 335 10.1016/S0163-7258(99)00004-2 1:CAS:528:DyaK1MXjvFOhtb4%3D 10454209 (Pubitemid 29255927)
Hit-to-lead studies on benzimidazole inhibitors of ITK: Discovery of a novel class of kinase inhibitors
DOI 10.1016/j.bmcl.2007.04.045, PII S0960894X07004751
R. J. Snow A. Abeywardane S. Campbell J. Lord M. A. Kashem H. H. Khine K. Josephine J. A. Kowalski S. S. Pullen T. Roma G. P. Roth C. R. Sarko N. S. Wilson M. P. Winters J. P. Wolak C. L. Cywin 2007 Hit-to-lead studies on benzimidazole inhibitors of ITK: Discovery of a novel class of kinase inhibitors Bioorg. Med. Chem. Lett. 17 3660 3666 10.1016/j.bmcl.2007.04.045 1:CAS:528:DC%2BD2sXmsFaitb8%3D 17499505 (Pubitemid 46898812)