ANTINEOPLASTIC ACTIVITY;
ARTICLE;
CELL STRAIN MCF 7;
CONTROLLED STUDY;
DRUG CYTOTOXICITY;
DRUG POTENCY;
DRUG SCREENING;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
IC 50;
IN VITRO STUDY;
PROTON NUCLEAR MAGNETIC RESONANCE;
STRUCTURE ACTIVITY RELATION;
Synthesis, antiprotozoal and anticancer activity of substituted 2-trifluoromethyl-and 2-pentafluoroethylbenzimidazoles
Andrzejewska M, Ye'pez-Mulia L, Cedillo-Rivera R, Tapia A, Vilpo L, Vilpo J, Kazimierczuk Z (2002) Synthesis, antiprotozoal and anticancer activity of substituted 2-trifluoromethyl-and 2-pentafluoroethylbenzimidazoles. Eur J Med Chem 37:973-978
Benzimidazole condensed ring system. IX. Potential antineoplastics. New synthesis of some pyrido[1,2-a]benzimidazoles and related derivatives
Badawey EAM, Kappe T (1995) Benzimidazole condensed ring system. IX. Potential antineoplastics. New synthesis of some pyrido[1,2-a]benzimidazoles and related derivatives. Eur J Med Chem 30:327-332
Benzimidazole condensed ring systems. XI. Synthesis of some cycloalkyl pyrido[l,2-a]benzimidazoles with anticipated antineoplastic activity
Badawey EAM, Kappe T (1999) Benzimidazole condensed ring systems. XI. Synthesis of some cycloalkyl pyrido[l,2-a]benzimidazoles with anticipated antineoplastic activity. Eur J Med Chem 34:663-667
Benzimidazole condensed ring systems. III [1]. Synthesis of some substituted 2,3-dihydrocyclopenta-lH-[4′,5′:2,3]pyrido[, 2-a]benzimidazole-11-carbonitriles
Badawey EAM, Rida SM, Soliman FSG, Kappe T (1989) Benzimidazole condensed ring systems. III [1]. Synthesis of some substituted 2,3-dihydrocyclopenta-lH- [4′,5′:2,3]pyrido[1, 2-a]benzimidazole-11-carbonitriles. Monatsch Chem 120:73-76
Regioselective synthesis of pyrazolo[4,5-g]pyrido[1,2-a] benzimidazoles: Cytotoxic derivatives of pyrido[1,2-a]benzimidazolic ring system
Dupuy M, Pinguet F, Blache Y, Chavignon O, Teulade JC, Chapat JP (1998) Regioselective synthesis of pyrazolo[4,5-g]pyrido[1,2-a] benzimidazoles: cytotoxic derivatives of pyrido[1,2-a]benzimidazolic ring system. Chem Pharm Bull 46:1820-1823
Synthesis and in vitro cytotoxic evaluation of new derivatives of pyrido[1,2-a]benzimidazolic ring system: The pyrido[10,20:1,2]imidazo[4,5-h] quinazolines
Dupuy M, Pinguet F, Chavignon O, Chezal JM, Teulade JC, Chapat JP, Blache Y (2001) Synthesis and in vitro cytotoxic evaluation of new derivatives of pyrido[1,2-a]benzimidazolic ring system: The pyrido[10,20:1,2]imidazo[4,5-h] quinazolines. Chem Pharm Bull 49:1061-1065
Benzimidazole condensed ring systems. XII. Synthesis and anticancer evaluation of certain pyrido[l,2-a]benzimidazole derivatives
EL-Hawash SAM, Badawey EAM, Kappe T (1999) Benzimidazole condensed ring systems. XII. Synthesis and anticancer evaluation of certain pyrido[l,2-a]benzimidazole derivatives. Pharmazie 54:341-346
New transition metal ion complexes with benzimidazole-5-carboxylic acid hydrazides with antitumor activity
Galal SA, Hegab KH, Kassab AS, Rodriguez ML, Kerwin SM, El-Khamry AA, El Diwani HI (2009) New transition metal ion complexes with benzimidazole-5- carboxylic acid hydrazides with antitumor activity. Eur J Med Chem 44:1500-1508
Synthesis and evaluation of intercalating somatostatin receptor binding peptide conjugates for endoradiotherapy
Graham K, Wang Q, Boy RG, Eisenhut M, Haberkorn U, Mier W (2007) Synthesis and evaluation of intercalating somatostatin receptor binding peptide conjugates for endoradiotherapy. J Pharm Pharm Sci 10:286-297
Some fused heterocyclic compounds as eukaryotic topoisomerase II inhibitors
Pinar A, Yurdakul P, Yildiz I, Temiz-Arpaci O, Acan NL, Aki-Sener E, Yalcin I (2004) Some fused heterocyclic compounds as eukaryotic topoisomerase II inhibitors. Biochem Biophys Res Commun 317:670-674
Synthesis and biological activity of certain alkyl 5-(alkoxycarbonyl)-1H- benzimidazole-2-carbamates and related derivatives: A new class of potential antineoplastic and antifilarial agents
Ram S, Wise DS, Wotring LL, McCall JW, Town-send LB (1992) Synthesis and biological activity of certain alkyl 5-(alkoxycarbonyl)-1H-benzimidazole-2- carbamates and related derivatives: a new class of potential antineoplastic and antifilarial agents. J Med Chem 35:539-547
Benzimidazole condensed ring systems. 1. Synthesis and biological investigations of some substituted pyrido [l,2-a]benzimidazoles
Rida SM, Soliman FSG, Badawey EAM, El-Ghazzawi E, Kader O, Kappe T (1988a) Benzimidazole condensed ring systems. 1. Synthesis and biological investigations of some substituted pyrido [l,2-a]benzimidazoles. J Heterocycl Chem 25:1087-1093
Benzimidazole condensed ring systems. 2 [1]. New synthesis of substituted 1-oxo-1H, 5H-pyrido[1,2-a]benzimidazole-4-carbonitriles and related derivatives
Rida SM, Soliman FSG, Badawey EAM, Kappe T (1988b) Benzimidazole condensed ring systems. 2 [1]. New synthesis of substituted 1-oxo-1H, 5H-pyrido[1,2-a]benzimidazole-4-carbonitriles and related derivatives. J Heterocycl Chem 25:1725-1728
Synthesis of substituted 3-hydroxy-1H, 5H-pyrido[1,2-a] -Benzimidazol-1-ones as possible antimicrobial and antineoplastic agents
Soliman FSG, Rida SM, Badawey EAM, Kappe T (1984) Synthesis of substituted 3-hydroxy-1H, 5H-pyrido[1,2-a]-Benzimidazol-1-ones as possible antimicrobial and antineoplastic agents. Arch Pharm 317:951-958
Metabolism of the new anxiolytic agent, a pyrido[1,2-]benzimidazole (PBI) analog (RWJ-53050), in rat and human hepatic S9 fractions, and in dog: Identification of cytochrome p450 isoforms mediated in the human microsomal metabolism
Wu WN, McKown LA, Reitz AB (2006) Metabolism of the new anxiolytic agent, a pyrido[1,2-]benzimidazole (PBI) analog (RWJ-53050), in rat and human hepatic S9 fractions, and in dog: identification of cytochrome p450 isoforms mediated in the human microsomal metabolism. Eur J Drug Metab Pharmacokinet 31: 277-283