|1.||Mayur, Y C: 5 articles (03/2013 - 01/2006)|
|2.||Peters, G J: 3 articles (03/2013 - 05/2009)|
|3.||Rajendra Prasad, V V S: 2 articles (03/2013 - 07/2011)|
|4.||Kathmann, Ietje: 2 articles (07/2011 - 11/2009)|
|5.||Lemos, Clara: 2 articles (07/2011 - 11/2009)|
|6.||Prasad, V V S Rajendra: 2 articles (05/2009 - 09/2008)|
|7.||Thimmaiah, Padma: 2 articles (01/2008 - 07/2002)|
|8.||Thimmaiah, Kuntebommanahalli N: 2 articles (01/2008 - 07/2002)|
|9.||Wiench, Benjamin: 1 article (09/2015)|
|10.||Kuete, Victor: 1 article (09/2015)|
12/01/2009 - "A total of seven new oxyranylmethyloxy or thiiranylmethyloxy group substituted 5-azaxanthones and -acridones analogues were synthesized and tested for their biological activities for cancer cell lines and topoisomerases. "
09/01/2008 - "Synthesis of 2-methyl N10-substituted acridones as selective inhibitors of multidrug resistance (MDR) associated protein in cancer cells."
03/01/2013 - "In addition an efficient pharmacophore model was developed from a set of 38 chemosensitizing acridones effective against doxorubicin resistant (HL-60/DX) cancer cell lines. "
09/15/2015 - "In the present study, we investigated the cytotoxicity of five alkaloids including a furoquinoline montrofoline (1) and four acridones namely 1-hydroxy-4-methoxy-10-methylacridone (2), norevoxanthine (3), evoxanthine (4), 1,3-dimethoxy-10-methylacridone (5) against 9 drug-sensitive and multidrug-resistant (MDR) cancer cell lines. "
11/01/2009 - "Synthesis of 2-fluoro N(10)-substituted acridones and their cytotoxicity studies in sensitive and resistant cancer cell lines and their DNA intercalation studies."
|2.||Falciparum Malaria (Plasmodium falciparum Malaria)
11/01/2007 - "A series of novel 10-N-substituted acridones, bearing alkyl side chains with tertiary amine groups at the terminal position, were designed, synthesized, and evaluated for the ability to enhance the potency of quinoline drugs against multidrug-resistant (MDR) Plasmodium falciparum malaria parasites. "
|3.||Liver Neoplasms (Liver Cancer)
01/01/2013 - "The in vitro antibacterial and cytotoxic screening of these acridones reveal that compound 3 has a moderate antibacterial activity (MIC 125 μg/mL) against Micrococcus luteus and Pseudomonas aeruginosa while compound 1 shows a moderate cytotoxic effect (IC50 of 86 μM) against WRL-68 (liver cancer cell line). "
|2.||DNA (Deoxyribonucleic Acid)
|4.||Calmodulin (Calcium-Dependent Activator Protein)
|5.||Vinblastine (Vinblastine Sulfate)
|7.||Multidrug Resistance-Associated Proteins
|10.||3',5'-Cyclic-AMP Phosphodiesterases (3',5' Cyclic Nucleotide Phosphodiesterase)