|1.||Singh, Palwinder: 1 article (09/2015)|
|2.||Kaur, Gurcharan: 1 article (09/2015)|
|3.||Sharma, Anuradha: 1 article (09/2015)|
|4.||Kumar, Arun: 1 article (09/2015)|
|5.||Zagni, Chiara: 1 article (03/2014)|
|6.||Rescifina, Antonio: 1 article (03/2014)|
|7.||Pistarà, Venerando: 1 article (03/2014)|
|8.||Corsaro, Antonino: 1 article (03/2014)|
|9.||Varrica, Maria Giulia: 1 article (03/2014)|
|10.||Suryadi, Jimmy: 1 article (09/2012)|
|1.||Chagas Disease (American Trypanosomiasis)
01/01/1999 - "cruzi and in experimental Chagas disease (murine model): alkyllysophospholipids; 5-amino-imidazole-4-carboxamides; bisbenzyl-isoquinolines; cruzipain (crucein) inhibitors; Gossipol; phenothiazines; d) drugs effective in vitro without other reported effects, acridines, actinomycin D, Crystal Violet (gentian violet), diterpenes (Mikania obtusata); N,N'-dimethyl-2-propen-1-amine, epoxidienthiol carbamates, Fe-chelators, guanyl hydrazones, o-naphthoquinones (beta-lapachone); quinoids (miconidine; tingenone); Olivacine, phenazine methosulfate, phenoxi-phenoxyl drugs, Proadifen, pyridinium azolate betaines, sesquiterpenes (Lychophora sp), sesquiterpene lactones, tetrahydrocarbazoles, DL-alpha-trifluoromethylarginine, triphenylmetane dyes. "
|2.||Pancreatic Neoplasms (Pancreatic Cancer)
05/01/2000 - "While the benz[c]acridine derivatives evaluated as part of this study were devoid of topoisomerase poisoning activity, several dihydrobenz[a]acridines were able to enhance DNA cleavage in the presence of topo I. In contrast to certain protoberberine derivatives that did exhibit activity as topo II poisons, none of the benz[a]acridines derivatives enhanced DNA cleavage in the presence of topo II. Among the benz[a]acridines studied, 5,6-dihydro-3,4-methylenedioxy-9,10-dimethoxybenz[a]acridine, 13e, was the most potent topo I poison, with comparable potency to coralyne. "
09/15/2015 - "Identification of amino acid appended acridines as potential leads to anti-cancer drugs."
06/15/2007 - "In order to identify novel anti-cancer drugs, we evaluated the mechanism of action of a novel series of bis- and tetra-acridines. "
01/01/2004 - "The discussed series of compounds is of essential value since acridines belong to the group of natural compounds with the pronounced antibacterial and anti-tumor activity. "
01/01/2004 - "Thus, acridines were used as a basis to create the specific regulatory HIV-1 elements, proliferation inhibitors of leukemia cells and new anti-tumor drugs. "
09/13/2012 - "Potential applications of the chloride-sensitive ester hydrolysis as a self-immolative release mechanism for tumor-selective delivery of platinum-acridines are discussed."
|2.||Coloring Agents (Dyes)
|10.||Gentian Violet (Violet, Crystal)