|1.||Boily, Jean-François: 2 articles (09/2014 - 09/2014)|
|2.||Ramstedt, Madeleine: 2 articles (09/2014 - 09/2014)|
|3.||Hakobyan, Shoghik: 2 articles (09/2014 - 09/2014)|
|4.||Khetmalas, Madhukar: 2 articles (07/2014 - 05/2012)|
|5.||Padhye, Subhash: 2 articles (07/2014 - 05/2012)|
|6.||Ahmad, Aamir: 2 articles (07/2014 - 05/2012)|
|7.||Deshpande, Jyoti: 2 articles (07/2014 - 05/2012)|
|8.||Dandawate, Prasad: 2 articles (07/2014 - 05/2012)|
|9.||Stables, James P: 2 articles (03/2003 - 08/2002)|
|10.||Orun, Oya: 1 article (10/2015)|
01/01/2012 - "Among the synthesized bis(indolyl)hydrazide-hydrazones, the compound 5b with N-(p-chlorobenzyl) and bromo substituents was found to be the most potent against multiple cancer cell lines (IC(50)=1.0 μM, MDA-MB-231). "
10/29/2014 - "Here we aim to study the possible effects of two novel nicotinoyl hydrazones on Human papillomavirus (HPV) infected cervical cancers. "
01/01/2015 - "Synthesis, Characterization, and Anti-Cancer Activity of Some New N'-(2-Oxoindolin-3-ylidene)-2-propylpentane hydrazide-hydrazones Derivatives."
01/01/2012 - "A series of bis(indolyl) hydrazide-hydrazones 5a-n were synthesized and evaluated for their cytotoxicity against selected human cancer cell lines. "
12/15/2011 - "Using a high throughput screen designed to detect inhibitors of Wnt/β-catenin signaling, we identified a series of acyl hydrazones that act downstream of the β-catenin destruction complex to inhibit both Wnt-induced and cancer-associated constitutive Wnt signaling via destabilization of β-catenin. "
|2.||Chagas Disease (American Trypanosomiasis)
10/30/2014 - "Together, these data present a novel series of thiazolyl hydrazones with potential effects against Chagas disease and they could be important leads in continuing development against Chagas disease. "
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. "
01/01/1985 - "In in vitro short-term (3 h) assays, the beta-chloroethyl-methyl-hydrazones B 1 and B 2 inhibit the uptake of 3H-thymidine by EAC and L 1210 leukemia cells, B 2 being 5 to 10 times more effective than B 1. The growth inhibitory effect of both compounds was also confirmed in long-term (7 days) clonal assays using agar-containing glass capillaries, B 2 again being more effective than B 1. In contrast to these differences in vitro, in vivo both substances showed remission to the same degree in EAC- and complete resistance in L 1210-bearing mice. "
01/01/1990 - "Studies on antipeptic ulcer agents: a structure-activity relationship analysis of aldehyde semicarbazones and aryl hydrazones."
01/01/1989 - "[Studies on antipeptic ulcer agents: the synthesis and structure-activity relationship analysis of heterocycle aldehyde (thio) semicarbazones and acyl hydrazones]."
05/01/2012 - "In this work the anti-tuberculosis activity of an in-house series of pyrrole hydrazones was investigated by quantitative structure-activity relationships (QSAR) analysis and by pharmacophore modelling. "
05/01/2012 - "Preliminary investigations of our research team have shown that some pyrrole hydrazones posses strong inhibitory activity against the tuberculosis bacilli, and thus represent a new perspective for development of anti-tuberculosis agents. "
05/01/2012 - "Structure-activity relationships of pyrrole hydrazones as new anti-tuberculosis agents."
01/01/1954 - "[New drugs in the treatment of tuberculosis, hydrazides and hydrazones]."
05/01/2010 - "The aim of this study was to identify a candidate drug for the development of anti-tuberculosis therapy from previously synthesized compounds based on the thiosemicarbazones, semicarbazones, dithiocarbazates and hydrazide/hydrazones compounds. "
|8.||Gentian Violet (Violet, Crystal)
|9.||Coloring Agents (Dyes)
|2.||Drug Therapy (Chemotherapy)