|1.||Stables, J P: 3 articles (11/2006 - 02/2000)|
|2.||Kharya, Murli Dhar: 2 articles (03/2012 - 09/2010)|
|3.||Rajak, Harish: 2 articles (03/2012 - 09/2010)|
|4.||Yogeeswari, Perumal: 2 articles (01/2007 - 08/2004)|
|5.||Sriram, Dharmarajan: 2 articles (01/2007 - 08/2004)|
|6.||Sriram, D: 2 articles (11/2006 - 01/2006)|
|7.||Induja, S: 2 articles (11/2006 - 01/2006)|
|8.||Yogeeswari, P: 2 articles (11/2006 - 01/2006)|
|9.||de Castro, Maria Carolina A B: 1 article (07/2015)|
|10.||Leite, Ana Cristina L: 1 article (07/2015)|
02/01/2000 - "The biological results obtained revealed that in general the acetylhydrazones and semicarbazones afforded good protection against convulsions while the oxamoylhydrazones were significantly less active. "
11/01/2006 - "Two new series of N4-(2, 5-disubstitutedphenyl) semicarbazones were synthesized and evaluated for the anticonvulsant activity in various animal models of seizures. "
01/01/2006 - "The 4-fluorophenyl substituted semicarbazones (5a-5y) emerged as the most potent compounds exhibiting anticonvulsant activity in mouse intraperitoneal (i.p.) and rat per oral (p.o.) MES, scPTZ and psychomotor seizure (6 Hz) screens."
01/01/2011 - "A number of novel 2-(1H-imidazole-1-yl)-1-aryl-substituted ethane-1-one N-substituted phenyl(thio)semicarbazones (1-14) were synthesized to test for their anticonvulsant activity against the two seizure models, maximal electroshock (MES) and subcutaneous pentylenetetrazol (scPTZ). "
06/01/2010 - "A number of N-(4,6-substituted diphenylpyrimidin-2-yl) semicarbazones (4a-t) were synthesized and tested for their anticonvulsant activity against the two seizure models, maximal electroshock seizure (MES) and subcutaneous pentylenetetrazole (scPTZ). "
06/01/1991 - "Studies on antipeptic ulcer agents: the quantitative structure-activity relationship analysis of heterocyclic aldehyde N4-substituted phenyl (thio) semicarbazones."
01/01/1989 - "[Studies on antipeptic ulcer agents: the synthesis and QSAR analysis of heterocycle aldehyde N4-substituted phenyl(thio)semicarbazones]."
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]."
05/01/2010 - "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. "
08/02/2004 - "During the course of our work on the synthesis and screening of new drugs for tuberculosis, we have identified N1-(4-acetamido phenyl)-N4-(2-nitro benzylidene) semicarbazone (1b), which inhibited in vitro Mycobacterium tuberculosis H(37)Rv; 100% inhibition at 1.56 microg/mL. This paper is first of its kind in which aryl semicarbazones are reported to possess antimycobacterials potency greater than p-aminosalicylic acid, ethionamide, ethambutol, ciprofloxacin and kanamycin."
|6.||Aminosalicylic Acid (Rezipas)