2008
DOI: 10.1002/ardp.200800107
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2‐Sulfonyliminodihydropyrimidines: A Novel Class of Analgesic Compounds

Abstract: A series of 2-sulfonyliminodihydropyrimidine derivatives have been synthesized and evaluated in vivo for their antinociceptive and anti-inflammatory activities. The results were compared with that of acetyl salicylic acid. Compounds 6Ab-d and 6Be displayed an interesting analgesic profile in the acetic acid-induced abdominal contractions test. Based on the results of the carrageenan-hind paw edema test, compound 6Af showed potential anti-inflammatory activity.

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Cited by 6 publications
(2 citation statements)
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“…The product formed was recrystallized in ethanol (1-15). These compounds have already been reported in the following literature [24][25][26][27][28][29][30][31][32] For aliphatic (2-Chloro-acetamides): To a stirring solution of amine in 10 ml dichloromethane, triethylamine was added.…”
Section: General Procedures For the Preparation Of Different Substitutmentioning
confidence: 99%
“…The product formed was recrystallized in ethanol (1-15). These compounds have already been reported in the following literature [24][25][26][27][28][29][30][31][32] For aliphatic (2-Chloro-acetamides): To a stirring solution of amine in 10 ml dichloromethane, triethylamine was added.…”
Section: General Procedures For the Preparation Of Different Substitutmentioning
confidence: 99%
“…A uma solução de 12b (0,100 mg, 0,6 mmol) em acetona (0,6 mL) foi adicionado iodeto de potássio (0,500 mg, 3,0 mmol). A reação ocorreu sob agitação e refluxo em um período de 8 horas, uma vez concluída, o solvente foi removido e o produto recuperado por recristalização em água deionizada (GONZÁLEZROSENDE et al, 2008). A formação do produto desejado foi confirmada através de espectrometria de massas (ESITOF).…”
Section: Síntese Deunclassified