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1.
J Enzyme Inhib Med Chem ; 21(1): 113-8, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16570514

ABSTRACT

Some 1,5-diaryl-3-ethoxycarbonyl-2-methylpyrrole derivatives were obtained by reacting 1-aryl-3-ethoxycarbonylpent-1,4-diones and a suitable aniline derivative or sulfanilamide under Paal-Knorr pyrrole synthesis conditions. The cytotoxicity of the compounds was tested and all compounds, except for compound 2 h, showed a time-dependent increase in cytotoxic activity. Analgesic activities of the compounds were determined by using the tail-flick and tail-immersion methods; some of the compounds showed potent analgesic activity.


Subject(s)
Analgesics , Cell Proliferation/drug effects , Pyrroles , Tail/drug effects , Analgesics/chemical synthesis , Analgesics/chemistry , Analgesics/pharmacology , Animals , Cells, Cultured , Embryo, Mammalian/cytology , Embryo, Mammalian/drug effects , Female , Fibroblasts/cytology , Fibroblasts/drug effects , Male , Mice , Pyrroles/chemical synthesis , Pyrroles/chemistry , Pyrroles/pharmacology , Rats
2.
Eur J Med Chem ; 41(5): 651-6, 2006 May.
Article in English | MEDLINE | ID: mdl-16554110

ABSTRACT

In this study, some aryl [3-(imidazol-1-yl/triazol-1-ylmethyl)benzofuran-2-yl] ketones, aryl (3-methyl-benzofuran-2-yl) ketoximes and aryl [3-(imidazol-1-yl/triazol-1-ylmethyl)benzofuran-2-yl] ketoximes were synthesised starting from 2-aryloyl-3-methyl-benzofuranes. The structure elucidation of the compounds was performed by IR, 1H-NMR, MASS spectroscopy and elemental analyses. Antifungal activities of the compounds were examined and moderate activity was obtained.


Subject(s)
Antifungal Agents/chemical synthesis , Antifungal Agents/pharmacology , Azoles/chemistry , Benzofurans/chemistry , Imidazoles/chemistry , Oximes/chemistry , Oximes/pharmacology , Antifungal Agents/chemistry , Candida/drug effects , Methylation , Molecular Structure , Oximes/chemical synthesis , Structure-Activity Relationship
3.
Arch Pharm Res ; 26(3): 202-6, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12723932

ABSTRACT

In this study, some aryl (3-methyl-benzofuran-2-yl) ketoximes and their ethers and esters were synthesised. The structure elucidation of the compounds was performed by IR, 1H-NMR, MASS spectroscopy and elemental analyses. Antifungal activities of the compounds were examined and moderate activity was obtained.


Subject(s)
Antifungal Agents/chemical synthesis , Benzofurans/chemical synthesis , Oximes/chemical synthesis , Antifungal Agents/pharmacology , Benzofurans/pharmacology , Microbial Sensitivity Tests/statistics & numerical data , Oximes/pharmacology
4.
Farmaco ; 57(7): 609-12, 2002 Jul.
Article in English | MEDLINE | ID: mdl-12164223

ABSTRACT

In this study, some aryl(benzofuran-2-yl)ketoximes and their ethers and esters were synthesised. The structure elucidation of the compounds was performed by IR, 1H NMR and mass spectroscopic data and elemental analyses results. Antifungal activities of the compounds were examined and notable activity was obtained.


Subject(s)
Antifungal Agents/chemical synthesis , Antifungal Agents/pharmacology , Benzofurans/chemical synthesis , Benzofurans/pharmacology , Candida albicans/drug effects , Oximes/chemical synthesis , Oximes/pharmacology , Antifungal Agents/chemistry , Benzofurans/chemistry , Magnetic Resonance Spectroscopy , Microbial Sensitivity Tests , Oximes/chemistry
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