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1.
J Org Chem ; 72(8): 3097-9, 2007 Apr 13.
Artigo em Inglês | MEDLINE | ID: mdl-17355150

RESUMO

The nitrone above is readily available via the intramolecular aza Diels-Alder reaction of an amino acid derived triene in acetic acid. Subsequent treatment of the nitrone in refluxing toluene with substituted actetylenes produced the pictured pyrrole. At lower temperatures a 2,3-dihydroisoxazole, which is the product of a 3+2 dipolar cycloaddition, is produced. Upon heating in refluxing toluene the 2,3-dihydroisoxazole is converted to the pyrrole.


Assuntos
Alcaloides/química , Compostos Azo/química , Compostos Heterocíclicos de 4 ou mais Anéis/química , Tiossemicarbazonas/química , Estrutura Molecular , Pirróis/síntese química , Pirróis/química
2.
Antimicrob Agents Chemother ; 50(1): 230-6, 2006 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-16377691

RESUMO

MurF is a key enzyme in the biosynthesis of the bacterial cell wall in both gram-positive and gram-negative bacteria. This enzyme has not been extensively exploited as a drug target, possibly due to the difficulty in obtaining one of the substrates, UDP-MurNAc-L-Ala-gamma-D-Glu-meso-diaminopimelate, which is usually purified from bacteria. We have identified putative inhibitors of Escherichia coli MurF by a binding assay, thus bypassing the need for substrate. Inhibition of enzymatic activity was demonstrated in a high-performance liquid chromatography-based secondary assay with UDP-MurNAc-L-Ala-gamma-D-Glu-diaminopimelate substrate prepared in a novel way by using muropeptide ligase enzyme to add UDP-MurNAc to synthetic L-Ala-gamma-D-Glu-diaminopimelate; the substrate specificity of muropeptide ligase for peptides containing L-Lys in place of diaminopimelate was also investigated. Using the muropeptide ligase-generated MurF substrate, a thiazolylaminopyrimidine series of MurF enzyme inhibitors with 50% inhibitory concentration values as low as 2.5 microM was identified.


Assuntos
Parede Celular/metabolismo , Inibidores Enzimáticos/isolamento & purificação , Escherichia coli/enzimologia , Peptídeo Sintases/metabolismo , Peptidoglicano/biossíntese , Inibidores Enzimáticos/farmacologia , Escherichia coli/química , Peptídeo Sintases/antagonistas & inibidores
3.
Org Lett ; 6(12): 1931-4, 2004 Jun 10.
Artigo em Inglês | MEDLINE | ID: mdl-15176786

RESUMO

[structure: see text] Intramolecular [4 + 2] cycloaddition using alpha,beta-unsaturated oximes was explored. The reactions proceeded under unusually facile conditions to furnish the nitrones. The latter were subsequently reacted with DMAD to afford [3 + 2] cycloaddition products.


Assuntos
Oximas , Ciclização , Isoxazóis/síntese química , Conformação Molecular , Óxidos de Nitrogênio/química , Oximas/síntese química , Oximas/química
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