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Org Biomol Chem ; 2(21): 3162-6, 2004 Nov 07.
Artigo em Inglês | MEDLINE | ID: mdl-15505723

RESUMO

Calix[4]arenes bearing one or two methylenebisphosphonic acid fragments were prepared via addition of diethylphosphite to the parent calix[4]arene aldehydes. The resulting compounds displayed stronger inhibition of calf intestine alkaline phosphatase than simple methylenebisphosphonic or 4-hydroxyphenyl methylenebisphosphonic acids. The action of these phosphorylated calix[4]arenes is concordant with partial mixed-type inhibition. The inhibition constants Ki and Ki' for the calix[4]arene bis(methylenebisphosphonic) acid in Tris-HCl buffer at pH 9 are 0.38 microM and 2.8 microM respectively. The replacement of the phosphoric acid moieties on the macrocycle with diethylphosphonates results in a sharp decrease of its inhibitory action. Preorganizing phosphonic acid fragments using a calixarene platform therefore provides a promising approach for the design of efficient alkaline phosphatase inhibitors.


Assuntos
Fosfatase Alcalina/antagonistas & inibidores , Calixarenos/farmacologia , Intestinos/enzimologia , Organofosfonatos/farmacologia , Fosfatase Alcalina/metabolismo , Animais , Calixarenos/síntese química , Calixarenos/química , Bovinos , Organofosfonatos/síntese química , Organofosfonatos/química
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