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Xanthine mimetics as potent dipeptidyl peptidase IV inhibitors.
Kurukulasuriya, Ravi; Rohde, Jeffrey J; Szczepankiewicz, Bruce G; Basha, Fatima; Lai, Chunqui; Jae, Hwan-Soo; Winn, Martin; Stewart, Kent D; Longenecker, Kenton L; Lubben, Thomas W; Ballaron, Stephen J; Sham, Hing L; von Geldern, Thomas W.
Afiliação
  • Kurukulasuriya R; Metabolic Disease Research, Global Pharmaceutical Research and Development, Abbott Laboratories, 100 Abbott Park Road, Abbott Park, IL 60064-6098, USA. ravi.kurukulasuriya@abbott.com
Bioorg Med Chem Lett ; 16(24): 6226-30, 2006 Dec 15.
Article em En | MEDLINE | ID: mdl-17010607
ABSTRACT
A series of xanthine mimetics containing 5,5 and 5,6 heterocycle fused imidazoles were synthesized as dipeptidyl peptidase IV inhibitors. Compound 7 is potent (h-DPPIV K(i)=2nM) and exhibits excellent selectivity and no species specificity against rat and human enzymes. The X-ray structure confirms that the binding mode of 7 to rat DPPIV is similar to the parent xanthines.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inibidores de Proteases / Xantinas / Inibidores da Dipeptidil Peptidase IV Limite: Animals Idioma: En Revista: Bioorg Med Chem Lett Ano de publicação: 2006 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inibidores de Proteases / Xantinas / Inibidores da Dipeptidil Peptidase IV Limite: Animals Idioma: En Revista: Bioorg Med Chem Lett Ano de publicação: 2006 Tipo de documento: Article