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Dihydropyridine neuropeptide Y Y1 receptor antagonists 2. bioisosteric urea replacements.
Poindexter, Graham S; Bruce, Marc A; Breitenbucher, J Guy; Higgins, Mendi A; Sit, S-Y; Romine, Jeffrey L; Martin, Scott W; Ward, Sally A; McGovern, Rachel T; Clarke, Wendy; Russell, John; Antal-Zimanyi, Ildiko.
Afiliação
  • Poindexter GS; Pharmaceutical Research Institute, Bristol-Myers Squibb Co., 5 Research Parkway, Wallingford, CT 06492-7660, USA. graham.poindexter@bms.com
Bioorg Med Chem ; 12(2): 507-21, 2004 Jan 15.
Article em En | MEDLINE | ID: mdl-14723969
Structure-activity studies around the urea linkage in BMS-193885 (4a) identified the cyanoguanidine moiety as an effective urea replacement in a series of dihydropyridine NPY Y(1) receptor antagonists. In comparison to urea 4a (K(i)=3.3 nM), cyanoguanidine 20 (BMS-205749) displayed similar binding potency at the Y(1) receptor (K(i)=5.1 nM) and full functional antagonism (K(b)=2.6 nM) in SK-N-MC cells. Cyanoguanidine 20 also demonstrated improved permeability properties in Caco-2 cells in comparison to urea 4a (43 vs 19 nm/s).
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ureia / Receptores de Neuropeptídeo Y Limite: Humans Idioma: En Ano de publicação: 2004 Tipo de documento: Article
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ureia / Receptores de Neuropeptídeo Y Limite: Humans Idioma: En Ano de publicação: 2004 Tipo de documento: Article