Structure-activity relationships of uridine 5'-diphosphate analogues at the human P2Y6 receptor.

Besada, Pedro; Shin, Dae Hong; Costanzi, Stefano; Ko, Hyojin; Mathé, Christophe; Gagneron, Julien; Gosselin, Gilles; Maddileti, Savitri; Harden, T Kendall; Jacobson, Kenneth A

Besada, Pedro; Shin, Dae Hong; Costanzi, Stefano; Ko, Hyojin; Mathé, Christophe; Gagneron, Julien; Gosselin, Gilles; Maddileti, Savitri; Harden, T Kendall; Jacobson, Kenneth A.

Affiliation

Besada P; Molecular Recognition Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.

J Med Chem ; 49(18): 5532-43, 2006 Sep 07.

Article in En | MEDLINE | ID: mdl-16942026

Subject(s)

Receptors, Purinergic P2/drug effects; Uridine Diphosphate/analogs & derivatives; Uridine Diphosphate/chemical synthesis; Cell Line, Tumor; Humans; Models, Molecular; Purinergic P2 Receptor Agonists; Stereoisomerism; Structure-Activity Relationship; Uridine Diphosphate/pharmacology

Fulltext

XML

PubMed Links

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Uridine Diphosphate / Receptors, Purinergic P2 Type of study: Prognostic_studies Limits: Humans Language: En Journal: J Med Chem Journal subject: QUIMICA Year: 2006 Type: Article Affiliation country: United States

Fulltext

XML

PubMed Links

Search on Google