Novel N6-(substituted-phenylcarbamoyl)adenosine-5'-uronamides as potent agonists for A3 adenosine receptors. | J Med Chem;39(3): 802-6, 1996 Feb 02. | MEDLINE

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Novel N6-(substituted-phenylcarbamoyl)adenosine-5'-uronamides as potent agonists for A3 adenosine receptors.

Baraldi, P G; Cacciari, B; Spalluto, G; Ji, X D; Olah, M E; Stiles, G; Dionisotti, S; Zocchi, C; Ongini, E; Jacobson, K A.

Affiliation

Baraldi PG; Dipartimento di Scienze Farmaceutiche, Università di Ferrara, Italy.

J Med Chem ; 39(3): 802-6, 1996 Feb 02.

Article in En | MEDLINE | ID: mdl-8576924

Subject(s)

Amides/pharmacology; Purinergic P1 Receptor Agonists; Adenylyl Cyclases/metabolism; Amides/metabolism; Animals; Brain/drug effects; Brain/metabolism; CHO Cells; Cricetinae; Male; Rats; Rats, Sprague-Dawley

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Collection: 01-internacional Database: MEDLINE Main subject: Purinergic P1 Receptor Agonists / Amides Limits: Animals Language: En Journal: J Med Chem Journal subject: QUIMICA Year: 1996 Document type: Article Affiliation country: Italy

Search on Google

Collection: 01-internacional Database: MEDLINE Main subject: Purinergic P1 Receptor Agonists / Amides Limits: Animals Language: En Journal: J Med Chem Journal subject: QUIMICA Year: 1996 Document type: Article Affiliation country: Italy