Literature DB >> 3689436

Biochemical characterization of the antagonist actions of the xanthines, PACPX (1,3-dipropyl-8(2-amino-4-chloro)phenylxanthine) and 8-PT (8-phenyltheophylline) at adenosine A1 and A2 receptors in rat brain tissue.

M Williams1, M F Jarvis, M A Sills, J W Ferkany, A Braunwalder.   

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Year:  1987        PMID： 3689436     DOI： 10.1016/0006-2952(87)90476-x

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN： 0006-2952            Impact factor:   5.858


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  3 in total

1.  Analysis of agonist-antagonist interactions at A1 adenosine receptors.

Authors:  E Leung; K A Jacobson; R D Green
Journal:  Mol Pharmacol       Date:  1990-07       Impact factor: 4.436

2.  1,3,8- and 1,3,7-substituted xanthines: relative potency as adenosine receptor antagonists at the frog neuromuscular junction.

Authors:  A M Sebastião; J A Ribeiro
Journal:  Br J Pharmacol       Date:  1989-01       Impact factor: 8.739

3.  Characterization of the adenosine receptors of the rat superior cervical ganglion.

Authors:  G P Connolly; T W Stone; F Brown
Journal:  Br J Pharmacol       Date:  1993-10       Impact factor: 8.739
  3 in total

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