Daly JW - Search Results

1

Imidazo[2,1-i]purin-5-ones and related tricyclic water-soluble purine derivatives: potent A(2A)- and A(3)-adenosine receptor antagonists.

Müller CE, Thorand M, Qurishi R, Diekmann M, Jacobson KA, Padgett WL, Daly JW. Müller CE, et al. Among authors: daly jw. J Med Chem. 2002 Aug 1;45(16):3440-50. doi: 10.1021/jm011093d. J Med Chem. 2002. PMID: 12139454 Free PMC article.

2

1,8-disubstituted xanthine derivatives: synthesis of potent A2B-selective adenosine receptor antagonists.

Hayallah AM, Sandoval-Ramírez J, Reith U, Schobert U, Preiss B, Schumacher B, Daly JW, Müller CE. Hayallah AM, et al. Among authors: daly jw. J Med Chem. 2002 Mar 28;45(7):1500-10. doi: 10.1021/jm011049y. J Med Chem. 2002. PMID: 11906291

3

Functionalized congeners of adenosine: preparation of analogues with high affinity for A1-adenosine receptors.

Jacobson KA, Kirk KL, Padgett WL, Daly JW. Jacobson KA, et al. Among authors: daly jw. J Med Chem. 1985 Sep;28(9):1341-6. doi: 10.1021/jm00147a039. J Med Chem. 1985. PMID: 2993623 Free PMC article.

4

Xanthine functionalized congeners as potent ligands at A2-adenosine receptors.

Jacobson KA, Ukena D, Padgett W, Daly JW, Kirk KL. Jacobson KA, et al. Among authors: daly jw. J Med Chem. 1987 Jan;30(1):211-4. doi: 10.1021/jm00384a037. J Med Chem. 1987. PMID: 3806597 Free PMC article.

5

Tetrahydrobenzothiophenone derivatives as a novel class of adenosine receptor antagonists.

van Rhee AM, Siddiqi SM, Melman N, Shi D, Padgett WL, Daly JW, Jacobson KA. van Rhee AM, et al. Among authors: daly jw. J Med Chem. 1996 Jan 19;39(2):398-406. doi: 10.1021/jm9504823. J Med Chem. 1996. PMID: 8558508 Free PMC article.

6

Agonist activity of 2- and 5'-substituted adenosine analogs and their N6-cycloalkyl derivatives at A1- and A2-adenosine receptors coupled to adenylate cyclase.

Daly JW, Padgett WL. Daly JW, et al. Biochem Pharmacol. 1992 Mar 3;43(5):1089-93. doi: 10.1016/0006-2952(92)90616-q. Biochem Pharmacol. 1992. PMID: 1554381

7

7-Deaza-2-phenyladenines: structure-activity relationships of potent A1 selective adenosine receptor antagonists.

Müller CE, Hide I, Daly JW, Rothenhäusler K, Eger K. Müller CE, et al. Among authors: daly jw. J Med Chem. 1990 Oct;33(10):2822-8. doi: 10.1021/jm00172a023. J Med Chem. 1990. PMID: 2213835

8

Binary drugs: conjugates of purines and a peptide that bind to both adenosine and substance P receptors.

Jacobson KA, Lipkowski AW, Moody TW, Padgett W, Pijl E, Kirk KL, Daly JW. Jacobson KA, et al. Among authors: daly jw. J Med Chem. 1987 Aug;30(8):1529-32. doi: 10.1021/jm00391a046. J Med Chem. 1987. PMID: 2441057 Free PMC article.

9

Effects of 8-phenyl and 8-cycloalkyl substituents on the activity of mono-, di-, and trisubstituted alkylxanthines with substitution at the 1-, 3-, and 7-positions.

Shamim MT, Ukena D, Padgett WL, Daly JW. Shamim MT, et al. Among authors: daly jw. J Med Chem. 1989 Jun;32(6):1231-7. doi: 10.1021/jm00126a014. J Med Chem. 1989. PMID: 2724296

10

Sulfur-containing 1,3-dialkylxanthine derivatives as selective antagonists at A1-adenosine receptors.

Jacobson KA, Kiriasis L, Barone S, Bradbury BJ, Kammula U, Campagne JM, Secunda S, Daly JW, Neumeyer JL, Pfleiderer W. Jacobson KA, et al. Among authors: daly jw. J Med Chem. 1989 Aug;32(8):1873-9. doi: 10.1021/jm00128a031. J Med Chem. 1989. PMID: 2754711 Free PMC article.

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