Soudijn W - Search Results

1

1H-imidazo[4,5-c]quinolin-4-amines: novel non-xanthine adenosine antagonists.

van Galen PJ, Nissen P, van Wijngaarden I, IJzerman AP, Soudijn W. van Galen PJ, et al. Among authors: soudijn w. J Med Chem. 1991 Mar;34(3):1202-6. doi: 10.1021/jm00107a046. J Med Chem. 1991. PMID: 2002461

2

Medicinal chemistry of adenosine A1 receptor ligands.

Soudijn W, van Wijngaarden I, IJzerman AP. Soudijn W, et al. Curr Top Med Chem. 2003;3(4):355-67. doi: 10.2174/1568026033392165. Curr Top Med Chem. 2003. PMID: 12570755 Review.

3

Mapping the N6-region of the adenosine A1 receptor with computer graphics.

Van Galen PJ, Leusen FJ, IJzerman AP, Soudijn W. Van Galen PJ, et al. Among authors: soudijn w. Eur J Pharmacol. 1989 Mar 7;172(1):19-27. doi: 10.1016/0922-4106(89)90041-2. Eur J Pharmacol. 1989. PMID: 2714369

4

Influence of the molecular structure of N6-(omega-aminoalkyl)adenosines on adenosine receptor affinity and intrinsic activity.

Pirovano IM, IJzerman AP, Van Galen PJ, Soudijn W. Pirovano IM, et al. Among authors: soudijn w. Eur J Pharmacol. 1989 May 11;172(2):185-93. doi: 10.1016/0922-4106(89)90009-6. Eur J Pharmacol. 1989. PMID: 2767141

5

Adenosine derivatives with N6-alkyl, -alkylamine or -alkyladenosine substituents as probes for the A1-receptor.

van Galen PJ, Ijzerman AP, Soudijn W. van Galen PJ, et al. Among authors: soudijn w. FEBS Lett. 1987 Oct 19;223(1):197-201. doi: 10.1016/0014-5793(87)80535-5. FEBS Lett. 1987. PMID: 2959564 Free article.

6

A series of N4-imidoethyl derivatives of 1-(2,3-dihydro-1,4-benzodioxin-5-yl)piperazine as 5-HT1A receptor ligands: synthesis and structure-affinity relationships.

van Steen BJ, van Wijngaarden I, Tulp MT, Soudijn W. van Steen BJ, et al. Among authors: soudijn w. J Med Chem. 1995 Oct 13;38(21):4303-8. doi: 10.1021/jm00021a020. J Med Chem. 1995. PMID: 7473558

7

Ribose-modified adenosine analogues as potential partial agonists for the adenosine receptor.

van der Wenden EM, von Frijtag Drabbe Künzel JK, Mathôt RA, Danhof M, IJzerman AP, Soudijn W. van der Wenden EM, et al. Among authors: soudijn w. J Med Chem. 1995 Sep 29;38(20):4000-6. doi: 10.1021/jm00020a014. J Med Chem. 1995. PMID: 7562934

8

Novel competitive antagonists for P2 purinoceptors.

van Rhee AM, van der Heijden MP, Beukers MW, IJzerman AP, Soudijn W, Nickel P. van Rhee AM, et al. Among authors: soudijn w. Eur J Pharmacol. 1994 Jun 15;268(1):1-7. doi: 10.1016/0922-4106(94)90114-7. Eur J Pharmacol. 1994. PMID: 7925607

9

Structure-affinity relationship studies on 5-HT1A receptor ligands. 2. Heterobicyclic phenylpiperazines with N4-aralkyl substituents.

van Steen BJ, van Wijngaarden I, Tulp MT, Soudijn W. van Steen BJ, et al. Among authors: soudijn w. J Med Chem. 1994 Aug 19;37(17):2761-73. doi: 10.1021/jm00043a015. J Med Chem. 1994. PMID: 8064803

10

Structure-affinity relationship studies on 5-HT1A receptor ligands. 1. Heterobicyclic phenylpiperazines with N4-alkyl substituents.

van Steen BJ, van Wijngaarden I, Tulp MT, Soudijn W. van Steen BJ, et al. Among authors: soudijn w. J Med Chem. 1993 Sep 17;36(19):2751-60. doi: 10.1021/jm00071a006. J Med Chem. 1993. PMID: 8410989

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