Tulp MT - Search Results

1

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: tulp mt. J Med Chem. 1994 Aug 19;37(17):2761-73. doi: 10.1021/jm00043a015. J Med Chem. 1994. PMID: 8064803

2

2-Phenylpyrroles as conformationally restricted benzamide analogues. A new class of potential antipsychotics. 1.

van Wijngaarden I, Kruse CG, van Hes R, van der Heyden JA, Tulp MT. van Wijngaarden I, et al. Among authors: tulp mt. J Med Chem. 1987 Nov;30(11):2099-104. doi: 10.1021/jm00394a028. J Med Chem. 1987. PMID: 2889830

3

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: tulp mt. J Med Chem. 1995 Oct 13;38(21):4303-8. doi: 10.1021/jm00021a020. J Med Chem. 1995. PMID: 7473558

4

N4-unsubstituted N1-arylpiperazines as high-affinity 5-HT1A receptor ligands.

Kuipers W, van Wijngaarden I, Kruse CG, ter Horst-van Amstel M, Tulp MT, IJzerman AP. Kuipers W, et al. Among authors: tulp mt. J Med Chem. 1995 May 26;38(11):1942-54. doi: 10.1021/jm00011a014. J Med Chem. 1995. PMID: 7783126

5

Development of high-affinity 5-HT3 receptor antagonists. Structure-affinity relationships of novel 1,7-annelated indole derivatives.

van Wijngaarden I, Hamminga D, van Hes R, Standaar PJ, Tipker J, Tulp MT, Mol F, Olivier B, de Jonge A. van Wijngaarden I, et al. Among authors: tulp mt. J Med Chem. 1993 Nov 12;36(23):3693-9. doi: 10.1021/jm00075a026. J Med Chem. 1993. PMID: 8246239

6

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: tulp mt. J Med Chem. 1993 Sep 17;36(19):2751-60. doi: 10.1021/jm00071a006. J Med Chem. 1993. PMID: 8410989

7

5-HT1A-versus D2-receptor selectivity of flesinoxan and analogous N4-substituted N1-arylpiperazines.

Kuipers W, Kruse CG, van Wijngaarden I, Standaar PJ, Tulp MT, Veldman N, Spek AL, IJzerman AP. Kuipers W, et al. Among authors: tulp mt. J Med Chem. 1997 Jan 31;40(3):300-12. doi: 10.1021/jm960496o. J Med Chem. 1997. PMID: 9022796

8

The concept of selectivity in 5-HT receptor research.

van Wijngaarden I, Tulp MT, Soudijn W. van Wijngaarden I, et al. Among authors: tulp mt. Eur J Pharmacol. 1990 Jun 12;188(6):301-12. doi: 10.1016/0922-4106(90)90190-9. Eur J Pharmacol. 1990. PMID: 2164935 Review.

9

2-Phenylpyrroles as conformationally restricted benzamide analogues. A new class of potential antipsychotics. 2.

van Wijngaarden I, Kruse CG, van der Heyden JA, Tulp MT. van Wijngaarden I, et al. Among authors: tulp mt. J Med Chem. 1988 Oct;31(10):1934-40. doi: 10.1021/jm00118a011. J Med Chem. 1988. PMID: 2902226

10

Receptor binding profiles of amiloride analogues provide no evidence for a link between receptors and the Na+/H+ exchanger, but indicate a common structure on receptor proteins.

Garritsen A, Ijzerman AP, Tulp MT, Cragoe EJ Jr, Soudijn W. Garritsen A, et al. Among authors: tulp mt. J Recept Res. 1991;11(6):891-907. doi: 10.3109/10799899109064686. J Recept Res. 1991. PMID: 1661335

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