Saunders J - Search Results

1

Structure-activity relationships of piperazinebenzylamines as potent and selective agonists of the human melanocortin-4 receptor.

Pontillo J, Tran JA, Arellano M, Fleck BA, Huntley R, Marinkovic D, Lanier M, Nelson J, Parker J, Saunders J, Tucci FC, Jiang W, Chen CW, White NS, Foster AC, Chen C. Pontillo J, et al. Among authors: saunders j. Bioorg Med Chem Lett. 2004 Sep 6;14(17):4417-23. doi: 10.1016/j.bmcl.2004.06.059. Bioorg Med Chem Lett. 2004. PMID: 15357964

2

A novel synthesis of 2-arylpyrrolo[1,2-a]pyrimid-7-ones and their structure-activity relationships as potent GnRH receptor antagonists.

Zhu YF, Wilcoxen K, Saunders J, Guo Z, Gao Y, Connors PJ Jr, Gross TD, Tucci FC, Struthers RS, Reinhart GJ, Xie Q, Chen C. Zhu YF, et al. Among authors: saunders j. Bioorg Med Chem Lett. 2002 Feb 11;12(3):403-6. doi: 10.1016/s0960-894x(01)00780-6. Bioorg Med Chem Lett. 2002. PMID: 11814807

3

A novel synthesis of 7-aryl-8-fluoro-pyrrolo[1,2-a]pyrimid-4-ones as potent, stable GnRH receptor antagonists.

Tucci FC, Zhu YF, Guo Z, Gross TD, Connors PJ Jr, Struthers RS, Reinhart GJ, Wang X, Saunders J, Chen C. Tucci FC, et al. Among authors: saunders j. Bioorg Med Chem Lett. 2002 Dec 2;12(23):3491-5. doi: 10.1016/s0960-894x(02)00745-x. Bioorg Med Chem Lett. 2002. PMID: 12419391

4

Design and structure-activity relationships of 2-alkyl-3-aminomethyl-6-(3-methoxyphenyl)-7-methyl-8-(2-fluorobenzyl)imidazolo[1,2-a]pyrimid-5-ones as potent GnRH receptor antagonists.

Zhu YF, Guo Z, Gross TD, Gao Y, Connors PJ Jr, Struthers RS, Xie Q, Tucci FC, Reinhart GJ, Wu D, Saunders J, Chen C. Zhu YF, et al. Among authors: saunders j. J Med Chem. 2003 Apr 24;46(9):1769-72. doi: 10.1021/jm0205402. J Med Chem. 2003. PMID: 12699396

5

Synthesis and structure-activity relationships of 1-arylmethyl-3-(2-aminopropyl)-5-aryl-6-methyluracils as potent GnRH receptor antagonists.

Guo Z, Zhu YF, Tucci FC, Gao Y, Struthers RS, Saunders J, Gross TD, Xie Q, Reinhart GJ, Chen C. Guo Z, et al. Among authors: saunders j. Bioorg Med Chem Lett. 2003 Oct 6;13(19):3311-5. doi: 10.1016/s0960-894x(03)00620-6. Bioorg Med Chem Lett. 2003. PMID: 12951116

6

Synthesis and structure-activity relationships of 1-arylmethyl-3-(1-methyl-2-amino)ethyl-5-aryl-6-methyluracils as antagonists of the human GnRH Receptor.

Tucci FC, Zhu YF, Guo Z, Gross TD, Connors PJ Jr, Struthers RS, Reinhart GJ, Saunders J, Chen C. Tucci FC, et al. Among authors: saunders j. Bioorg Med Chem Lett. 2003 Oct 6;13(19):3317-22. doi: 10.1016/s0960-894x(03)00619-x. Bioorg Med Chem Lett. 2003. PMID: 12951117

7

Synthesis and structure-activity relationships of thieno[2,3-d]pyrimidine-2,4-dione derivatives as potent GnRH receptor antagonists.

Guo Z, Chen Y, Wu D, Zhu YF, Struthers RS, Saunders J, Xie Q, Chen C. Guo Z, et al. Among authors: saunders j. Bioorg Med Chem Lett. 2003 Oct 20;13(20):3617-22. doi: 10.1016/s0960-894x(03)00746-7. Bioorg Med Chem Lett. 2003. PMID: 14505682

8

Aryl piperazine melanocortin MC4 receptor agonists.

Dyck B, Parker J, Phillips T, Carter L, Murphy B, Summers R, Hermann J, Baker T, Cismowski M, Saunders J, Goodfellow V. Dyck B, et al. Among authors: saunders j. Bioorg Med Chem Lett. 2003 Nov 3;13(21):3793-6. doi: 10.1016/s0960-894x(03)00796-0. Bioorg Med Chem Lett. 2003. PMID: 14552781

9

Synthesis and structure-activity relationships of 1-arylmethyl-5-aryl-6-methyluracils as potent gonadotropin-releasing hormone receptor antagonists.

Guo Z, Zhu YF, Gross TD, Tucci FC, Gao Y, Moorjani M, Connors PJ Jr, Rowbottom MW, Chen Y, Struthers RS, Xie Q, Saunders J, Reinhart G, Chen TK, Bonneville AL, Chen C. Guo Z, et al. Among authors: saunders j. J Med Chem. 2004 Feb 26;47(5):1259-71. doi: 10.1021/jm030472z. J Med Chem. 2004. PMID: 14971906

10

Synthesis and structure-activity relationships of (R)-1-alkyl-3-[2-(2-amino)phenethyl]-5-(2-fluorophenyl)-6-methyluracils as human GnRH receptor antagonists.

Rowbottom MW, Tucci FC, Zhu YF, Guo Z, Gross TD, Reinhart GJ, Xie Q, Struthers RS, Saunders J, Chen C. Rowbottom MW, et al. Among authors: saunders j. Bioorg Med Chem Lett. 2004 May 3;14(9):2269-74. doi: 10.1016/j.bmcl.2004.02.004. Bioorg Med Chem Lett. 2004. PMID: 15081023

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