Warrellow G - Search Results

1

Discovery and characterization of 4'-(2-furyl)-N-pyridin-3-yl-4,5'-bipyrimidin-2'-amine (LAS38096), a potent, selective, and efficacious A2B adenosine receptor antagonist.

Vidal B, Nueda A, Esteve C, Domenech T, Benito S, Reinoso RF, Pont M, Calbet M, López R, Cadavid MI, Loza MI, Cárdenas A, Godessart N, Beleta J, Warrellow G, Ryder H. Vidal B, et al. Among authors: warrellow g. J Med Chem. 2007 May 31;50(11):2732-6. doi: 10.1021/jm061333v. Epub 2007 May 1. J Med Chem. 2007. PMID: 17469811

2

Synthesis and structure-activity relationships of novel histamine H1 antagonists: indolylpiperidinyl benzoic acid derivatives.

Fonquerna S, Miralpeix M, Pagès L, Puig C, Cardús A, Antón F, Cárdenas A, Vilella D, Aparici M, Calaf E, Prieto J, Gras J, Huerta JM, Warrellow G, Beleta J, Ryder H. Fonquerna S, et al. Among authors: warrellow g. J Med Chem. 2004 Dec 2;47(25):6326-37. doi: 10.1021/jm0498203. J Med Chem. 2004. PMID: 15566302

3

Synthesis and structure-activity relationships of piperidinylpyrrolopyridine derivatives as potent and selective H1 antagonists.

Fonquerna S, Miralpeix M, Pagès L, Puig C, Cardús A, Antón F, Vilella D, Aparici M, Prieto J, Warrellow G, Beleta J, Ryder H. Fonquerna S, et al. Among authors: warrellow g. Bioorg Med Chem Lett. 2005 Feb 15;15(4):1165-7. doi: 10.1016/j.bmcl.2004.12.008. Bioorg Med Chem Lett. 2005. PMID: 15686934

4

Racemic and chiral sulfoxides as potential prodrugs of the COX-2 inhibitors Vioxx and Arcoxia.

Caturla F, Amat M, Reinoso RF, Córdoba M, Warrellow G. Caturla F, et al. Among authors: warrellow g. Bioorg Med Chem Lett. 2006 Jun 15;16(12):3209-12. doi: 10.1016/j.bmcl.2006.03.052. Epub 2006 Apr 17. Bioorg Med Chem Lett. 2006. PMID: 16616494

5

Racemic and chiral sulfoxides as potential prodrugs of 4-pyrone COX-2 inhibitors.

Caturla F, Amat M, Reinoso RF, Calaf E, Warrellow G. Caturla F, et al. Among authors: warrellow g. Bioorg Med Chem Lett. 2006 Jul 1;16(13):3605-8. doi: 10.1016/j.bmcl.2006.03.101. Epub 2006 May 2. Bioorg Med Chem Lett. 2006. PMID: 16647258

6

N-(pyrimidin-4-yl) and N-(pyridin-2-yl) phenylalanine derivatives as VLA-4 integrin antagonists.

Porter JR, Archibald SC, Brown JA, Childs K, Critchley D, Head JC, Hutchinson B, Parton TA, Robinson MK, Shock A, Warrellow GJ, Zomaya A. Porter JR, et al. Among authors: warrellow gj. Bioorg Med Chem Lett. 2002 Jun 17;12(12):1595-8. doi: 10.1016/s0960-894x(02)00241-x. Bioorg Med Chem Lett. 2002. PMID: 12039570

7

Synthesis and alpha 2-adrenoceptor antagonist activity of some disulfonamidobenzoquinolizines.

Ward TJ, Warrellow GJ, Stirrup JA, Lattimer N, Rhodes KF. Ward TJ, et al. Among authors: warrellow gj. J Med Chem. 1989 Jan;32(1):179-82. doi: 10.1021/jm00121a033. J Med Chem. 1989. PMID: 2562854

8

Discovery and evaluation of N-(triazin-1,3,5-yl) phenylalanine derivatives as VLA-4 integrin antagonists.

Porter JR, Archibald SC, Brown JA, Childs K, Critchley D, Head JC, Hutchinson B, Parton TA, Robinson MK, Shock A, Warrellow GJ, Zomaya A. Porter JR, et al. Among authors: warrellow gj. Bioorg Med Chem Lett. 2002 Jun 17;12(12):1591-4. doi: 10.1016/s0960-894x(02)00237-8. Bioorg Med Chem Lett. 2002. PMID: 12039569

9

Dehydrophenylalanine derivatives as VLA-4 integrin antagonists.

Porter JR, Archibald SC, Brown JA, Childs K, Critchley D, Head JC, Parton TA, Robinson MK, Shock A, Taylor RJ, Warrellow GJ. Porter JR, et al. Among authors: warrellow gj. Bioorg Med Chem Lett. 2003 Mar 10;13(5):805-8. doi: 10.1016/s0960-894x(03)00019-2. Bioorg Med Chem Lett. 2003. PMID: 12617895

10

Discovery and evaluation of potent, tyrosine-based alpha4beta1 integrin antagonists.

Archibald SC, Head JC, Gozzard N, Howat DW, Parton TA, Porter JR, Robinson MK, Shock A, Warrellow GJ, Abraham WM. Archibald SC, et al. Among authors: warrellow gj. Bioorg Med Chem Lett. 2000 May 1;10(9):997-9. doi: 10.1016/s0960-894x(00)00147-5. Bioorg Med Chem Lett. 2000. PMID: 10853677

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