Morris PE Jr - Search Results

1

Synthesis of labeled BCX-4208, a potent inhibitor of purine nucleoside phosphorylase.

Kamath VP, Juarez-Brambila JJ, Morris PE Jr. Kamath VP, et al. Among authors: morris pe jr. Drug Test Anal. 2009 Mar;1(3):125-7. doi: 10.1002/dta.24. Drug Test Anal. 2009. PMID: 20355185

2

Synthesis of analogs of forodesine HCl, a human purine nucleoside phosphorylase inhibitor-Part I.

Kamath VP, Xue J, Juarez-Brambila JJ, Morris CB, Ganorkar R, Morris PE Jr. Kamath VP, et al. Among authors: morris pe jr. Bioorg Med Chem Lett. 2009 May 15;19(10):2624-6. doi: 10.1016/j.bmcl.2009.04.017. Epub 2009 Apr 9. Bioorg Med Chem Lett. 2009. PMID: 19386498

3

Synthesis of a potent 5'-methylthioadenosine/S-adenosylhomocysteine (MTAN) inhibitor.

Kamath VP, Zhang J, Morris PE Jr, Babu YS. Kamath VP, et al. Among authors: morris pe jr. Bioorg Med Chem Lett. 2006 May 15;16(10):2662-5. doi: 10.1016/j.bmcl.2006.02.029. Epub 2006 Feb 28. Bioorg Med Chem Lett. 2006. PMID: 16504506

4

Synthesis and pharmacokinetic and pharmacodynamic evaluation of the forodesine HCl analog BCX-3040.

Kezar HS 3rd, Kilpatrick JM, Phillips D, Kellogg D, Zhang J, Morris PE Jr. Kezar HS 3rd, et al. Among authors: morris pe jr. Nucleosides Nucleotides Nucleic Acids. 2005;24(10-12):1817-30. doi: 10.1080/15257770500267246. Nucleosides Nucleotides Nucleic Acids. 2005. PMID: 16438050

5

A novel series of potent and selective small molecule inhibitors of the complement component C1s.

Subasinghe NL, Ali F, Illig CR, Jonathan Rudolph M, Klein S, Khalil E, Soll RM, Bone RF, Spurlino JC, DesJarlais RL, Crysler CS, Cummings MD, Morris PE Jr, Kilpatrick JM, Sudhakara Babu Y. Subasinghe NL, et al. Among authors: morris pe jr. Bioorg Med Chem Lett. 2004 Jun 21;14(12):3043-7. doi: 10.1016/j.bmcl.2004.04.034. Bioorg Med Chem Lett. 2004. PMID: 15149641

6

Synthesis of a potent transition-state inhibitor of 5'-deoxy-5'-methylthioadenosine phosphorylase.

Kamath VP, Ananth S, Bantia S, Morris PE Jr. Kamath VP, et al. Among authors: morris pe jr. J Med Chem. 2004 Mar 11;47(6):1322-4. doi: 10.1021/jm030455+. J Med Chem. 2004. PMID: 14998321

7

An Improved Synthesis of 7-Substituted Pyrrolo[3,2-d]pyrimidines.

Elliott AJ, Morris PE Jr, Petty SL, Williams CH. Elliott AJ, et al. Among authors: morris pe jr. J Org Chem. 1997 Nov 14;62(23):8071-8075. doi: 10.1021/jo971062j. J Org Chem. 1997. PMID: 11671913

8

Addition of lithiated 9-deazapurine derivatives to a carbohydrate cyclic imine: convergent synthesis of the aza-C-nucleoside immucillins.

Evans GB, Furneaux RH, Hutchison TL, Kezar HS, Morris PE Jr, Schramm VL, Tyler PC. Evans GB, et al. Among authors: morris pe jr. J Org Chem. 2001 Aug 24;66(17):5723-30. doi: 10.1021/jo0155613. J Org Chem. 2001. PMID: 11511245

9

Inhibitors of the enzyme purine nucleoside phosphorylase as potential therapy for psoriasis.

Morris PE Jr, Omura GA. Morris PE Jr, et al. Curr Pharm Des. 2000 Jun;6(9):943-59. doi: 10.2174/1381612003400083. Curr Pharm Des. 2000. PMID: 10828318 Review.

10

Synthesis and biological activity of a novel class of purine nucleoside phosphorylase inhibitors.

Morris PE Jr, Elliott AJ, Walton SP, Williams CH, Montgomery JA. Morris PE Jr, et al. Nucleosides Nucleotides Nucleic Acids. 2000 Jan-Feb;19(1-2):379-404. doi: 10.1080/15257770008033016. Nucleosides Nucleotides Nucleic Acids. 2000. PMID: 10772722 No abstract available.

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