Yates M - Search Results

1

Thienopyridine urea inhibitors of KDR kinase.

Heyman HR, Frey RR, Bousquet PF, Cunha GA, Moskey MD, Ahmed AA, Soni NB, Marcotte PA, Pease LJ, Glaser KB, Yates M, Bouska JJ, Albert DH, Black-Schaefer CL, Dandliker PJ, Stewart KD, Rafferty P, Davidsen SK, Michaelides MR, Curtin ML. Heyman HR, et al. Among authors: yates m. Bioorg Med Chem Lett. 2007 Mar 1;17(5):1246-9. doi: 10.1016/j.bmcl.2006.12.015. Epub 2006 Dec 9. Bioorg Med Chem Lett. 2007. PMID: 17188869

2

Isothiazolopyrimidines and isoxazolopyrimidines as novel multi-targeted inhibitors of receptor tyrosine kinases.

Ji Z, Ahmed AA, Albert DH, Bouska JJ, Bousquet PF, Cunha GA, Glaser KB, Guo J, Li J, Marcotte PA, Moskey MD, Pease LJ, Stewart KD, Yates M, Davidsen SK, Michaelides MR. Ji Z, et al. Among authors: yates m. Bioorg Med Chem Lett. 2006 Aug 15;16(16):4326-30. doi: 10.1016/j.bmcl.2006.05.057. Epub 2006 Jun 2. Bioorg Med Chem Lett. 2006. PMID: 16735117

3

Lead optimization of methionine aminopeptidase-2 (MetAP2) inhibitors containing sulfonamides of 5,6-disubstituted anthranilic acids.

Wang GT, Mantei RA, Kawai M, Tedrow JS, Barnes DM, Wang J, Zhang Q, Lou P, Garcia LA, Bouska J, Yates M, Park C, Judge RA, Lesniewski R, Sheppard GS, Bell RL. Wang GT, et al. Among authors: yates m. Bioorg Med Chem Lett. 2007 May 15;17(10):2817-22. doi: 10.1016/j.bmcl.2007.02.062. Epub 2007 Feb 25. Bioorg Med Chem Lett. 2007. PMID: 17350258

4

N-terminal requirements of small peptide anticoagulants based on hirudin54-65.

Owen TJ, Krstenansky JL, Yates MT, Mao SJ. Owen TJ, et al. Among authors: yates mt. J Med Chem. 1988 May;31(5):1009-11. doi: 10.1021/jm00400a020. J Med Chem. 1988. PMID: 3361570

5

Antioxidant activity of probucol and its analogues in hypercholesterolemic Watanabe rabbits.

Mao SJ, Yates MT, Rechtin AE, Jackson RL, Van Sickle WA. Mao SJ, et al. Among authors: yates mt. J Med Chem. 1991 Jan;34(1):298-302. doi: 10.1021/jm00105a046. J Med Chem. 1991. PMID: 1992130

6

Positional effects of sulfation in hirudin and hirudin PA related anticoagulant peptides.

Payne MH, Krstenansky JL, Yates MT, Mao SJ. Payne MH, et al. Among authors: yates mt. J Med Chem. 1991 Mar;34(3):1184-7. doi: 10.1021/jm00107a043. J Med Chem. 1991. PMID: 2002458

7

Development of MDL 28,050, a small stable antithrombin agent based on a functional domain of the leech protein, hirudin.

Krstenansky JL, Broersma RJ, Owen TJ, Payne MH, Yates MT, Mao SJ. Krstenansky JL, et al. Among authors: yates mt. Thromb Haemost. 1990 Apr 12;63(2):208-14. Thromb Haemost. 1990. PMID: 2363122

8

The C-terminal binding domain of hirullin P18. Antithrombin activity and comparison to hirudin peptides.

Krstenansky JL, Owen TJ, Yates MT, Mao SJ. Krstenansky JL, et al. Among authors: yates mt. FEBS Lett. 1990 Sep 3;269(2):425-9. doi: 10.1016/0014-5793(90)81208-6. FEBS Lett. 1990. PMID: 2401369 Free article.

9

Preparation of antibodies to a synthetic C terminus of hirudin and identification of an antigenic site.

Mao SJ, Yates MT, Owen TJ, Krstenansky JL. Mao SJ, et al. Among authors: yates mt. J Immunol Methods. 1989 Jun 2;120(1):45-50. doi: 10.1016/0022-1759(89)90287-1. J Immunol Methods. 1989. PMID: 2471745

10

C-terminal peptide alcohol, acid and amide analogs of desulfato hirudin54-65 as antithrombin agents.

Krstenansky JL, Payne MH, Owen TJ, Yates MT, Mao SJ. Krstenansky JL, et al. Among authors: yates mt. Thromb Res. 1989 May 15;54(4):319-25. doi: 10.1016/0049-3848(89)90090-x. Thromb Res. 1989. PMID: 2763270

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