Brittelli DR - Search Results

1

An automated pulse labelling method for structure-activity relationship studies with antibacterial oxazolidinones.

Eustice DC, Brittelli DR, Feldman PA, Brown LJ, Borkowski JJ, Slee AM. Eustice DC, et al. Among authors: brittelli dr. Drugs Exp Clin Res. 1990;16(4):149-55. Drugs Exp Clin Res. 1990. PMID: 2127566

2

Antibacterials. Synthesis and structure-activity studies of 3-aryl-2-oxooxazolidines. 1. The "B" group.

Gregory WA, Brittelli DR, Wang CL, Wuonola MA, McRipley RJ, Eustice DC, Eberly VS, Bartholomew PT, Slee AM, Forbes M. Gregory WA, et al. Among authors: brittelli dr. J Med Chem. 1989 Aug;32(8):1673-81. doi: 10.1021/jm00128a003. J Med Chem. 1989. PMID: 2502627

3

Antibacterials. synthesis and structure-activity studies of 3-aryl-2-oxooxazolidines. 4. Multiply-substituted aryl derivatives.

Park CH, Brittelli DR, Wang CL, Marsh FD, Gregory WA, Wuonola MA, McRipley RJ, Eberly VS, Slee AM, Forbes M. Park CH, et al. Among authors: brittelli dr. J Med Chem. 1992 Mar 20;35(6):1156-65. doi: 10.1021/jm00084a022. J Med Chem. 1992. PMID: 1552508

4

Antibacterials. Synthesis and structure-activity studies of 3-aryl-2-oxooxazolidines. 2. The "A" group.

Gregory WA, Brittelli DR, Wang CL, Kezar HS 3rd, Carlson RK, Park CH, Corless PF, Miller SJ, Rajagopalan P, Wuonola MA, et al. Gregory WA, et al. Among authors: brittelli dr. J Med Chem. 1990 Sep;33(9):2569-78. doi: 10.1021/jm00171a035. J Med Chem. 1990. PMID: 2118186

5

Imidazo[1,2-a]pyrazine diaryl ureas: inhibitors of the receptor tyrosine kinase EphB4.

Mitchell SA, Danca MD, Blomgren PA, Darrow JW, Currie KS, Kropf JE, Lee SH, Gallion SL, Xiong JM, Pippin DA, DeSimone RW, Brittelli DR, Eustice DC, Bourret A, Hill-Drzewi M, Maciejewski PM, Elkin LL. Mitchell SA, et al. Among authors: brittelli dr. Bioorg Med Chem Lett. 2009 Dec 15;19(24):6991-5. doi: 10.1016/j.bmcl.2009.10.037. Epub 2009 Oct 15. Bioorg Med Chem Lett. 2009. PMID: 19879134

6

Omega-carboxypyridyl substituted ureas as Raf kinase inhibitors: SAR of the amide substituent.

Khire UR, Bankston D, Barbosa J, Brittelli DR, Caringal Y, Carlson R, Dumas J, Gane T, Heald SL, Hibner B, Johnson JS, Katz ME, Kennure N, Kingery-Wood J, Lee W, Liu XG, Lowinger TB, McAlexander I, Monahan MK, Natero R, Renick J, Riedl B, Rong H, Sibley RN, Smith RA, Wolanin D. Khire UR, et al. Among authors: brittelli dr. Bioorg Med Chem Lett. 2004 Feb 9;14(3):783-6. doi: 10.1016/j.bmcl.2003.11.041. Bioorg Med Chem Lett. 2004. PMID: 14741289

7

Synthesis and structure activity relationships of novel small molecule cathepsin D inhibitors.

Dumas J, Brittelli D, Chen J, Dixon B, Hatoum-Mokdad H, König G, Sibley R, Witowsky J, Wong S. Dumas J, et al. Bioorg Med Chem Lett. 1999 Sep 6;9(17):2531-6. doi: 10.1016/s0960-894x(99)00433-3. Bioorg Med Chem Lett. 1999. PMID: 10498202

8

An approach to the design of novel cognitive enhancers using molecular modeling and X-ray crystallography.

Nugiel DA, Voss ME, Brittelli DR, Calabrese JC. Nugiel DA, et al. Among authors: brittelli dr. Drug Des Discov. 1995 Apr;12(4):289-95. Drug Des Discov. 1995. PMID: 9040989

9

Simple selection criteria for drug-like chemical matter.

Muegge I, Heald SL, Brittelli D. Muegge I, et al. J Med Chem. 2001 Jun 7;44(12):1841-6. doi: 10.1021/jm015507e. J Med Chem. 2001. PMID: 11384230

10

1,2-dibromopyracylene: a new aromatic system.

Trost BM, Brittelli DR. Trost BM, et al. Among authors: brittelli dr. Tetrahedron Lett. 1967 Jan;2:119-22. doi: 10.1016/s0040-4039(00)90498-2. Tetrahedron Lett. 1967. PMID: 4167203 No abstract available.

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