Britcher SF - Search Results

1

L-743, 726 (DMP-266): a novel, highly potent nonnucleoside inhibitor of the human immunodeficiency virus type 1 reverse transcriptase.

Young SD, Britcher SF, Tran LO, Payne LS, Lumma WC, Lyle TA, Huff JR, Anderson PS, Olsen DB, Carroll SS, et al. Young SD, et al. Among authors: britcher sf. Antimicrob Agents Chemother. 1995 Dec;39(12):2602-5. doi: 10.1128/AAC.39.12.2602. Antimicrob Agents Chemother. 1995. PMID: 8592986 Free PMC article.

2

Synthesis of a series of 4-(arylethynyl)-6-chloro-4-cyclopropyl-3,4-dihydroquinazolin-2(1H)-ones as novel non-nucleoside HIV-1 reverse transcriptase inhibitors.

Tucker TJ, Lyle TA, Wiscount CM, Britcher SF, Young SD, Sanders WM, Lumma WC, Goldman ME, O'Brien JA, Ball RG, et al. Tucker TJ, et al. Among authors: britcher sf. J Med Chem. 1994 Jul 22;37(15):2437-44. doi: 10.1021/jm00041a023. J Med Chem. 1994. PMID: 7520079

3

HIV-1 protease inhibitors based on hydroxyethylene dipeptide isosteres: an investigation into the role of the P1' side chain on structure-activity.

Young SD, Payne LS, Thompson WJ, Gaffin N, Lyle TA, Britcher SF, Graham SL, Schultz TH, Deana AA, Darke PL, et al. Young SD, et al. Among authors: britcher sf. J Med Chem. 1992 May 15;35(10):1702-9. doi: 10.1021/jm00088a004. J Med Chem. 1992. PMID: 1588552

4

Synthesis and pharmacological evaluation of a series of dibenzo[a,d]cycloalkenimines as N-methyl-D-aspartate antagonists.

Thompson WJ, Anderson PS, Britcher SF, Lyle TA, Thies JE, Magill CA, Varga SL, Schwering JE, Lyle PA, Christy ME, et al. Thompson WJ, et al. Among authors: britcher sf. J Med Chem. 1990 Feb;33(2):789-808. doi: 10.1021/jm00164a052. J Med Chem. 1990. PMID: 1688947

5

Structure and activity of hydrogenated derivatives of (+)-5-methyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imine (MK-801).

Lyle TA, Magill CA, Britcher SF, Denny GH, Thompson WJ, Murphy JS, Knight AR, Kemp JA, Marshall GR, Middlemiss DN, et al. Lyle TA, et al. Among authors: britcher sf. J Med Chem. 1990 Mar;33(3):1047-52. doi: 10.1021/jm00165a026. J Med Chem. 1990. PMID: 2155319

6

Inhibitors of gastric acid secretion: 3,4-diamino-1,2,5-thiadiazole 1-oxides and 1,1-dioxides as urea equivalents in a series of histamine H2-receptor antagonists.

Lumma WC Jr, Anderson PS, Baldwin JJ, Bolhofer WA, Habecker CN, Hirshfield JM, Pietruszkiewicz AM, Randall WC, Torchiana ML, Britcher SF, Clineschmidt BV, Denny GH, Hirschmann R, Hoffman MJ, Phillips BT, Streeter KB. Lumma WC Jr, et al. Among authors: britcher sf. J Med Chem. 1982 Mar;25(3):207-10. doi: 10.1021/jm00345a002. J Med Chem. 1982. PMID: 6121913 No abstract available.

7

Synthesis and orexigenic activity of some 1-methyl-4-piperidylidene-Substituted pyrrolo[2,1-g][3] benzazepine and dibenzocycloheptene derivatives.

Remy DC, Britcher SF, Anderson PS, Bélanger PC, Girard Y, Clineschmidt BV. Remy DC, et al. Among authors: britcher sf. J Med Chem. 1982 Mar;25(3):231-4. doi: 10.1021/jm00345a008. J Med Chem. 1982. PMID: 7069703

8

Synthesis and receptor binding studies relevant to the neuroleptic activities of some 1-methyl-4-piperidylidene-9-substituted-pyrrolo[2,1-b][3]benzazepine derivatives.

Remy DC, Britcher SF, King SW, Anderson PS, Hunt CA, Randall WC, Bélanger P, Atkinson JG, Girard Y, Rooney CS, Fuentes JJ, Totaro JA, Robinson JL, Risley EA, Williams M. Remy DC, et al. Among authors: britcher sf. J Med Chem. 1983 Jul;26(7):974-80. doi: 10.1021/jm00361a008. J Med Chem. 1983. PMID: 6134835

9

Bridged bicyclic and polycyclic amino acids. Potent new inhibitors of the fibrinolytic process.

Loeffler LJ, Britcher SF, Baumgarten W. Loeffler LJ, et al. Among authors: britcher sf. J Med Chem. 1970 Sep;13(5):926-35. doi: 10.1021/jm00299a030. J Med Chem. 1970. PMID: 5458384 No abstract available.

10

Tyrosine hydroxylase inhibitors. Synthesis and activity of substituted aromatic amino acids.

Saari WS, Williams J, Britcher SF, Wolf DE, Kuehl FA Jr. Saari WS, et al. Among authors: britcher sf. J Med Chem. 1967 Nov;10(6):1008-14. doi: 10.1021/jm00318a005. J Med Chem. 1967. PMID: 6056025 No abstract available.

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