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5,870 results
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Beta-proline analogues as agonists at the strychnine-sensitive glycine receptor.
Johnson G, Drummond JT, Boxer PA, Bruns RF. Johnson G, et al. J Med Chem. 1992 Jan 24;35(2):233-41. doi: 10.1021/jm00080a006. J Med Chem. 1992. PMID: 1310117
Feasibility of an immunoassay for mevalonolactone.
Spencer TA, Clark DS, Johnson GA, Erickson SK, Curtiss LK. Spencer TA, et al. Among authors: johnson ga. Bioorg Med Chem. 1997 May;5(5):873-82. doi: 10.1016/s0968-0896(97)00032-1. Bioorg Med Chem. 1997. PMID: 9208099
Synthesis and pharmacological evaluation of 4a-phenanthrenamine derivatives acting at the phencyclidine binding site of the N-methyl-D-aspartate receptor complex.
Bigge CF, Malone TC, Hays SJ, Johnson G, Novak PM, Lescosky LJ, Retz DM, Ortwine DF, Probert AW Jr, Coughenour LL, et al. Bigge CF, et al. Among authors: johnson g. J Med Chem. 1993 Jul 9;36(14):1977-95. doi: 10.1021/jm00066a007. J Med Chem. 1993. PMID: 8336337
Synthesis and pharmacological evaluation of hexahydrofluorenamines as noncompetitive antagonists at the N-methyl-D-aspartate receptor.
Hays SJ, Novak PM, Ortwine DF, Bigge CF, Colbry NL, Johnson G, Lescosky LJ, Malone TC, Michael A, Reily MD, et al. Hays SJ, et al. Among authors: johnson g. J Med Chem. 1993 Mar 19;36(6):654-70. doi: 10.1021/jm00058a002. J Med Chem. 1993. PMID: 8459395
Substituted 2-benzothiazolamines as sodium flux inhibitors: quantitative structure-activity relationships and anticonvulsant activity.
Hays SJ, Rice MJ, Ortwine DF, Johnson G, Schwarz RD, Boyd DK, Copeland LF, Vartanian MG, Boxer PA. Hays SJ, et al. Among authors: johnson g. J Pharm Sci. 1994 Oct;83(10):1425-32. doi: 10.1002/jps.2600831013. J Pharm Sci. 1994. PMID: 7884664
Identification and evaluation of O-alkyl substituted hydroxamic acids as potent in vitro inhibitors of the hepatic glycine cleavage system and investigation of their action on in vivo central nervous system glycine concentration.
Johnson G, Boxer PA, Drummond JT, Boyd DK, Anderson RJ. Johnson G, et al. Arzneimittelforschung. 1989 Apr;39(4):432-7. Arzneimittelforschung. 1989. PMID: 2751729
Evaluation and synthesis of aminohydroxyisoxazoles and pyrazoles as potential glycine agonists.
Drummond J, Johnson G, Nickell DG, Ortwine DF, Bruns RF, Welbaum B. Drummond J, et al. Among authors: johnson g. J Med Chem. 1989 Sep;32(9):2116-28. doi: 10.1021/jm00129a016. J Med Chem. 1989. PMID: 2549245
Exploration of phenyl-spaced 2-amino-(5-9)-phosphonoalkanoic acids as competitive N-methyl-D-aspartic acid antagonists.
Bigge CF, Drummond JT, Johnson G, Malone T, Probert AW Jr, Marcoux FW, Coughenour LL, Brahce LJ. Bigge CF, et al. Among authors: johnson g. J Med Chem. 1989 Jul;32(7):1580-90. doi: 10.1021/jm00127a030. J Med Chem. 1989. PMID: 2544728
New and versatile approaches to the synthesis of CPP-related competitive NMDA antagonists. Preliminary structure-activity relationships and pharmacological evaluation.
Hays SJ, Bigge CF, Novak PM, Drummond JT, Bobovski TP, Rice MJ, Johnson G, Brahce LJ, Coughenour LL. Hays SJ, et al. Among authors: johnson g. J Med Chem. 1990 Oct;33(10):2916-24. doi: 10.1021/jm00172a037. J Med Chem. 1990. PMID: 2145436
Exploration of N-phosphonoalkyl-, N-phosphonoalkenyl-, and N-(phosphonoalkyl)phenyl-spaced alpha-amino acids as competitive N-methyl-D-aspartic acid antagonists.
Bigge CF, Johnson G, Ortwine DF, Drummond JT, Retz DM, Brahce LJ, Coughenour LL, Marcoux FW, Probert AW Jr. Bigge CF, et al. Among authors: johnson g. J Med Chem. 1992 Apr 17;35(8):1371-84. doi: 10.1021/jm00086a005. J Med Chem. 1992. PMID: 1533423
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