Williams M - Search Results

1

Synthesis, opioid receptor binding profile, and antinociceptive activity of 1-azaspiro[4.5]decan-10-yl amides.

Fujimoto RA, Boxer J, Jackson RH, Simke JP, Neale RF, Snowhill EW, Barbaz BJ, Williams M, Sills MA. Fujimoto RA, et al. Among authors: williams m. J Med Chem. 1989 Jun;32(6):1259-65. doi: 10.1021/jm00126a019. J Med Chem. 1989. PMID: 2542556

2

2H-[1]benzopyrano[3,4-b]pyridines: synthesis and activity at central monoamine receptors.

Hutchison A, Williams M, de Jesus R, Stone GA, Sylvester L, Clarke FH, Sills MA. Hutchison A, et al. Among authors: williams m. J Med Chem. 1989 Mar;32(3):720-7. doi: 10.1021/jm00123a039. J Med Chem. 1989. PMID: 2537429

3

4-(Phosphonoalkyl)- and 4-(phosphonoalkenyl)-2-piperidinecarboxylic acids: synthesis, activity at N-methyl-D-aspartic acid receptors, and anticonvulsant activity.

Hutchison AJ, Williams M, Angst C, de Jesus R, Blanchard L, Jackson RH, Wilusz EJ, Murphy DE, Bernard PS, Schneider J, et al. Hutchison AJ, et al. Among authors: williams m. J Med Chem. 1989 Sep;32(9):2171-8. doi: 10.1021/jm00129a025. J Med Chem. 1989. PMID: 2549246

4

Benzofuro[2,3-c]pyridin-6-ols: synthesis, affinity for opioid-receptor subtypes, and antinociceptive activity.

Hutchison AJ, de Jesus R, Williams M, Simke JP, Neale RF, Jackson RH, Ambrose F, Barbaz BJ, Sills MA. Hutchison AJ, et al. Among authors: williams m. J Med Chem. 1989 Sep;32(9):2221-6. doi: 10.1021/jm00129a031. J Med Chem. 1989. PMID: 2549247

5

Characterization of quisqualate recognition sites in rat brain tissue using DL-[3H]alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA) and a filtration assay.

Murphy DE, Snowhill EW, Williams M. Murphy DE, et al. Among authors: williams m. Neurochem Res. 1987 Sep;12(9):775-81. doi: 10.1007/BF00971514. Neurochem Res. 1987. PMID: 2890112

6

Characterization of the binding of a novel nonxanthine adenosine antagonist radioligand, [3H]CGS 15943, to multiple affinity states of the adenosine A1 receptor in the rat cortex.

Jarvis MF, Williams M, Do UH, Sills MA. Jarvis MF, et al. Among authors: williams m. Mol Pharmacol. 1991 Jan;39(1):49-54. Mol Pharmacol. 1991. PMID: 1987452

7

[3H]CGS 21680, a selective A2 adenosine receptor agonist directly labels A2 receptors in rat brain.

Jarvis MF, Schulz R, Hutchison AJ, Do UH, Sills MA, Williams M. Jarvis MF, et al. Among authors: williams m. J Pharmacol Exp Ther. 1989 Dec;251(3):888-93. J Pharmacol Exp Ther. 1989. PMID: 2600819

8

Autoradiographic characterization of high-affinity adenosine A2 receptors in the rat brain.

Jarvis MF, Jackson RH, Williams M. Jarvis MF, et al. Among authors: williams m. Brain Res. 1989 Apr 10;484(1-2):111-8. doi: 10.1016/0006-8993(89)90353-3. Brain Res. 1989. PMID: 2713675

9

Characterization of the binding of [3H]-CGS 19755: a novel N-methyl-D-aspartate antagonist with nanomolar affinity in rat brain.

Murphy DE, Hutchison AJ, Hurt SD, Williams M, Sills MA. Murphy DE, et al. Among authors: williams m. Br J Pharmacol. 1988 Nov;95(3):932-8. doi: 10.1111/j.1476-5381.1988.tb11723.x. Br J Pharmacol. 1988. PMID: 2850065 Free PMC article.

10

The NMDA antagonists, CPP and CGS 19755, lack affinity for central benzodiazepine receptors.

Williams M, Loo PS, Sills MA. Williams M, et al. Eur J Pharmacol. 1988 Oct 11;155(1-2):185-7. doi: 10.1016/0014-2999(88)90421-9. Eur J Pharmacol. 1988. PMID: 2854072

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