Lodge D - Search Results

1

(3SR,4aRS,6SR,8aRS)-6-(1H-tetrazol-5-yl)decahydroisoquinoline-3-carboxylic acid, a novel, competitive, systemically active NMDA and AMPA receptor antagonist.

Ornstein PL, Arnold MB, Allen NK, Leander JD, Tizzano JP, Lodge D, Schoepp DD. Ornstein PL, et al. Among authors: lodge d. J Med Chem. 1995 Dec 8;38(25):4885-90. doi: 10.1021/jm00025a005. J Med Chem. 1995. PMID: 8523401

2

Heteroatom-substitution as a strategy for increasing the potency of competitive NMDA antagonists.

Ornstein PL, Arnold MB, Lunn WH, Heinz LJ, Leander JD, Lodge D, Schoepp DD. Ornstein PL, et al. Among authors: lodge d. Bioorg Med Chem Lett. 1998 Feb 17;8(4):389-94. doi: 10.1016/s0960-894x(98)00038-9. Bioorg Med Chem Lett. 1998. PMID: 9871691

3

Synthesis and anticonvulsant activity of 3-aryl-5H-2,3-benzodiazephine AMPA antagonists.

Anderson BA, Harn NK, Hansen MM, Harkness AR, Lodge D, Leander JD. Anderson BA, et al. Among authors: lodge d. Bioorg Med Chem Lett. 1999 Jul 19;9(14):1953-6. doi: 10.1016/s0960-894x(99)00315-7. Bioorg Med Chem Lett. 1999. PMID: 10450961

4

Synthesis and excitatory amino acid pharmacology of a series of heterocyclic-fused quinoxalinones and quinazolinones.

McQuaid LA, Smith EC, South KK, Mitch CH, Schoepp DD, True RA, Calligaro DO, O'Malley PJ, Lodge D, Ornstein PL. McQuaid LA, et al. Among authors: lodge d. J Med Chem. 1992 Sep 4;35(18):3319-24. doi: 10.1021/jm00096a002. J Med Chem. 1992. PMID: 1382133

5

NMDA antagonist activity of (+/-)-(2SR,4RS)-4-(1H-tetrazol-5-ylmethyl)piperidine-2-carboxylic acid resides with the (-)-2R,4S-isomer.

Ornstein PL, Schoepp DD, Arnold MB, Jones ND, Deeter JB, Lodge D, Leander JD. Ornstein PL, et al. Among authors: lodge d. J Med Chem. 1992 Aug 21;35(17):3111-5. doi: 10.1021/jm00095a004. J Med Chem. 1992. PMID: 1387167

6

6-substituted decahydroisoquinoline-3-carboxylic acids as potent and selective conformationally constrained NMDA receptor antagonists.

Ornstein PL, Schoepp DD, Arnold MB, Augenstein NK, Lodge D, Millar JD, Chambers J, Campbell J, Paschal JW, Zimmerman DM, et al. Ornstein PL, et al. Among authors: lodge d. J Med Chem. 1992 Sep 18;35(19):3547-60. doi: 10.1021/jm00097a012. J Med Chem. 1992. PMID: 1404235

7

D,L-(tetrazol-5-yl) glycine: a novel and highly potent NMDA receptor agonist.

Schoepp DD, Smith CL, Lodge D, Millar JD, Leander JD, Sacaan AI, Lunn WH. Schoepp DD, et al. Among authors: lodge d. Eur J Pharmacol. 1991 Oct 15;203(2):237-43. doi: 10.1016/0014-2999(91)90719-7. Eur J Pharmacol. 1991. PMID: 1686860

8

4-(Tetrazolylalkyl)piperidine-2-carboxylic acids. Potent and selective N-methyl-D-aspartic acid receptor antagonists with a short duration of action.

Ornstein PL, Schoepp DD, Arnold MB, Leander JD, Lodge D, Paschal JW, Elzey T. Ornstein PL, et al. Among authors: lodge d. J Med Chem. 1991 Jan;34(1):90-7. doi: 10.1021/jm00105a016. J Med Chem. 1991. PMID: 1825117

9

Pharmacological characterization of LY233053: a structurally novel tetrazole-substituted competitive N-methyl-D-aspartic acid antagonist with a short duration of action.

Schoepp DD, Ornstein PL, Leander JD, Lodge D, Salhoff CR, Zeman S, Zimmerman DM. Schoepp DD, et al. Among authors: lodge d. J Pharmacol Exp Ther. 1990 Dec;255(3):1301-8. J Pharmacol Exp Ther. 1990. PMID: 2148188

10

LY233053: a structurally novel, potent and selective competitive N-methyl-D-aspartate receptor antagonist.

Ornstein PL, Schoepp DD, Leander JD, Wong T, Zimmerman DM, Lodge D. Ornstein PL, et al. Among authors: lodge d. Prog Clin Biol Res. 1990;361:429-33. Prog Clin Biol Res. 1990. PMID: 2149764 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

421 results

Search Page

Filters