Peppard J - Search Results

1

Inhibition of LTB4 biosynthesis in situ by CGS 23885, a potent 5-lipoxygenase inhibitor, correlates with its pleural fluid concentrations in an experimentally induced rat pleurisy model.

Raychaudhuri A, Chertock H, Chovan J, Jones LS, Kimble EF, Kowalski TJ, Peppard J, White DH, Satoh Y, Roland D. Raychaudhuri A, et al. Among authors: peppard j. Naunyn Schmiedebergs Arch Pharmacol. 1997 Apr;355(4):470-4. doi: 10.1007/pl00004971. Naunyn Schmiedebergs Arch Pharmacol. 1997. PMID: 9109363

2

Effect of 5-lipoxygenase inhibitors on in situ LTB4 biosynthesis following calcium ionophore stimulation in the rat pleural cavity.

Raychaudhuri A, Chertock H, Peppard J, White WD, Koeler J, DiPasquale G. Raychaudhuri A, et al. Among authors: peppard j. Agents Actions. 1993;39 Spec No:C43-5. doi: 10.1007/BF01972715. Agents Actions. 1993. PMID: 8273581

3

Development of tolerance to the antihypertensive effects of highly selective adenosine A2a agonists upon chronic administration.

Webb RL, Sills MA, Chovan JP, Peppard JV, Francis JE. Webb RL, et al. Among authors: peppard jv. J Pharmacol Exp Ther. 1993 Oct;267(1):287-95. J Pharmacol Exp Ther. 1993. PMID: 8229754

4

Preclinical pharmacology of lumiracoxib: a novel selective inhibitor of cyclooxygenase-2.

Esser R, Berry C, Du Z, Dawson J, Fox A, Fujimoto RA, Haston W, Kimble EF, Koehler J, Peppard J, Quadros E, Quintavalla J, Toscano K, Urban L, van Duzer J, Zhang X, Zhou S, Marshall PJ. Esser R, et al. Among authors: peppard j. Br J Pharmacol. 2005 Feb;144(4):538-50. doi: 10.1038/sj.bjp.0706078. Br J Pharmacol. 2005. PMID: 15655513 Free PMC article.

5

Pharmacologic profile of CGS 24128, a potent, long-acting inhibitor of neutral endopeptidase 24.11.

Trapani AJ, Beil ME, Coté DT, de Lombaert S, Erion MD, Gerlock TE, Ghai RD, Hopkins MF, Peppard JV, Webb RL, et al. Trapani AJ, et al. Among authors: peppard jv. J Cardiovasc Pharmacol. 1994 Mar;23(3):358-64. J Cardiovasc Pharmacol. 1994. PMID: 7515977

6

The pharmacology of CGS 25462: a potent, orally bioavailable, long-acting inhibitor of neutral endopeptidase 24.11.

Trapani AJ, De Lombaert S, Erion MD, Ghai RD, Peppard JV, Lappe RW, Worcel M. Trapani AJ, et al. Among authors: peppard jv. J Hypertens Suppl. 1993 Dec;11(5):S220-1. J Hypertens Suppl. 1993. PMID: 8158354 No abstract available.

7

Inhibition of interleukin-1alpha-induced cartilage oligomeric matrix protein degradation in bovine articular cartilage by matrix metalloproteinase inhibitors: potential role for matrix metalloproteinases in the generation of cartilage oligomeric matrix protein fragments in arthritic synovial fluid.

Ganu V, Goldberg R, Peppard J, Rediske J, Melton R, Hu SI, Wang W, Duvander C, Heinegård D. Ganu V, et al. Among authors: peppard j. Arthritis Rheum. 1998 Dec;41(12):2143-51. doi: 10.1002/1529-0131(199812)41:12<2143::AID-ART9>3.0.CO;2-P. Arthritis Rheum. 1998. PMID: 9870871

8

Design and synthesis of an orally active macrocyclic neutral endopeptidase 24.11 inhibitor.

MacPherson LJ, Bayburt EK, Capparelli MP, Bohacek RS, Clarke FH, Ghai RD, Sakane Y, Berry CJ, Peppard JV, Trapani AJ. MacPherson LJ, et al. Among authors: peppard jv. J Med Chem. 1993 Nov 26;36(24):3821-8. doi: 10.1021/jm00076a009. J Med Chem. 1993. PMID: 8254611

9

Characterization of an interleukin 6 cytokine family antagonist protein from a marine sponge, Callyspongia sp.

Peppard JV, Loo P, Sills MA, Munster D, Pomponi SA, Wright AE. Peppard JV, et al. J Biol Chem. 1996 Mar 29;271(13):7281-4. doi: 10.1074/jbc.271.13.7281. J Biol Chem. 1996. PMID: 8631742 Free article.

10

Pharmacological modulation of rat monocytes: in vivo effects on Ia expression and interleukin-1 production.

Schenkelaars EJ, Singh HN, Goldberg RL, Doughty JR, Peppard J, DiPasquale G, Quagliata F. Schenkelaars EJ, et al. Among authors: peppard j. Agents Actions. 1991 Sep;34(1-2):66-9. doi: 10.1007/BF01993240. Agents Actions. 1991. PMID: 1793054

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