Literature DB >> 8273577

Pharmacological characterization of WAY-121,520: a potent anti-inflammatory indomethacin-based inhibitor of 5-lipoxygenase (5-LO)/phospholipase A2 (PLA2).

K B Glaser1, R P Carlson, A Sung, J Bauer, Y W Lock, D Holloway, R Sturm, D Hartman, T Walter, S Woeppel.   

Abstract

WAY-121,520 inhibited human synovial fluid PLA2 (HSF-PLA2) (IC50 = 4 microM) using arachidonic acid-labeled E. coli as substrate. Further biochemical characterization of WAY-121,520 demonstrated potent inhibition of 5-lipoxygenase (5-LO) activity in the murine macrophage (LTC4, IC50 = 4 nM) and rat PMN (LTB4, IC50 = 10 nM) and an ability to antagonize LTD4 binding to isolated guinea-pig trachea (pKB = 6.0). In vivo anti-inflammatory activity was noted in murine TPA-induced (ED50 = 91 micrograms/ear) and arachidonic acid-induced (66% inhibition at 400 micrograms/ear) ear edema and in leukotriene-dependent antigen-induced bronchoconstriction in the guinea pig (73% inhibition at 50 mg/kg, p.o.). WAY-121,520 represents a novel series of indomethacin-based inhibitors of PLA2 with anti-inflammatory activity resulting from a combination of biochemical activities (inhibition of 5-LO and PLA2 and LTD4 antagonism). This agent may provide added therapeutic efficacy over more selective inhibitors.

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Year:  1993        PMID: 8273577     DOI: 10.1007/bf01972711

Source DB:  PubMed          Journal:  Agents Actions        ISSN: 0065-4299


  8 in total

1.  Evaluation of antirheumatic drugs for their effect in vitro on purified human synovial fluid phospholipase A2.

Authors:  L A Marshall; J Bauer; M L Sung; J Y Chang
Journal:  J Rheumatol       Date:  1991-01       Impact factor: 4.666

2.  PAF and LTB4 biosynthesis in the human neutrophil: effects of putative inhibitors of phospholipase A2 and specific inhibitors of 5-lipoxygenase.

Authors:  K B Glaser; Y W Lock; J Y Chang
Journal:  Agents Actions       Date:  1991-09

3.  Low concentrations of indomethacin inhibit phospholipase A2 of rabbit polymorphonuclear leukocytes.

Authors:  L Kaplan; J Weiss; P Elsbach
Journal:  Proc Natl Acad Sci U S A       Date:  1978-06       Impact factor: 11.205

4.  Manoalide: structure-activity studies and definition of the pharmacophore for phospholipase A2 inactivation.

Authors:  K B Glaser; M S de Carvalho; R S Jacobs; M R Kernan; D J Faulkner
Journal:  Mol Pharmacol       Date:  1989-11       Impact factor: 4.436

5.  Some quantitative uses of drug antagonists.

Authors:  O ARUNLAKSHANA; H O SCHILD
Journal:  Br J Pharmacol Chemother       Date:  1959-03

6.  Structure-activity relationships leading to WAY-121,520, a tris aryl-type, indomethacin-based, phospholipase A2 (PLA2)/leukotriene biosynthesis inhibitor.

Authors:  A Kreft; J Nelson; J Musser; A Failli; U Shah; D Kubrak; A Banker; R Steffan; G Schiehser; R Sturm
Journal:  Agents Actions       Date:  1993

7.  Regulation of eicosanoid biosynthesis in vitro and in vivo by the marine natural product manoalide: a potent inactivator of venom phospholipases.

Authors:  A M Mayer; K B Glaser; R S Jacobs
Journal:  J Pharmacol Exp Ther       Date:  1988-03       Impact factor: 4.030

8.  Conversion of a cyclooxygenase (CO) inhibitor into a 5-lipoxygenase (LO) inhibitor: a general route to novel orally active anti-inflammatory and anti-allergy drugs.

Authors:  A F Kreft; A A Failli; J H Musser; D M Kubrak; A L Banker; R Steffan; C A Demerson; J A Nelson; U S Shah; W Gray
Journal:  Drugs Exp Clin Res       Date:  1991
  8 in total
  1 in total

1.  Computational drug repositioning for peripheral arterial disease: prediction of anti-inflammatory and pro-angiogenic therapeutics.

Authors:  Liang-Hui Chu; Brian H Annex; Aleksander S Popel
Journal:  Front Pharmacol       Date:  2015-08-25       Impact factor: 5.810

  1 in total

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