58 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Romazarit: a potential disease-modifying antirheumatic drug.

Roche Products
Synthesis and quantitative structure-activity relationships of diclofenac analogues.

Ciba-Geigy
Antiinflammatory activity of a series of substituted 2,3-dihydro-6-hydroxypyrimido[2,1-f]purine-4,8(1H,9H)-diones.

Schering-Plough
Antiinflammatory 2,6-di-tert-butyl-4-(2-arylethenyl)phenols.

Boehringer Ingelheim Pharmaceuticals
Benzimidazole derivatives with atypical antiinflammatory activity.

TBA
Synthesis and antiinflammatory/analgesic activities of 11H-dibenzo[b, e,][1,4]dioxepinacetic acids.

TBA
Antiinflammatory activity of substituted 6-hydroxypyrimido[2,1-f]purine-2,4,8(1H,3H,9H)-triones. Atypical nonsteroidal antiinflammatory agents.

TBA
Bulky amine analogues of ketoprofen: potent antiinflammatory agents.

TBA
Antiinflammatory agents. 3. Synthesis and pharmacological evaluation of 2-amino-3-benzoylphenylacetic acid and analogues.

TBA
Antiinflammatory activity of N-(2-benzoylphenyl)alanine derivatives.

TBA
Antiinflammatory agents. 2. Syntheses and antiinflammatory activity of substituted 2-aminophenylacetic acid derivatives.

TBA
2,3-Dihydrobenzofuran-2-ones: a new class of highly potent antiinflammatory agents.

TBA
Synthesis and antiinflammatory activity of some 2-(substituted-pyridinyl)benzimidazoles.

TBA
Basic antiinflammatory compounds. N,N',N''-Trisubstituted guanidines.

TBA
Synthesis of unsymmetrical monocarbonyl curcumin analogues with potent inhibition on prostaglandin E2 production in LPS-induced murine and human macrophages cell lines.

Universiti Kebangsaan Malaysia
Indazolinones, a new series of redox-active 5-lipoxygenase inhibitors with built-in selectivity and oral activity.

Ici Pharmaceuticals Group
Designed multiple ligands. An emerging drug discovery paradigm.

Organon Laboratories
Novel 1,2,4-oxadiazoles and 1,2,4-thiadiazoles as dual 5-lipoxygenase and cyclooxygenase inhibitors.

Warner-Lambert
5-lipoxygenase: properties, pharmacology, and the quinolinyl(bridged)aryl class of inhibitors.

Wyeth-Ayerst Research
1,2-Dihydro-1-oxopyrrolo[3,2,1-kl]phenothiazine-2-carboxamides and congeners, dual cyclooxygenase/5-lipoxygenase inhibitors with antiinflammatory activity.

Pfizer
2-substituted-1-naphthols as potent 5-lipoxygenase inhibitors with topical antiinflammatory activity.

E.I. Du Pont De Nemours
4-Hydroxy-3-quinolinecarboxamides with antiarthritic and analgesic activities.

Centre De Recherches Roussel-Uclaf
Imidazo[1,5-a]pyridines: a new class of thromboxane A2 synthetase inhibitors.

TBA
Antiinflammatory -benzeneethanamines. III

TBA
Topical antiinflammatory dehydroabietylamine derivatives. IV

TBA
Cyclooxygenase and 5-lipoxygenase inhibitory activity of 2,6 di-
t-butylphenols linked by a sulfur atom to 1,3,4-thiadiazoles and 1,3,4-oxadiazoles

TBA
Vinylogous hydroxamic acids: 5-lipoxygenase inhibitors

TBA
Synthesis and cyclooxygenase and 5-lipoxygenase inhibitory activity of some thiazolidene-4-one analogs of meclofenamic acid

TBA
Synthesis of reversed hydroxamic acids of indomethacin: dual inhibitors of cyclooxygenase and 5-lipoxygenase

TBA
1-Phenyl-[2H]-tetrahydropyridazin-3-one, A-53612, a selective orally active 5-lipoxygenase inhibitor

TBA
Conversion of NSAIDS into balanced dual inhibitors of cyclooxygenase and 5-lipoxygenase

TBA
Distribution of Bibenzyls, Prenyl Bibenzyls, Bis-bibenzyls, and Terpenoids in the Liverwort Genus

Tokushima Bunri University
N-hydroxyurea and hydroxamic acid inhibitors of cyclooxygenase and 5-lipoxygenase.

The R. W. Johnson Pharmaceutical Research Institute
Multitargeted Imidazoles: Potential Therapeutic Leads for Alzheimer's and Other Neurodegenerative Diseases.

University of Pennsylvania
1,3,4-Oxadiazole, 1,3,4-thiadiazole, and 1,2,4-triazole analogs of the fenamates: in vitro inhibition of cyclooxygenase and 5-lipoxygenase activities.

Warner-Lambert
3,4-Dihydroxychalcones as potent 5-lipoxygenase and cyclooxygenase inhibitors.

Tokushima Bunri University
Substituted chromenes as potent, orally active 5-lipoxygenase inhibitors.

Ciba-Geigy
Novel antiarthritic agents with 1,2-isothiazolidine-1,1-dioxide (gamma-sultam) skeleton: cytokine suppressive dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase.

Shionogi
Design, synthesis, and biochemical evaluation of N-substituted maleimides as inhibitors of prostaglandin endoperoxide synthases.

Vanderbilt University School of Medicine
Selective thromboxane synthetase inhibitors. 1. 1-[(Aryloxy)alkyl]-1H-imidazoles.

TBA
Leukotriene D4 antagonists and 5-lipoxygenase inhibitors. Synthesis of benzoheterocyclic [(methoxyphenyl)amino]oxoalkanoic acid esters.

TBA
Phenylephrine derivatives as leukotriene D4 antagonists.

Wyeth Laboratories
Acetohydroxamic acids as potent, selective, orally active 5-lipoxygenase inhibitors.

Wellcome Research Laboratories
Selective thromboxane synthetase inhibitors. 4. 2-(1H-imidazol-1-ylmethyl) carboxylic acids of benzo[b]furan, benzo[b]thiophene, indole, and naphthalene.

TBA
Synthesis of [[(naphthalenylmethoxy)- and [[(quinolinylmethoxy)phenyl]amino]oxoalkanoic acid esters. A novel series of leukotriene D4 antagonists and 5-lipoxygenase inhibitors.

TBA
Selective thromboxane synthetase inhibitors. 2. 3-(1H-imidazol-1-ylmethyl)-2-methyl-1H-indole-1-propanoic acid and analogues.

TBA
Evaluation of Oxetan-3-ol, Thietan-3-ol, and Derivatives Thereof as Bioisosteres of the Carboxylic Acid Functional Group.

University of Pennsylvania
Differential effects of a series of hydroxamic acid derivatives on 5-lipoxygenase and cyclooxygenase from neutrophils and 12-lipoxygenase from platelets and their in vivo effects on inflammation and anaphylaxis.

Rorer Central Research
N-[(arylmethoxy)phenyl] and N-[(arylmethoxy)naphthyl] sulfonamides: potent orally active leukotriene D4 antagonists of novel structure.

Wyeth-Ayerst Research
Discovery of new indomethacin-based analogs with potentially selective cyclooxygenase-2 inhibition and observed diminishing to PGE2 activities.

Damanhour University
Penta- and hexadienoic acid derivatives: a novel series of 5-lipoxygenase inhibitors.

Centre De Recherches De Vitry
Antiinflammatory agents. 4. Syntheses and biological evaluation of potential prodrugs of 2-amino-3-benzoylbenzeneacetic acid and 2-amino-3-(4-chlorobenzoyl)benzeneacetic acid.

A.H. Robins
Nonsteroidal antiinflammatory drug hydroxamic acids. Dual inhibitors of both cyclooxygenase and 5-lipoxygenase.

Warner-Lambert
Effect of structure on potency and selectivity in 2,6-disubstituted 4-(2-arylethenyl)phenol lipoxygenase inhibitors.

Boehringer Ingelheim Pharmaceuticals
N-[(arylmethoxy)phenyl] carboxylic acids, hydroxamic acids, tetrazoles, and sulfonyl carboxamides. Potent orally active leukotriene D4 antagonists of novel structure.

Wyeth-Ayerst Research
Styrylpyrazoles, styrylisoxazoles, and styrylisothiazoles. Novel 5-lipoxygenase and cyclooxygenase inhibitors.

Warner-Lambert
Novel 1-(pyridylphenyl)-1-phenyl-2-imidazolylethanols with topical antiinflammatory activity.

Dupont Pharmaceuticals