The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
26638042 |
5 |
Discovery of novel hybrids of diaryl-1,2,4-triazoles and caffeic acid as dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase for cancer therapy. |
China Pharmaceutical University |
25462262 |
98 |
Development and evaluation of ST-1829 based on 5-benzylidene-2-phenylthiazolones as promising agent for anti-leukotriene therapy. |
Goethe-University Frankfurt |
1848292 |
116 |
Indazolinones, a new series of redox-active 5-lipoxygenase inhibitors with built-in selectivity and oral activity. |
Ici Pharmaceuticals Group |
| 4 |
Cyclic aryl hydroxamic acids: synthesis and inhibition of 5-lipoxygenase |
TBA |
22380511 |
73 |
Dynamic modeling of human 5-lipoxygenase-inhibitor interactions helps to discover novel inhibitors. |
Peking University |
9207936 |
198 |
Structure-activity relationships of N-hydroxyurea 5-lipoxygenase inhibitors. |
Abbott Laboratories |
8831759 |
16 |
1-substituted 4-aryl-5-pyridinylimidazoles: a new class of cytokine suppressive drugs with low 5-lipoxygenase and cyclooxygenase inhibitory potency. |
Smithkline Beecham Pharmaceuticals |
7932529 |
37 |
Novel dual inhibitors of 5-lipoxygenase and thromboxane A2 synthetase: synthesis and structure-activity relationships of 3-pyridylmethyl-substituted 2-amino-6-hydroxybenzothiazole derivatives. |
Eisai |
8478906 |
25 |
Design of 5-(3,5-di-tert-butyl-4-hydroxyphenyl)-1,3,4-thiadiazoles, -1,3,4-oxadiazoles, and -1,2,4-triazoles as orally-active, nonulcerogenic antiinflammatory agents. |
Warner-Lambert |
1433181 |
39 |
Novel 1,2,4-oxadiazoles and 1,2,4-thiadiazoles as dual 5-lipoxygenase and cyclooxygenase inhibitors. |
Warner-Lambert |
1635053 |
47 |
5-lipoxygenase: properties, pharmacology, and the quinolinyl(bridged)aryl class of inhibitors. |
Wyeth-Ayerst Research |
2113951 |
134 |
1,2-Dihydro-1-oxopyrrolo[3,2,1-kl]phenothiazine-2-carboxamides and congeners, dual cyclooxygenase/5-lipoxygenase inhibitors with antiinflammatory activity. |
Pfizer |
2104936 |
98 |
2-substituted-1-naphthols as potent 5-lipoxygenase inhibitors with topical antiinflammatory activity. |
E.I. Du Pont De Nemours |
3133478 |
16 |
4-Hydroxy-3-quinolinecarboxamides with antiarthritic and analgesic activities. |
Centre De Recherches Roussel-Uclaf |
3599023 |
29 |
Synthesis and 5-lipoxygenase inhibitory activity of 5-hydroperoxy-6,8,11,14-eicosatetraenoic acid analogues. |
TBA |
3820229 |
51 |
Hydroxamic acid inhibitors of 5-lipoxygenase. |
TBA |
3806609 |
30 |
Structural requirements for the inhibition of 5-lipoxygenase by 15-hydroxyeicosa-5,8,11,13-tetraenoic acid analogues. |
TBA |
3681891 |
27 |
Novel 1H-benzimidazol-4-ols with potent 5-lipoxygenase inhibitory activity. |
Beecham Pharmaceuticals Research Division |
| 35 |
Antiinflammatory -benzeneethanamines. III |
TBA |
| 22 |
Topical antiinflammatory dehydroabietylamine derivatives. IV |
TBA |
| 39 |
O-alkylcarboxylate oxime and N-hydroxyurea analogs of substituted indole leukotriene biosynthesis inhibitors |
TBA |
| 19 |
Catechol based inhibitors of 15-lipoxygenase |
TBA |
| 42 |
Cmi-206: A potent dual platelet activating factor antagonist and 5-lipoxygenase inhibitor |
TBA |
| 8 |
Synthesis and pharmacological profile of two novel heterocyclic chromanols, CP-80,798 and CP-85,958, as potent LTD4 receptor antagonists |
TBA |
| 76 |
2,4,5- triarylimidazole inhibitors of IL-1 biosynthesis |
TBA |
| 14 |
A novel series of highly potent 5-lipoxygenase inhibitors; 2-aryldienylbenzoxazoles |
TBA |
| 13 |
Design of pyrrolo-1,4-benzoxazine derivatives as inhibitors of 5-lipoxygenase and PAF antagonists with anthihistaminic properties |
TBA |
| 12 |
4-[5-(2,3-dihydroxyphenyl)pentyloxy]-2-hydroxy-3-propylbenzoic acid (Ro 24-0553): an orally active 5-lipoxygenase inhibitor with antiinflammatory activity |
TBA |
| 11 |
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 |
| 24 |
Vinylogous hydroxamic acids: 5-lipoxygenase inhibitors |
TBA |
| 11 |
Synthesis and cyclooxygenase and 5-lipoxygenase inhibitory activity of some thiazolidene-4-one analogs of meclofenamic acid |
TBA |
| 17 |
Development of L-689,065 - the prototype of a new class of potent 5-lipoxygenase inhibitors |
TBA |
| 16 |
Synthesis of reversed hydroxamic acids of indomethacin: dual inhibitors of cyclooxygenase and 5-lipoxygenase |
TBA |
| 21 |
1-Phenyl-[2H]-tetrahydropyridazin-3-one, A-53612, a selective orally active 5-lipoxygenase inhibitor |
TBA |
| 19 |
Structural analysis of 2-aryl-1,3-dione compounds as inhibitors of 5-lipoxygenase |
TBA |
| 14 |
Conversion of NSAIDS into balanced dual inhibitors of cyclooxygenase and 5-lipoxygenase |
TBA |
10514305 |
4 |
Novel and known constituents from Buddleja species and their activity against leukocyte eicosanoid generation. |
Peking Union Medical College And Chinese Academy Of Medical Sciences |
17336065 |
12 |
Indole derivatives as potent inhibitors of 5-lipoxygenase: design, synthesis, biological evaluation, and molecular modeling. |
Chinese Academy Of Sciences |
15081022 |
20 |
5-lipoxygenase inhibitors with histamine H(1) receptor antagonist activity. |
Ucb Pharma |
11277534 |
3 |
N-Aminoindoline derivatives as inhibitors of 5-lipoxygenase. |
Université |
10230624 |
110 |
N-hydroxyurea and hydroxamic acid inhibitors of cyclooxygenase and 5-lipoxygenase. |
The R. W. Johnson Pharmaceutical Research Institute |
9599246 |
28 |
(+/-)-trans-2-[3-methoxy-4-(4-chlorophenylthioethoxy)-5-(N-methyl-N- hydroxyureidyl)methylphenyl]-5-(3,4, 5-trimethoxyphenyl)tetrahydrofuran (CMI-392), a potent dual 5-lipoxygenase inhibitor and platelet-activating factor receptor antagonist. |
University Of Virginia |
9544212 |
37 |
New cyclooxygenase-2/5-lipoxygenase inhibitors. 2. 7-tert-butyl-2,3-dihydro-3,3-dimethylbenzofuran derivatives as gastrointestinal safe antiinflammatory and analgesic agents: variations of the dihydrobenzofuran ring. |
Procter & Gamble Pharmaceuticals |
9484493 |
11 |
Design, synthesis, and biological evaluation of conformationally constrained aci-reductone mimics of arachidonic acid. |
Oxis International |
9057869 |
25 |
Nonsteroidal anti-inflammatory drugs as scaffolds for the design of 5-lipoxygenase inhibitors. |
Abbott Laboratories |
8978834 |
33 |
Bicyclic N-hydroxyurea inhibitors of 5-lipoxygenase: pharmacodynamic, pharmacokinetic, and in vitro metabolic studies characterizing N-hydroxy-N-(2,3-dihydro-6-(phenylmethoxy)-3-benzofuranyl)urea. |
Smithkline Beecham Pharmaceuticals |
8831760 |
108 |
5-Lipoxygenase inhibitors: synthesis and structure-activity relationships of a series of 1-aryl-2H,4H-tetrahydro-1,2,4-triazin-3-ones. |
Abbott Laboratories |
8809171 |
13 |
(E)-3-[6-[[(2,6-dichlorophenyl)thio]methyl]-3-(2-phenylethoxy)-2- pyridinyl]-2-propenoic acid: a high-affinity leukotriene B4 receptor antagonist with oral antiinflammatory activity. |
Smithkline Beecham Pharmaceuticals |
8568814 |
23 |
Dibenzoxepinone hydroxylamines and hydroxamic acids: dual inhibitors of cyclooxygenase and 5-lipoxygenase with potent topical antiinflammatory activity. |
Hoechst-Roussel Pharmaceuticals |
8515419 |
29 |
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 |
8410991 |
88 |
Substituted thiopyrano[2,3,4-c,d]indoles as potent, selective, and orally active inhibitors of 5-lipoxygenase. Synthesis and biological evaluation of L-691,816. |
Merck Frosst Centre For Therapeutic Research |
8295221 |
28 |
Synthesis and biological evaluation of 5-[[3,5-bis(1,1-dimethylethyl)- 4-hydroxyphenyl]methylene]oxazoles, -thiazoles, and -imidazoles: novel dual 5-lipoxygenase and cyclooxygenase inhibitors with antiinflammatory activity. |
Warner-Lambert |
8254620 |
62 |
3,4-Dihydroxychalcones as potent 5-lipoxygenase and cyclooxygenase inhibitors. |
Tokushima Bunri University |
8151626 |
4 |
Antiinflammatory 4,5-diarylpyrroles: synthesis and QSAR. |
Dupont Pharmaceuticals |
7932593 |
24 |
Synthesis and 5-lipoxygenase inhibitory activities of some novel 2-substituted 5-benzofuran hydroxamic acids. |
R. W. Johnson Pharmaceutical Research Institute |
7739006 |
2 |
Synthesis and antiinflammatory activity of certain 5,6,7,8-tetrahydroquinolines and related compounds. |
Wyeth Research (U.K.) |
3806620 |
16 |
Leukotriene D4 antagonists and 5-lipoxygenase inhibitors. Synthesis of benzoheterocyclic [(methoxyphenyl)amino]oxoalkanoic acid esters. |
TBA |
3783588 |
51 |
Syntheses of 5,6,7- and 5,7,8-trioxygenated 3',4'-dihydroxyflavones having alkoxy groups and their inhibitory activities against arachidonate 5-lipoxygenase. |
TBA |
3669019 |
11 |
In vivo characterization of hydroxamic acid inhibitors of 5-lipoxygenase. |
Abbott Laboratories |
3336029 |
8 |
Orally active hydroxamic acid inhibitors of leukotriene biosynthesis. |
Abbott Laboratories |
3172130 |
35 |
Structure-activity analysis of a class of orally active hydroxamic acid inhibitors of leukotriene biosynthesis. |
Abbott Laboratories |
3090264 |
28 |
Synthesis of [[(naphthalenylmethoxy)- and [[(quinolinylmethoxy)phenyl]amino]oxoalkanoic acid esters. A novel series of leukotriene D4 antagonists and 5-lipoxygenase inhibitors. |
TBA |
2878078 |
43 |
Synthesis and antiallergic activity of a novel series of 5-lipoxygenase inhibitors. |
TBA |
2542553 |
31 |
Synthesis and structure-activity relationships of a novel class of 5-lipoxygenase inhibitors. 2-(Phenylmethyl)-4-hydroxy-3,5-dialkylbenzofurans: the development of L-656,224. |
Merck Frosst Canada |
2502629 |
90 |
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 |
2498516 |
4 |
N-[(arylmethoxy)phenyl] and N-[(arylmethoxy)naphthyl] sulfonamides: potent orally active leukotriene D4 antagonists of novel structure. |
Wyeth-Ayerst Research |
2319562 |
12 |
Design, synthesis, and 5-lipoxygenase-inhibiting properties of 1-thio-substituted butadienes. |
Molecular Therapeutics |
2308149 |
221 |
Hydroxamic acid inhibitors of 5-lipoxygenase: quantitative structure-activity relationships. |
Abbott Laboratories |
2213827 |
73 |
Penta- and hexadienoic acid derivatives: a novel series of 5-lipoxygenase inhibitors. |
Centre De Recherches De Vitry |
2115586 |
29 |
Nonsteroidal antiinflammatory drug hydroxamic acids. Dual inhibitors of both cyclooxygenase and 5-lipoxygenase. |
Warner-Lambert |
2104935 |
10 |
N-[(arylmethoxy)phenyl] carboxylic acids, hydroxamic acids, tetrazoles, and sulfonyl carboxamides. Potent orally active leukotriene D4 antagonists of novel structure. |
Wyeth-Ayerst Research |
2066989 |
89 |
4-hydroxythiazole inhibitors of 5-lipoxygenase. |
Abbott Laboratories |
2016727 |
30 |
Novel caffeic acid derivatives: extremely potent inhibitors of 12-lipoxygenase. |
Institute For Bio-Medical Research |
1992126 |
54 |
Dual inhibitors of thromboxane A2 synthase and 5-lipoxygenase with scavenging activity of active oxygen species. Synthesis of a novel series of (3-pyridylmethyl)benzoquinone derivatives. |
Takeda Chemical Industries |
1903450 |
34 |
5-Lipoxygenase inhibitors: the synthesis and structure-activity relationships of a series of 1-phenyl-3-pyrazolidinones. |
Sterling Research Group |
1847426 |
56 |
Styrylpyrazoles, styrylisoxazoles, and styrylisothiazoles. Novel 5-lipoxygenase and cyclooxygenase inhibitors. |
Warner-Lambert |
1648621 |
55 |
(Methoxyalkyl)thiazoles: a new series of potent, selective, and orally active 5-lipoxygenase inhibitors displaying high enantioselectivity. |
Ici Pharmaceuticals Group |
1507204 |
18 |
Novel 1-(pyridylphenyl)-1-phenyl-2-imidazolylethanols with topical antiinflammatory activity. |
Dupont Pharmaceuticals |
1433212 |
59 |
Synthesis, chemical, and biological properties of vinylogous hydroxamic acids: dual inhibitors of 5-lipoxygenase and IL-1 biosynthesis. |
Dupont Pharmaceuticals |
1313879 |
21 |
Development of 2,3-dihydro-6-(3-phenoxypropyl)-2-(2-phenylethyl)-5-benzofuranol (L-670,630) as a potent and orally active inhibitor of 5-lipoxygenase. |
Merck Frosst Centre For Therapeutic Research |