65 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Discovery of 5-aryl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-ones as positive allosteric modulators of metabotropic glutamate subtype-2 (mGlu2) receptors with efficacy in a preclinical model of psychosis.

Merck Research Laboratories
Discovery of 2-[5-(4-Fluorophenylcarbamoyl)pyridin-2-ylsulfanylmethyl]phenylboronic Acid (SX-517): Noncompetitive Boronic Acid Antagonist of CXCR1 and CXCR2.

Syntrix Biosystems
Identification, biological characterization and pharmacophoric analysis of a new potent and selective NK1 receptor antagonist clinical candidate.

Glaxosmithkline
Cinnamides as selective small-molecule inhibitors of a cellular model of breast cancer stem cells.

Broad Institute of Mit and Harvard
Novel phomactin analogues as PAF receptor ligands.

The University of Nottingham
Designed multiple ligands. An emerging drug discovery paradigm.

Organon Laboratories
Structure-activity relationships of phomactin derivatives as platelet activating factor antagonists.

Sankyo
Synthesis of alkyl chain-modified ether lipids and evaluation of their in vitro cytotoxicity.

Laboratorios Menarini
Novel antagonists of platelet-activating factor. 2. Synthesis and structure-activity relationships of potent and long-acting heterofused [1,5]benzodiazepine and [1,4]diazepine derivatives of 2-methyl-1-phenylimidazo[4,5-c]pyridine.

Pfizer
Novel antagonists of platelet-activating factor. 1. Synthesis and structure-activity relationships of benzodiazepine and benzazepine derivatives of 2-methyl-1-phenylimidazo[4,5-c]pyridine.

Pfizer
3-(2-(3-Pyridinyl)thiazolidin-4-oyl)indoles, a novel series of platelet activating factor antagonists.

Abbott Laboratories
Design and modeling of new platelet-activating factor antagonists. 1. Synthesis and biological activity of 1,4-bis(3',4',5'-trimethoxybenzoyl)-2-[[(substituted carbonyl and carbamoyl)oxy]methyl]piperazines.

Paris Diderot University
Analogues of platelet activating factor. 6. Mono- and bis-aryl phosphate antagonists of platelet activating factor.

American Cyanamid
(Pyridylcyanomethyl)piperazines as orally active PAF antagonists.

J. Uriach & C£A.S.A.
Development, synthesis, and biological evaluation of (-)-trans-(2S,5S)-2-[3-[(2-oxopropyl)sulfonyl]-4-n-propoxy-5-(3- hydroxypropoxy)-phenyl]-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran, a potent orally active platelet-activating factor (PAF) antagonist and its water-soluble prodrug phosphate ester.

Merck Research Laboratories
1,4-Dihydropyridines as antagonists of platelet activating factor. 1. Synthesis and structure-activity relationships of 2-(4-heterocyclyl)phenyl derivatives.

Pfizer
4-Alkyl-1,4-dihydropyridines derivatives as specific PAF-acether antagonists.

Alter
Platelet activating factor antagonists: synthesis and structure-activity studies of novel PAF analogues modified in the phosphorylcholine moiety.

Takeda Chemical Industries
Structure-activity relationships of kadsurenone analogues.

TBA
A 3D-QSAR study on ginkgolides and their analogues with comparative molecular field analysis.

Chinese Academy of Sciences
Cyclic ether acetal platelet activating factor (PAF) receptor antagonists II: imidazo[4,5-c]pyridyl derivatives

TBA
Cyclic ether acetal platelet activating factor (PAF) receptor antagonists I: 3-pyridyl derivatives

TBA
A partial pharmacophore for the platelet activating factor (PAF) receptor

TBA
Synthesis and biological activity of the platelet-activating factor antagonist ()-trans-2-(3-methoxy-4-phenylsulfonylethoxy-5-n-propylsulfonylphenyl)-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran (L-671,284) and its analogs

TBA
Synthesis and biological activity of MK 287 (L-680,573): a potent, specific and orally active paf receptor antagonist

TBA
Cmi-206: A potent dual platelet activating factor antagonist and 5-lipoxygenase inhibitor

TBA
Enantiodifferentiation of dihydropyridine PAF antagonists

TBA
Synthesis and evaluation of water soluble indole pyrrolothiazole paf antagonists

TBA
Synthesis of active metabolites of indole pyrrolothiazole paf antagonists

TBA
Discovery and optimization of indole pyrrolothiazole paf antagonists

TBA
The discovery of CP-96,021 and CP-96,486, balanced, combined, potent and orally active leukotriene D
4 (LTD
4)/platelet activating factor (PAF) receptor antagonists.

TBA
Synthesis and bioactivities of heterocyclic lipids as PAF antagonists. 2

TBA
Synthesis and bioactivities of heterocyclic lipids as PAF antagonists. 1

TBA
Synthesis of bicyclic thiazolidine PAF antagonists

TBA
Cyclopentathiophene Carboxamide Derivatives as PAFR Antagonists for Treating Ocular Diseases, Allergies, and Inflammation-Related Disorders.

Smith, Gambrell & Russell
Discovery of a novel, orally active, small molecule gonadotropin-releasing hormone (GnRH) receptor antagonist.

Pfizer
Chemistry, biosynthesis and biological activity of terpenoids and meroterpenoids in bacteria and fungi isolated from different marine habitats.

Iranian Fisheries Science Research Institute
Preparation of 7-substituted ginkgolide derivatives: potent platelet activating factor (PAF) receptor antagonists.

Columbia University
Ginkgolide derivatives for photolabeling studies: preparation and pharmacological evaluation.

Columbia University
In vitro platelet-activating factor receptor binding inhibitory activity of pinusolide derivatives: a structure-activity study.

Seoul National University
(+/-)-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
Discovery and evaluation of a series of 3-acylindole imidazopyridine platelet-activating factor antagonists.

Abbott Laboratories
Analogues of platelet activating factor. 8. Antagonists of PAF containing an aromatic ring linked to a pyridinium ring.

American Cyanamid
Synthesis and structure-activity relationships of 1-acyl-4-((2-methyl-3-pyridyl)cyanomethyl)piperazines as PAF antagonists.

J. Uriach & CíA.
Structural modification of 5-aryl-2,3-dihydroimidazo[2,1-a]isoquinoline platelet activating factor receptor antagonists.

Sandoz Research Institute
Antitumor activity of 5-aryl-2,3-dihydroimidazo[2,1-a]isoquinolines.

Sandoz Research Institute
Development of a novel series of trialkoxyaryl derivatives as specific and competitive antagonists of platelet activating factor.

Wellcome Research Laboratories
Pyrido[2,1-b]quinazolinecarboxamide derivatives as platelet activating factor antagonists.

Hoffmann-La Roche
Conformation and activity of tetrahydrofuran lignans and analogues as specific platelet activating factor antagonists.

TBA
Pentadienyl carboxamide derivatives as antagonists of platelet-activating factor.

Roche Research Center
Biphenylcarboxamide derivatives as antagonists of platelet-activating factor.

Roche Research Center
Propenyl carboxamide derivatives as antagonists of platelet activating factor.

Hoffmann-La Roche
Thienotriazolodiazepines as platelet-activating factor antagonists. Steric limitations for the substituent in position 2.

Roche Research Center
Triazolobenzo- and triazolothienodiazepines as potent antagonists of platelet activating factor.

Roche Research Center
Disubstituted tetrahydrofurans and dioxolanes and PAF antagonists.

J. Uriach & CíA.
Dual antagonists of platelet activating factor and histamine. Identification of structural requirements for dual activity of N-Acyl-4-(5,6-dihydro-11H-benzo [5,6]cyclohepta-[1,2-b]pyridin-11-ylidene)piperidines.

Schering-Plough
4-substituted 2-alkoxytetrahydrofurans as potent and long-lasting PAF antagonists.

J. Uriach & CíA.
Synthesis and structure-activity relationships of a series of novel benzopyran-containing platelet activating factor antagonists.

Abbott Laboratories
Treatment of GVHD

Kadmon
Methods of use of cyclopamine analogs

Infinity Pharmaceuticals
Phenyl c-glucoside derivative containing deoxyglucose structure, preparation method and use thereof

Tianjin Institute of Pharmaceutical Research
Splicing factor SF3b as a target of the antitumor natural product pladienolide.

Eisai
The molecular structure of epoxide hydrolase B from Mycobacterium tuberculosis and its complex with a urea-based inhibitor.

University of Alberta