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SAR study on inhibitors of GIIA secreted phospholipase A2 using machine learning methods
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Design of new secreted phospholipase A2 inhibitors based on docking calculations by modifying the pharmacophore segments of the FPL67047XX inhibitor
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The Roles of the Secreted Phospholipase A2 Gene Family in Immunology
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Design of new potent and selective secretory phospholipase A2 inhibitors. Part 5: Synthesis and biological activity of 1-alkyl-4-[4,5-dihydro-1,2,4-[4H]-oxadiazol-5-one-3-ylmethylbenz-4′-yl(oyl)] piperazines
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Design of new potent and selective secretory phospholipase A2 inhibitors. 6-Synthesis, structure–activity relationships and molecular modelling of 1-substituted-4-[4,5-dihydro-1,2,4-(4H)-oxadiazol-5-one-3-yl(methyl)]-functionalized aryl piperazin/one/dione derivatives
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Inhibition of secreted phospholipases A2 by 2-oxoamides based on α-amino acids: Synthesis, in vitro evaluation and molecular docking calculations
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Quinoline-4-methyl esters as human nonpancreatic secretory phospholipase A2 inhibitors
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Development of a potent 2-oxoamide inhibitor of secreted phospholipase A2 guided by molecular docking calculations and molecular dynamics simulations
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Synthesis of phospholipase A2 inhibitory biflavonoids
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Simplified YM-26734 inhibitors of secreted phospholipase A2 group IIA
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Identification of inhibitors against interaction between pro-inflammatory sPLA2-IIA protein and integrin αvβ3
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Optimization of 5-hydroxytryptamines as dual function inhibitors targeting phospholipase A2 and leukotriene A4 hydrolase
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Synthesis of new secretory phospholipase A2-inhibitory indole containing isoxazole derivatives as anti-inflammatory and anticancer agents
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Celastrol modulates inflammation through inhibition of the catalytic activity of mediators of arachidonic acid pathway: Secretory phospholipase A 2 group IIA, 5-lipoxygenase and cyclooxygenase-2
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Expression of Group IIA Secretory Phospholipase A2 Is Elevated in Prostatic Intraepithelial Neoplasia and Adenocarcinoma
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Cloning and Recombinant Expression of Phospholipase A2 Present in Rheumatoid Arthritic Synovial Fluid
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Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
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Vinylogous hydroxamic acids: 5-lipoxygenase inhibitors
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Novel 3-dodecanoylindole-2-carboxylic acid inhibitors of cytosolic phospholipase A2
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Design and synthesis of new secretory phospholipase A2 inhibitor of a phospholipid analog
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ADMET Evaluation in Drug Discovery. 16. Predicting hERG Blockers by Combining Multiple Pharmacophores and Machine Learning Approaches
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ADMET Evaluation in Drug Discovery. 18. Reliable Prediction of Chemical-Induced Urinary Tract Toxicity by Boosting Machine Learning Approaches
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Molecular Docking and 3D-QSAR CoMFA Studies on Indole Inhibitors of GIIA Secreted Phospholipase A2
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Overcoming the Limitations of a Connection Table Description: A Universal Representation of Chemical Species
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Autocorrelation of Molecular Surface Properties for Modeling Corticosteroid Binding Globulin and Cytosolic Ah Receptor Activity by Neural Networks
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Carbocyclic[g]indole Inhibitors of Human Nonpancreatic s-PLA2
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Chemically Induced Dimerization of Human Nonpancreatic Secretory Phospholipase A2 by Bis-indole Derivatives
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Indole Inhibitors of Human Nonpancreatic Secretory Phospholipase A2. 2. Indole-3-acetamides with Additional Functionality
inferredcites →https://doi.org/10.1021/jm960487fopenalex-snapshot
Indole Inhibitors of Human Nonpancreatic Secretory Phospholipase A2. 3. Indole-3-glyoxamides
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Synthesis and Comparison of the Antiinflammatory Activity of Manoalide and Cacospongionolide B Analogues
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New Sesquiterpene Derivatives from the Sponge Dysidea Species with a Selective Inhibitor Profile against Human Phospholipase A2 and Other Leukocyte Functions
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A New Cacospongionolide Inhibitor of Human Secretory Phospholipase A2 from the Tyrrhenian Sponge Fasciospongia cavernosa and Absolute Configuration of Cacospongionolides
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Calculating partition coefficient by atom-additive method
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Gene Selection for Cancer Classification using Support Vector Machines
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Overexpression of group II phospholipase A2 in human breast cancer tissues is closely associated with their malignant potency
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Structure-based design of the first potent and selective inhibitor of human non-pancreatic secretory phospholipase A2
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Constructing and Validating High-Performance MIEC-SVM Models in Virtual Screening for Kinases: A Better Way for Actives Discovery
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Mechanism of Inhibition of Human Nonpancreatic Secreted Phospholipase A2 by the Anti-inflammatory Agent BMS-181162*
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A dendrite method for cluster analysis
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Inhibitors of phospholipase A2and their therapeutic potential: an update on patents (2012-2016)
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Randomized trial of an inhibitor of secretory phospholipase A2 on atherogenic lipoprotein subclasses in statin-treated patients with coronary heart disease
inferredcites →https://doi.org/10.1109/tpami.2002.1017616openalex-snapshot
An efficient k-means clustering algorithm: analysis and implementation
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Discovery of Novel Secretory Phospholipase A2Inhibitors Using Virtual Screen
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Increased group II phospholipase A2 in colonic mucosa of patients with Crohn's disease and ulcerative colitis.
inferredcites →https://doi.org/10.1159/000468890openalex-snapshot
Development of a Radioimmunoassay for Human Group-II Phospholipase A2 and Demonstration of Postoperative Elevation
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The sPLA2Inhibition to Decrease Enzyme Release After Percutaneous Coronary Intervention (SPIDER-PCI) Trial
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ADMET evaluation in drug discovery: 15. Accurate prediction of rat oral acute toxicity using relevance vector machine and consensus modeling
inferredcites →https://doi.org/10.1194/jlr.r058123openalex-snapshot
A new era of secreted phospholipase A2
inferredcites →https://doi.org/10.1194/jlr.r800033-jlr200openalex-snapshot
Phospholipase A2 structure/function, mechanism, and signaling
inferredcites →https://doi.org/10.1515/cclm.1987.25.8.505openalex-snapshot
Improved Method for the Determination of Phospholipase A2 Catalytic Activity Concentration in Human Serum and Ascites
inferredcites →https://doi.org/10.2174/092986705774462860openalex-snapshot
Inhibitors of Secretory Phospholipase A2 Group IIA
inferredcites →https://doi.org/10.4018/978-1-60566-766-9.ch015openalex-snapshot
Machine Learning Applications in Mega-Text Processing
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Phospholipase A2: A Potential Therapeutic Target in Inflammation and Cancer (In silico, In vitro, In vivo and Clinical Approach)
inferredcites →https://doi.org/10.7164/antibiotics.45.1071openalex-snapshot
A novel type of phospholipase A2 inhibitor, thielocin A1.BETA., and mechanism of action.
inferredcites →https://doi.org/10.7164/antibiotics.45.50openalex-snapshot
Cinatrins, a novel family of phospholipase A2 inhibitors. II. Biological activities.
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Isolation and Biological Activity of Thielocins: Novel Phospholipase A2 Inhibitors Produced by Thielavia terricola RF-143.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Systems biology approaches to unveiling the expression of phospholipases in various types of cancer—Transcriptomics and protein-protein interaction networks
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