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Cyclopentenone prostaglandins: New insights on biological activities and cellular targets

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inferredcites →https://doi.org/10.1002/(sici)1097-4644(19981101)71:2<254::aid-jcb10>3.0.co;2-lopenalex-snapshot
Role of EP2 receptors and cAMP in prostaglandin E2 regulated expression of type I collagen α1, lysyl oxidase, and cyclooxygenase-1 genes in human embryo lung fibroblasts
inferredcites →https://doi.org/10.1002/anie.199104553openalex-snapshot
The Logic of Chemical Synthesis: Multistep Synthesis of Complex Carbogenic Molecules (Nobel Lecture)
inferredcites →https://doi.org/10.1002/bms.1200150105openalex-snapshot
Rapid quantification of 11 prostanoids by combined capillary column gas chromatography and negative ion chemical ionization mass spectrometry: Application to prostanoids released from normal human embryonic lung fibroblasts WI38 in a culture medium
inferredcites →https://doi.org/10.1002/j.1460-2075.1993.tb05994.xopenalex-snapshot
Chromatin disruption in the promoter of human immunodeficiency virus type 1 during transcriptional activation.
inferredcites →https://doi.org/10.1002/jcp.1041140203openalex-snapshot
Loss of the PGE1 requirement for MDCK cell growth associated with a defect in cyclic AMP phosphodiesterase
inferredcites →https://doi.org/10.1002/jlb.66.5.733openalex-snapshot
The peroxisome proliferator-activated receptorγ (PPARγ) as a regulator of monocyte/macrophage function
inferredcites →https://doi.org/10.1006/bbrc.1996.0393openalex-snapshot
Induction of Protein Disulfide Isomerase mRNA by Δ12-Prostaglandin J2
inferredcites →https://doi.org/10.1006/excr.1993.1188openalex-snapshot
Induction of Thermotolerance by Prostaglandin A in Human Cells
inferredcites →https://doi.org/10.1007/978-1-4615-4793-8_1openalex-snapshot
Function and Regulation of Prostaglandin Synthase 2
inferredcites →https://doi.org/10.1007/bf00666101openalex-snapshot
Preclinical studies of antitumor prostaglandins by using human ovarian cancer cells
inferredcites →https://doi.org/10.1007/bf00744216openalex-snapshot
Induction ofMRP/GS-X pump and cellular resistance to anticancer prostaglandins
inferredcites →https://doi.org/10.1007/bf01311026openalex-snapshot
Antiviral activity of a synthetic analog of prostaglandin A in mice infected with influenza A virus
inferredcites →https://doi.org/10.1007/bf01629429openalex-snapshot
Adjuvant effects of antineoplastic prostaglandins to cisplatin in nude mice bearing human ovarian cancer cells
inferredcites →https://doi.org/10.1016/0003-2697(76)90354-7openalex-snapshot
Method for quantitative analysis of PGA2 from plasma using deuterated carrier and gas-liquid chromatography-mass spectrometry
inferredcites →https://doi.org/10.1016/0005-2760(75)90184-8openalex-snapshot
The conjugation of prostaglandin A1 and glutathione catalyzed by homogeneous glutathione S-transferases from human and rat liver
inferredcites →https://doi.org/10.1016/0006-291x(82)91063-4openalex-snapshot
Prostaglandin D2, a potential antineoplastic agent
inferredcites →https://doi.org/10.1016/0006-291x(82)91986-6openalex-snapshot
9-Deoxy-Δ9-prostaglandin D2, a prostaglandin D2 derivative with potent antineoplastic and weak smooth muscle-contracting activities
inferredcites →https://doi.org/10.1016/0006-291x(85)91398-1openalex-snapshot
Requirement of a reactive α,β-unsaturated carbonyl for inhibition of tumor growth and induction of differentiation by “A” series prostaglandins
inferredcites →https://doi.org/10.1016/0006-291x(87)90809-6openalex-snapshot
Mechanism of inhibition of herpes simplex virus replication by Δ7-prostaglandin A1 and Δ12-prostaglandin J2
inferredcites →https://doi.org/10.1016/0006-291x(90)92356-5openalex-snapshot
Induction of γ-glutamylcysteine synthetase by prostaglandin A2 in L-1210 cells
inferredcites →https://doi.org/10.1016/0006-2952(92)90612-mopenalex-snapshot
Formation of a prostaglandin A2-glutathione conjugate in L1210 mouse leukemia cells
inferredcites →https://doi.org/10.1016/0014-4827(84)90358-6openalex-snapshot
Effects of bradykinin on DNA synthesis in resting NIL8 hamster cells and human fibroblasts
inferredcites →https://doi.org/10.1016/0014-4827(92)90464-jopenalex-snapshot
Cell growth inhibition by prostaglandin A2 results in elevated expression of gadd153 mRNA
inferredcites →https://doi.org/10.1016/0014-5793(90)81224-copenalex-snapshot
N‐myc suppression and cell cycle arrest at G1 phase by prostaglandins
inferredcites →https://doi.org/10.1016/0014-5793(95)01001-uopenalex-snapshot
Involvement of protein kinase in Δ12‐prostaglandin J2‐induced expression of rat heme oxygenase‐1 gene
inferredcites →https://doi.org/10.1016/0090-6980(75)90103-3openalex-snapshot
Assessment of the levels of PGA2 in human plasma by gas chromatography-mass spectrometry
inferredcites →https://doi.org/10.1016/0090-6980(76)90167-2openalex-snapshot
High performance liquid chromatography of prostaglandins: Biological applications
inferredcites →https://doi.org/10.1016/0090-6980(89)90096-8openalex-snapshot
Levuglandin E2 crosslinks proteins
inferredcites →https://doi.org/10.1016/0090-6980(96)00047-0openalex-snapshot
Intracellular glutathione level modulates the induction of apoptosis by Δ12-prostaglandin J2
inferredcites →https://doi.org/10.1016/0092-8674(95)90193-0openalex-snapshot
15-Deoxy-Δ12,14-Prostaglandin J2 is a ligand for the adipocyte determination factor PPARγ
inferredcites →https://doi.org/10.1016/0092-8674(95)90194-9openalex-snapshot
A prostaglandin J2 metabolite binds peroxisome proliferator-activated receptor γ and promotes adipocyte differentiation
inferredcites →https://doi.org/10.1016/0163-7258(91)90054-popenalex-snapshot
Prostaglandin and thromboxane biosynthesis
inferredcites →https://doi.org/10.1016/0163-7827(81)90147-8openalex-snapshot
Endogenous prostaglandin as (PGAs): Fact or artifact in biological systems
inferredcites →https://doi.org/10.1016/0166-3542(93)90020-jopenalex-snapshot
Inhibition of vesicular stomatitis virus replication by Δ12-prostaglandin J2 is regulated at two separate levels and is associated with induction of stress protein synthesis
inferredcites →https://doi.org/10.1016/0166-3542(93)90021-aopenalex-snapshot
Inhibition of Sindbis virus replication by cyclopentenone prostaglandins: A cell-mediated event associated with heat-shock protein synthesis
inferredcites →https://doi.org/10.1016/0262-1746(84)90066-0openalex-snapshot
On the identification and biological properties of prostaglandin J2
inferredcites →https://doi.org/10.1016/s0005-2760(96)00162-2openalex-snapshot
The generation and actions of isoprostanes
inferredcites →https://doi.org/10.1016/s0005-2760(98)00168-4openalex-snapshot
Evidence for the formation of a novel cyclopentenone isoprostane, 15-A2t-isoprostane (8-iso-prostaglandin A2) in vivo
inferredcites →https://doi.org/10.1016/s0006-291x(86)80062-6openalex-snapshot
Metabolic dehydration of prostaglandin E2 and cellular uptake of the dehydration product: Correlation with prostaglandin E2-induced growth inhibition
inferredcites →https://doi.org/10.1016/s0006-2952(99)00048-9openalex-snapshot
Interactions of prostaglandin A2 with the glutathione-mediated biotransformation system
inferredcites →https://doi.org/10.1016/s0006-2952(99)00299-3openalex-snapshot
Heat shock factors and the control of the stress response
inferredcites →https://doi.org/10.1016/s0014-5793(97)01442-7openalex-snapshot
Transport of glutathione prostaglandin A conjugates by the multidrug resistance protein 1
inferredcites →https://doi.org/10.1016/s0021-9258(17)32107-5openalex-snapshot
Protein-DNA interactions within DNase I-hypersensitive sites located downstream of the HIV-1 promoter.
inferredcites →https://doi.org/10.1016/s0021-9258(17)44287-6openalex-snapshot
Albumin-catalyzed metabolism of prostaglandin D2. Identification of products formed in vitro.
inferredcites →https://doi.org/10.1016/s0021-9258(18)33282-4openalex-snapshot
Evidence for cAMP-independent inhibition of S-phase DNA synthesis by prostaglandins.
inferredcites →https://doi.org/10.1016/s0021-9258(18)37435-0openalex-snapshot
Occurrence of 9-deoxy-delta 9,delta 12-13,14-dihydroprostaglandin D2 in human urine.
inferredcites →https://doi.org/10.1016/s0021-9258(18)45277-5openalex-snapshot
Depletion of intracellular calcium stores by calcium ionophore A23187 induces the genes for glucose-regulated proteins in hamster fibroblasts.
inferredcites →https://doi.org/10.1016/s0021-9258(18)96910-3openalex-snapshot
Prostaglandins in Human Seminal Plasma
inferredcites →https://doi.org/10.1016/s0022-2275(20)40657-1openalex-snapshot
Prostaglandin synthesis in rat adrenocortical cells.
inferredcites →https://doi.org/10.1016/s0040-4020(01)85596-4openalex-snapshot
Three-component coupling synthesis of prostaglandins. A simplified, general procedure
inferredcites →https://doi.org/10.1016/s0040-4020(97)10151-xopenalex-snapshot
Δ7-Prostaglandin C1: A primary metabolite of antitumor Δ7-prostaglandin A1 in the sera
inferredcites →https://doi.org/10.1016/s0083-6729(00)58022-4openalex-snapshot
Prostaglandin D synthase: Structure and function
inferredcites →https://doi.org/10.1016/s0090-6980(96)00093-7openalex-snapshot
Induction of c-fos protooncogene transcription and apoptosis by Δ12-prostaglandin J2 in human Pl-21 myeloid leukemia and RC-K8 pre-B lymphoma cells
inferredcites →https://doi.org/10.1016/s0090-9556(25)08971-8openalex-snapshot
Identification of the major metabolites of the prostaglandin E2-analogue sulprostone in human plasma, and isolation from urine (in vivo) and liver perfusate (in vitro) of female guinea-pigs.
inferredcites →https://doi.org/10.1016/s0092-8674(00)80374-8openalex-snapshot
Cloning and Crystal Structure of Hematopoietic Prostaglandin D Synthase
inferredcites →https://doi.org/10.1016/s0092-8674(00)80855-7openalex-snapshot
Tripartite Management of Unfolded Proteins in the Endoplasmic Reticulum
inferredcites →https://doi.org/10.1016/s0092-8674(00)81118-6openalex-snapshot
A CBP Integrator Complex Mediates Transcriptional Activation and AP-1 Inhibition by Nuclear Receptors
inferredcites →https://doi.org/10.1016/s0092-8674(00)81375-6openalex-snapshot
Dissection of TNF Receptor 1 Effector Functions: JNK Activation Is Not Linked to Apoptosis While NF-κB Activation Prevents Cell Death
inferredcites →https://doi.org/10.1016/s0167-4781(97)00214-5openalex-snapshot
Effects of cyclopentenone prostaglandins and related compounds on insulin-like growth factor-I and Waf1 gene expression
inferredcites →https://doi.org/10.1016/s0304-419x(97)00018-8openalex-snapshot
Regulation and function of the JNK subgroup of MAP kinases
inferredcites →https://doi.org/10.1016/s0952-3278(98)90039-4openalex-snapshot
Induction of apoptosis, p53 and heme oxygenase-1 by cytotoxic prostaglandin Δ12-PGJ2 in transformed endothelial cells
inferredcites →https://doi.org/10.1016/s0966-842x(97)01066-4openalex-snapshot
Antiviral activity of cyclopentenone prostanoids
inferredcites →https://doi.org/10.1016/s1097-2765(00)80467-0openalex-snapshot
Molecular Recognition of Fatty Acids by Peroxisome Proliferator–Activated Receptors
inferredcites →https://doi.org/10.1021/bi00066a034openalex-snapshot
Formation of DNA-protein cross-links in mammalian cells by levuglandin E2
inferredcites →https://doi.org/10.1021/bi00467a023openalex-snapshot
Formation of thiol conjugates of 9-deoxy-.DELTA.9,.DELTA.12(E)-prostaglandin D2 and .DELTA.12(E)-prostaglandin D2
inferredcites →https://doi.org/10.1021/bi990470+openalex-snapshot
Characterization of the Lysyl Adducts Formed from Prostaglandin H2 via the Levuglandin Pathway
inferredcites →https://doi.org/10.1021/jm9801657openalex-snapshot
Rational Design of Antitumor Prostaglandins with High Biological Stability
inferredcites →https://doi.org/10.1021/tx9601770openalex-snapshot
Stereoselective Conjugation of Prostaglandin A 2 and Prostaglandin J 2 with Glutathione, Catalyzed by the Human Glutathione S -Transferases A1-1, A2-2, M1a-1a, and P1-1
inferredcites →https://doi.org/10.1038/25931openalex-snapshot
Ligand binding and co-activator assembly of the peroxisome proliferator-activated receptor-γ
inferredcites →https://doi.org/10.1038/263777a0openalex-snapshot
Inhibition of tumour growth in vivo and in vitro by prostaglandin E
inferredcites →https://doi.org/10.1038/34178openalex-snapshot
The peroxisome proliferator-activated receptor-γ is a negative regulator of macrophage activation
inferredcites →https://doi.org/10.1038/34184openalex-snapshot
PPAR-γ agonists inhibit production of monocyte inflammatory cytokines
inferredcites →https://doi.org/10.1038/35013000openalex-snapshot
Roles of PPARs in health and disease
inferredcites →https://doi.org/10.1038/47520openalex-snapshot
Anti-inflammatory cyclopentenone prostaglandins are direct inhibitors of IκB kinase
inferredcites →https://doi.org/10.1038/9550openalex-snapshot
Inducible cyclooxygenase may have anti-inflammatory properties
inferredcites →https://doi.org/10.1038/sj.bjp.0701708openalex-snapshot
Characterization of the recombinant human prostanoid DP receptor and identification of L‐644,698, a novel selective DP agonist
inferredcites →https://doi.org/10.1039/c39790000679openalex-snapshot
Synthesis of 9-deoxa-9,10-dehydroprostaglandin-D2 through reaction of 2-oxatricyclo[3.3.0.04,6]oct-7-en-3-one with a cuprate reagent
inferredcites →https://doi.org/10.1042/bj1051251openalex-snapshot
The identification of prostaglandins E2, F2α and A2 from rabbit kidney medulla
inferredcites →https://doi.org/10.1042/bj3080455openalex-snapshot
Induction by prostaglandin A1 of haem oxygenase in myoblastic cells: an effect independent of expression of the 70 kDa heat shock protein
inferredcites →https://doi.org/10.1042/bj3350035openalex-snapshot
Localization of a cyclopentenone prostaglandin to the endoplasmic reticulum and induction of BiP mRNA
inferredcites →https://doi.org/10.1042/bj3360569openalex-snapshot
Anti-cancer-prostaglandin-induced cell-cycle arrest and its modulation by an inhibitor of the ATP-dependent glutathione S-conjugate export pump (GS-X pump)
inferredcites →https://doi.org/10.1046/j.1432-1327.1999.00610.xopenalex-snapshot
Induction of ferritin and heat shock proteins by prostaglandin A1 in human monocytes
inferredcites →https://doi.org/10.1073/pnas.72.7.2724openalex-snapshot
Initiation of cell proliferation in cultured mouse fibroblasts by prostaglandin F2alpha.
inferredcites →https://doi.org/10.1073/pnas.76.7.3338openalex-snapshot
Growth of Madin-Darby canine kidney epithelial cell (MDCK) line in hormone-supplemented, serum-free medium.
inferredcites →https://doi.org/10.1073/pnas.79.16.4992openalex-snapshot
Prostaglandins E1 and E2 interact with prostaglandin F2alpha to regulate initiation of DNA replication and cell division in swiss 3T3 cells.
inferredcites →https://doi.org/10.1073/pnas.81.5.1317openalex-snapshot
9-Deoxy-delta 9, delta 12-13,14-dihydroprostaglandin D2, a metabolite of prostaglandin D2 formed in human plasma.
inferredcites →https://doi.org/10.1073/pnas.89.14.6227openalex-snapshot
Antiproliferative prostaglandins activate heat shock transcription factor.
inferredcites →https://doi.org/10.1073/pnas.94.2.746openalex-snapshot
Inhibition of nuclear factor κB by prostaglandin A 1 : An effect associated with heat shock transcription factor activation
inferredcites →https://doi.org/10.1073/pnas.94.9.4312openalex-snapshot
Hypolipidemic drugs, polyunsaturated fatty acids, and eicosanoids are ligands for peroxisome proliferator-activated receptors α and δ
inferredcites →https://doi.org/10.1073/pnas.96.8.4668openalex-snapshot
Cyclopentenone prostaglandins suppress activation of microglia: Down-regulation of inducible nitric-oxide synthase by 15-deoxy-Δ 12,14 -prostaglandin J 2
inferredcites →https://doi.org/10.1073/pnas.97.9.4844openalex-snapshot
15-Deoxy-Δ 12,14 -prostaglandin J 2 inhibits multiple steps in the NF-κB signaling pathway
inferredcites →https://doi.org/10.1074/jbc.270.28.16483openalex-snapshot
The Regulation of AP-1 Activity by Mitogen-activated Protein Kinases
inferredcites →https://doi.org/10.1074/jbc.270.37.21779openalex-snapshot
Identification of a cis-Regulatory Element for Δ12-Prostaglandin J2-induced Expression of the Rat Heme Oxygenase Gene
inferredcites →https://doi.org/10.1074/jbc.270.41.23975openalex-snapshot
Differential Activation of Peroxisome Proliferator-activated Receptors by Eicosanoids
inferredcites →https://doi.org/10.1074/jbc.271.1.32openalex-snapshot
Characterization of the Essential Gene glmM Encoding Phosphoglucosamine Mutase in Escherichia coli
inferredcites →https://doi.org/10.1074/jbc.271.28.16609openalex-snapshot
Regulation of BiP Gene Expression by Cyclopentenone Prostaglandins through Unfolded Protein Response Element
inferredcites →https://doi.org/10.1074/jbc.271.50.32192openalex-snapshot
2-Cyclopenten-1-one, a New Inducer of Heat Shock Protein 70 with Antiviral Activity
inferredcites →https://doi.org/10.1074/jbc.274.16.10863openalex-snapshot
Formation of Reactive Cyclopentenone Compounds in Vivo as Products of the Isoprostane Pathway
inferredcites →https://doi.org/10.1074/jbc.274.24.17042openalex-snapshot
Endothelial Cell Apoptosis Induced by the Peroxisome Proliferator-activated Receptor (PPAR) Ligand 15-Deoxy-Δ12,14-prostaglandin J2
inferredcites →https://doi.org/10.1074/jbc.274.29.20271openalex-snapshot
Protein Adducts of Iso[4]levuglandin E2, a Product of the Isoprostane Pathway, in Oxidized Low Density Lipoprotein
inferredcites →https://doi.org/10.1074/jbc.275.15.11291openalex-snapshot
Cyclopentenone Prostaglandins as Potential Inducers of Phase II Detoxification Enzymes
inferredcites →https://doi.org/10.1080/09629359891216openalex-snapshot
Release of prostaglandin D2 by murine mast cells: importance of metabolite formation for antiproliferative activity
inferredcites →https://doi.org/10.1093/jnci/47.6.1357openalex-snapshot
Change in Growth and Morphology of Fibroblasts by Prostaglandins
inferredcites →https://doi.org/10.1093/nar/28.3.663openalex-snapshot
SURVEY AND SUMMARY A compilation of cellular transcription factor interactions with the HIV-1 LTR promoter
inferredcites →https://doi.org/10.1096/fasebj.8.13.7926370openalex-snapshot
Calcium mediates expression of stress‐response genes in prostaglandin A 2 ‐induced growth arrest
inferredcites →https://doi.org/10.1097/00001813-199404000-00002openalex-snapshot
Prostaglandins in the treatment of cancer
inferredcites →https://doi.org/10.1097/00041433-199906000-00007openalex-snapshot
Peroxisome proliterator-activated receptor-alpha activators regulate genes governing lipoprotein metabolism, vascular inflammation and atherosclerosis
inferredcites →https://doi.org/10.1099/0022-1317-63-2-435openalex-snapshot
Antiviral Effect of Prostaglandins of the A Series: Inhibition of Vaccinia Virus Replication in Cultured Cells
inferredcites →https://doi.org/10.1099/0022-1317-64-12-2797openalex-snapshot
Prostaglandin A Inhibits the Replication of Vesicular Stomatitis Virus: Effect on Virus Glycoprotein
inferredcites →https://doi.org/10.1099/0022-1317-66-11-2355openalex-snapshot
Antiviral Activity of Prostaglandin A on Encephalomyocarditis Virus-infected Cells: A Unique Effect Unrelated to Interferon
inferredcites →https://doi.org/10.1099/0022-1317-70-4-789openalex-snapshot
Inhibition of Virus Protein Glycosylation as the Mechanism of the Antiviral Action of Prostaglandin A in Sendai Virus-infected Cells
inferredcites →https://doi.org/10.1099/0022-1317-71-12-2823openalex-snapshot
Inhibition of Primary Transcription of Vesicular Stomatitis Virus by Prostaglandin A1
inferredcites →https://doi.org/10.1099/0022-1317-72-11-2797openalex-snapshot
Prostaglandin A inhibits replication of human immunodeficiency virus during acute infection
inferredcites →https://doi.org/10.1099/0022-1317-72-8-1877openalex-snapshot
Suppression Of Virus Replication By Prostaglandin A Is Associated With Heat Shock Protein Synthesis
inferredcites →https://doi.org/10.1101/gad.10.1.37openalex-snapshot
NF-kappa B-mediated chromatin reconfiguration and transcriptional activation of the HIV-1 enhancer in vitro.
inferredcites →https://doi.org/10.1101/gad.11.24.3327openalex-snapshot
Histone acetyltransferases regulate HIV-1 enhancer activity in vitro
inferredcites →https://doi.org/10.1101/gad.14.11.1293openalex-snapshot
Transcriptional regulation of adipogenesis
inferredcites →https://doi.org/10.1101/gad.14.2.121openalex-snapshot
The coregulator exchange in transcriptional functions of nuclear receptors
inferredcites →https://doi.org/10.1111/j.1476-5381.1985.tb08870.xopenalex-snapshot
Different responsiveness of prostaglandin D2‐sensitive systems to prostaglandin D2 and its analogues
inferredcites →https://doi.org/10.1111/j.1749-6632.1971.tb53194.xopenalex-snapshot
HYPERTENSION AND THE RENOMEDULLARY PROSTAGLANDINS: A HUMAN STUDY OF THE ANTIHYPERTENSIVE EFFECTS OF PGA 1
inferredcites →https://doi.org/10.1111/j.1749-6632.1994.tb52733.xopenalex-snapshot
Prostaglandin J2 and Related Compounds
inferredcites →https://doi.org/10.1126/science.6157190openalex-snapshot
Prostaglandin A Compounds as Antiviral Agents
inferredcites →https://doi.org/10.1126/science.8418493openalex-snapshot
Organic Synthesis of Prostaglandins: Advancing Biology
inferredcites →https://doi.org/10.1126/science.877555openalex-snapshot
Fatty Acids and Their Prostaglandin Derivatives: Inhibitors of Proliferation in Aortic Smooth Muscle Cells
inferredcites →https://doi.org/10.1128/aac.36.10.2253openalex-snapshot
Effects of dimethyl prostaglandin A1 on herpes simplex virus and human immunodeficiency virus replication
inferredcites →https://doi.org/10.1128/aac.40.2.367openalex-snapshot
Inhibition of poliovirus replication by prostaglandins A and J in human cells
inferredcites →https://doi.org/10.1128/mcb.12.4.1528openalex-snapshot
Induction of HSP70 Gene Expression by the Antiproliferative Prostaglandin PGA 2 : A Growth-Dependent Response Mediated by Activation of Heat Shock Transcription Factor
inferredcites →https://doi.org/10.1128/mcb.12.7.3094openalex-snapshot
The RxxRxRxxC motif conserved in all Rel/kappa B proteins is essential for the DNA-binding activity and redox regulation of the v-Rel oncoprotein.
inferredcites →https://doi.org/10.1128/mcb.13.2.852openalex-snapshot
N-terminal DNA-binding domains contribute to differential DNA-binding specificities of NF-kappa B p50 and p65.
inferredcites →https://doi.org/10.1128/mcb.13.6.3782openalex-snapshot
Fos is a Preferential Target of Glucocorticoid Receptor Inhibition of AP-1 Activity In Vitro
inferredcites →https://doi.org/10.1128/mcb.16.3.762openalex-snapshot
Inhibition of G 1 Cyclin-Dependent Kinase Activity during Growth Arrest of Human Breast Carcinoma Cells by Prostaglandin A 2
inferredcites →https://doi.org/10.1128/mcb.20.13.4699-4707.2000openalex-snapshot
Peroxisome Proliferator-Activated Receptor γ-Dependent Repression of the Inducible Nitric Oxide Synthase Gene
inferredcites →https://doi.org/10.1128/mcb.20.5.1626-1638.2000openalex-snapshot
Akt Suppresses Apoptosis by Stimulating the Transactivation Potential of the RelA/p65 Subunit of NF-κB
inferredcites →https://doi.org/10.1128/mcb.20.5.1692-1698.2000openalex-snapshot
Inhibition of IκB Kinase and IκB Phosphorylation by 15-Deoxy-Δ12,14-Prostaglandin J2 in Activated Murine Macrophages
inferredcites →https://doi.org/10.1146/annurev.immunol.16.1.225openalex-snapshot
NF-κB AND REL PROTEINS: Evolutionarily Conserved Mediators of Immune Responses
inferredcites →https://doi.org/10.1146/annurev.immunol.18.1.621openalex-snapshot
Phosphorylation Meets Ubiquitination: The Control of NF-κB Activity
inferredcites →https://doi.org/10.1161/01.res.17.1.57openalex-snapshot
Renomedullary Vasodepressor Substance, Medullin
inferredcites →https://doi.org/10.1172/jci108758openalex-snapshot
Prostaglandin biosynthesis by rabbit renomedullary interstitial cells in tissue culture. Stimulation by angiotensin II, bradykinin, and arginine vasopressin.
inferredcites →https://doi.org/10.1172/jci118609openalex-snapshot
Inhibition of HIV-1 replication by cyclopentenone prostaglandins in acutely infected human cells. Evidence for a transcriptional block.
inferredcites →https://doi.org/10.1210/en.138.3.985openalex-snapshot
Prostaglandin A2 Specifically Represses Insulin-Like Growth Factor-I Gene Expression in C6 Rat Glioma Cells
inferredcites →https://doi.org/10.1210/jcem-41-2-245openalex-snapshot
A Radioimmunoassay for Prostaglandin A1in Human Peripheral Blood*
inferredcites →https://doi.org/10.1248/cpb.32.4658openalex-snapshot
Synthesis of new antineoplastic prostaglandins.
inferredcites →https://doi.org/10.3109/07853899908995901openalex-snapshot
Peroxisome proliferator-activated receptor-γ: a versatile metabolic regulator
inferredcites →https://doi.org/10.3109/10409239509083491openalex-snapshot
The Glut athione S-Transferase Supergene Family: Regulation of GST and the Contribution of the lsoenzymes to Cancer Chemoprotection and Drug Resistance Part I
inferredcites →https://doi.org/10.3181/00379727-166-41109openalex-snapshot
Prostaglandin Analogs as Inhibitors of Tumor Cell DNA Synthesis
inferredcites →https://doi.org/10.4049/jimmunol.138.10.3094openalex-snapshot
Prostaglandin synthesis in human T cells: its partial inhibition by lectins and anti-CD3 antibodies as a possible step in T cell activation.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4785543openalex-extracted
Impact of Overexpression of Wild-Type Cftr and Elexacaftor-Texacaftor-Ivacaftor on Oxylipin Production by Cystic Fibrosis Bronchial Epithelial Cells
inferred← citeshttps://doi.org/10.1002/0471266949.bmc064.pub2openalex-snapshot
Agents Acting on Prostanoid and Thromboxane Receptors
inferred← citeshttps://doi.org/10.1002/9780470753064.ch26openalex-snapshot
Adjuvant Approaches for Preventing Brain Metastases
inferred← citeshttps://doi.org/10.1002/9781118355886.ch10openalex-snapshot
Neurodegeneration from Drugs and Aging‐Derived Free Radicals
inferred← citeshttps://doi.org/10.1002/9781119949091.ch4openalex-snapshot
Regulation of Acclimation to Environmental Stress
inferred← citeshttps://doi.org/10.1002/ana.10668openalex-snapshot
Cyclooxygenase‐2 and stroke: The long and short of it
inferred← citeshttps://doi.org/10.1002/ange.200462235openalex-snapshot
Die intermolekulare Pauson‐Khand‐Reaktion
inferred← citeshttps://doi.org/10.1002/ange.201408364openalex-snapshot
Nickel(0)‐Catalyzed Enantioselective Annulations of Alkynes and Arylenoates Enabled by a Chiral NHC Ligand: Efficient Access to Cyclopentenones
inferred← citeshttps://doi.org/10.1002/anie.200462235openalex-snapshot
The Intermolecular Pauson–Khand Reaction
inferred← citeshttps://doi.org/10.1002/anie.201408364openalex-snapshot
Nickel(0)‐Catalyzed Enantioselective Annulations of Alkynes and Arylenoates Enabled by a Chiral NHC Ligand: Efficient Access to Cyclopentenones
inferred← citeshttps://doi.org/10.1002/art.20104openalex-snapshot
Disruption of transforming growth factor β signaling and profibrotic responses in normal skin fibroblasts by peroxisome proliferator–activated receptor γ
inferred← citeshttps://doi.org/10.1002/biof.5520290103openalex-snapshot
NF‐κB as a potential molecular target for cancer therapy
inferred← citeshttps://doi.org/10.1002/bit.27792openalex-snapshot
Prostaglandin production by the microalga with heterologous expression of cyclooxygenase
inferred← citeshttps://doi.org/10.1002/cbic.200400259openalex-snapshot
Total Synthesis and Biological Activity of 13,14‐Dehydro‐12‐Oxo‐Phytodienoic Acids (Deoxy‐J1‐Phytoprostanes)
inferred← citeshttps://doi.org/10.1002/cbic.200600379openalex-snapshot
Rapid Enzymatic Isomerization of 12‐Oxophytodienoic Acid in the Gut of Lepidopteran Larvae
inferred← citeshttps://doi.org/10.1002/cctc.200900269openalex-snapshot
One‐Pot Synthesis of Bicyclic Fused Cyclopentenone Derivatives from 1‐Ethynylcycloalkanols and Aldehydes
inferred← citeshttps://doi.org/10.1002/chin.200127239openalex-snapshot
ChemInform Abstract: Cyclopentenone Prostaglandins: New Insights on Biological Activities and Cellular Targets
inferred← citeshttps://doi.org/10.1002/cphy.c100077openalex-snapshot
Cyclooxygenase Metabolites in the Kidney
inferred← citeshttps://doi.org/10.1002/cti2.1104openalex-snapshot
UV radiation recruits CD4+GATA3+ and CD8+GATA3+ T cells while altering the lipid microenvironment following inflammatory resolution in human skin in vivo
inferred← citeshttps://doi.org/10.1002/ejlt.201800484openalex-snapshot
The Value of Legume Foods as a Dietary Source of Phytoprostanes and Phytofurans Is Dependent on Species, Variety, and Growing Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.200300045openalex-snapshot
Domino Aza‐Claisen/Mannich Cyclization Reaction from a Chiral α‐Alkoxy Enamine or Sequential Alkylation of an α‐Alkoxy Ester Enolate or Nitrile Anion, Followed by an Intramolecular Wittig Reaction: Two (3+2) Annulation Routes to Homochiral 4‐Alkyl‐4‐hydroxy‐2‐cyclopentenone Synthesis
inferred← citeshttps://doi.org/10.1002/ejoc.200800488openalex-snapshot
The Intermolecular Pauson–Khand Reaction of meso‐Substituted Porphyrins
inferred← citeshttps://doi.org/10.1002/ejoc.201000704openalex-snapshot
Chemistry of 4‐Hydroxy‐2‐cyclopentenone Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.201900102openalex-snapshot
Concise Synthesis of a New Chiral Cyclopentenone Building Block for Prostaglandins and their Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.202001218openalex-snapshot
Synthesis of Fluorine‐Containing 3‐Aminocyclopent‐2‐enones via Intramolecular Cyclization
inferred← citeshttps://doi.org/10.1002/glia.20658openalex-snapshot
Regulation of prostaglandin E2 synthase expression in activated primary rat microglia: Evidence for uncoupled regulation of mPGES‐1 and COX‐2
inferred← citeshttps://doi.org/10.1002/ijc.24004openalex-snapshot
Induction of the lysosomal apoptosis pathway by inhibitors of the ubiquitin‐proteasome system
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2011.tb00382.xopenalex-snapshot
Cyclooxygenase Metabolites in the Kidney
inferred← citeshttps://doi.org/10.1002/jcp.10250openalex-snapshot
15‐deoxy‐Δ12,14 prostaglandin J2 synergizes with phorbol ester to induce proliferation in Swiss 3T3 cells independently of peroxisome proliferator‐activated receptor gamma and PGD2 receptors
inferred← citeshttps://doi.org/10.1002/jnr.10501openalex-snapshot
Effects of peroxisome proliferator‐activated receptor‐γ agonists on central nervous system inflammation
inferred← citeshttps://doi.org/10.1002/jnr.20413openalex-snapshot
Cyclopentenone prostaglandins PGA2 and 15-deoxy-?12,14 PGJ2 suppress activation of murine microglia and astrocytes: Implications for multiple sclerosis
inferred← citeshttps://doi.org/10.1002/jnr.21049openalex-snapshot
Heme oxygenase and cyclooxygenase in the central nervous system: A functional interplay
inferred← citeshttps://doi.org/10.1002/jnr.21569openalex-snapshot
Neuroprotective effects of prostaglandin A1in rat models of permanent focal cerebral ischemia are associated with nuclear factor‐κB inhibition and peroxisome proliferator‐activated receptor‐γ up‐regulation
inferred← citeshttps://doi.org/10.1002/jsfa.11345openalex-snapshot
Phytoprostanes, phytofurans, tocopherols, tocotrienols, carotenoids and free amino acids and biological potential of sea buckthorn juices
inferred← citeshttps://doi.org/10.1002/mas.21383openalex-snapshot
Modification of cysteine residues by cyclopentenone prostaglandins: Interplay with redox regulation of protein function
inferred← citeshttps://doi.org/10.1002/mco2.728openalex-snapshot
Lymphatic‐specific methyltransferase‐like 3‐mediated m6A modification drives vascular patterning through prostaglandin metabolism reprogramming
inferred← citeshttps://doi.org/10.1002/pmic.201200289openalex-snapshot
Proteomic identification of the candidate target proteins of 15‐deoxy‐delta12,14‐prostaglandin J 2
inferred← citeshttps://doi.org/10.1002/slct.202102556openalex-snapshot
Chemical F/J‐Interconversion in the Prostaglandin Family: From Cloprostenol to Its Δ 12 ‐J 2 and 15‐Deoxy‐Δ 12,14 ‐J 2 Derivatives
inferred← citeshttps://doi.org/10.1002/slct.202401507openalex-snapshot
Synthesis of Electrophilic Cyclopent‐2‐enone Conjugates With Modulatory Effects on Inflammatory Responses Mediated by Nrf2/Keap1, NF‐κB and IL‐6
inferred← citeshttps://doi.org/10.1007/0-387-28500-8_7openalex-snapshot
Inflammation as a Mediator of Oxidative Stress and UPS Dysfunction
inferred← citeshttps://doi.org/10.1007/112_2014_18openalex-snapshot
The TRPA1 Channel in Inflammatory and Neuropathic Pain and Migraine
inferred← citeshttps://doi.org/10.1007/3418_020openalex-snapshot
The Pauson–Khand Reaction
inferred← citeshttps://doi.org/10.1007/978-1-4020-8399-0_3openalex-snapshot
Cellular and Environmental Electrophiles: Balancing Redox Signaling, Inflammation, and Cell Death Pathways
inferred← citeshttps://doi.org/10.1007/978-1-4419-9940-5_1openalex-snapshot
Metabolism and Roles of Eicosanoids in Brain
inferred← citeshttps://doi.org/10.1007/978-1-4471-4264-5_8openalex-snapshot
Mechanisms of the Acute Attack of Gout and Its Resolution
inferred← citeshttps://doi.org/10.1007/978-1-59745-364-6_15openalex-snapshot
In Vivo Models to Study Cyclooxygenase Products in Health and Disease: Introduction to Part III
inferred← citeshttps://doi.org/10.1007/978-1-60761-866-9_7openalex-snapshot
The Role of Inflammatory Mediators in Liver Failure
inferred← citeshttps://doi.org/10.1007/978-3-030-78315-0_19openalex-snapshot
Use of Nanotechnology to Improve 15d-PGJ2 Immunomodulatory Activities
inferred← citeshttps://doi.org/10.1007/978-3-319-04111-7_3openalex-snapshot
Contribution of Dietary Fat in Neuroinflammation
inferred← citeshttps://doi.org/10.1007/978-3-319-04111-7_7openalex-snapshot
Contribution of Dietary Fat in the Induction of Oxidative Stress
inferred← citeshttps://doi.org/10.1007/978-3-319-09943-9_4openalex-snapshot
Polyunsaturated Fatty Acid Oxygenated Metabolites in Skin
inferred← citeshttps://doi.org/10.1007/978-3-319-33889-7_2openalex-snapshot
Principles, Mechanisms of Action, and Future Prospects of Anti-inflammatory Drugs
inferred← citeshttps://doi.org/10.1007/978-3-319-41283-2_42openalex-snapshot
The Role of Selenoproteins in Resolution of Inflammation
inferred← citeshttps://doi.org/10.1007/978-3-642-29205-7_14openalex-snapshot
Genes Involved in the Thermal Tolerance of Livestock
inferred← citeshttps://doi.org/10.1007/978-4-431-55852-1_3openalex-snapshot
Regulation of HSF Activation and Repression
inferred← citeshttps://doi.org/10.1007/s00011-019-01231-1openalex-snapshot
Self-regulation of the inflammatory response by peroxisome proliferator-activated receptors
inferred← citeshttps://doi.org/10.1007/s00018-009-0039-xopenalex-snapshot
15-Deoxy-Δ12,14-prostaglandin-J2 reveals a new pVHL-independent, lysosomal-dependent mechanism of HIF-1α degradation
inferred← citeshttps://doi.org/10.1007/s00109-016-1384-5openalex-snapshot
15d-Prostaglandin J2 induced reactive oxygen species-mediated apoptosis during experimental visceral leishmaniasis
inferred← citeshttps://doi.org/10.1007/s00134-005-2596-2openalex-snapshot
The cyclopentenone prostaglandin 15-deoxyΔ12,14-prostaglandin J2 attenuates the development of zymosan-induced shock
inferred← citeshttps://doi.org/10.1007/s00214-005-0628-1openalex-snapshot
New designs for inhibitors of the NF-κB: DNA binding
inferred← citeshttps://doi.org/10.1007/s00424-006-0118-xopenalex-snapshot
Prostaglandin D2 and J2-series (PGJ2, Δ12-PGJ2) prostaglandins stimulate IL-6 and MCP-1, but inhibit leptin, expression and secretion by 3T3-L1 adipocytes
inferred← citeshttps://doi.org/10.1007/s00425-010-1265-zopenalex-snapshot
Salicylate-mediated suppression of jasmonate-responsive gene expression in Arabidopsis is targeted downstream of the jasmonate biosynthesis pathway
inferred← citeshttps://doi.org/10.1007/s00586-024-08550-wopenalex-snapshot
“Elucidating the immunomodulatory role of endocannabinoids in intervertebral disc degeneration”
inferred← citeshttps://doi.org/10.1007/s10067-018-4044-zopenalex-snapshot
Hypertrophic osteoarthropathy: estrogens, prostaglandinE2, prostaglandin A2, and the inflammatory reflex
inferred← citeshttps://doi.org/10.1007/s10452-021-09932-8openalex-snapshot
Lipid mediators in marine diatoms
inferred← citeshttps://doi.org/10.1007/s10549-006-9336-3openalex-snapshot
15-Deoxy-Δ12,14-prostaglandin J2 inhibits G2-M phase progression in human breast cancer cells via the down-regulation of cyclin B1 and survivin expression
inferred← citeshttps://doi.org/10.1007/s10555-018-9743-zopenalex-snapshot
Oxygenated lipid signaling in tumor-associated macrophages—focus on colon cancer
inferred← citeshttps://doi.org/10.1007/s10571-021-01104-4openalex-snapshot
Present State and Future Perspectives of Prostaglandins as a Differentiation Factor in Motor Neurons
inferred← citeshttps://doi.org/10.1007/s10787-020-00764-wopenalex-snapshot
Neuroinflammatory responses in Parkinson’s disease: relevance of Ibuprofen in therapeutics
inferred← citeshttps://doi.org/10.1007/s11011-025-01733-4openalex-snapshot
The role of arachidonic acid metabolites in major depressive disorder: mechanisms and therapeutic implications
inferred← citeshttps://doi.org/10.1007/s11064-006-9157-0openalex-snapshot
15-Deoxy-Δ12,14-prostaglandin J2 (15d-PGJ2) Induces Cell Death Through Caspase-independent Mechanism in A172 Human Glioma Cells
inferred← citeshttps://doi.org/10.1007/s11064-012-0781-6openalex-snapshot
Gemfibrozil, a Lipid Lowering Drug, Inhibits the Activation of Primary Human Microglia Via Peroxisome Proliferator-Activated Receptor β
inferred← citeshttps://doi.org/10.1007/s11101-017-9510-8openalex-snapshot
Metabolism of the plant hormone jasmonate: a sentinel for tissue damage and master regulator of stress response
inferred← citeshttps://doi.org/10.1007/s11172-023-4026-4openalex-snapshot
Some aspects of the synthesis and modification of cross-conjugated cyclopentenone prostaglandins
inferred← citeshttps://doi.org/10.1007/s11373-005-3009-9openalex-snapshot
Investigation of anticancer mechanism of clavulone II, a coral cyclopentenone prostaglandin analog, in human acute promyelocytic leukemia
inferred← citeshttps://doi.org/10.1007/s11373-005-4564-9openalex-snapshot
Biomedical Vignette
inferred← citeshttps://doi.org/10.1007/s12035-020-02174-zopenalex-snapshot
Prostaglandin A1 Decreases the Phosphorylation of Tau by Activating Protein Phosphatase 2A via a Michael Addition Mechanism at Cysteine 377
inferred← citeshttps://doi.org/10.1007/s12199-009-0128-3openalex-snapshot
“Combination-oriented molecular-targeting prevention” of cancer: a model involving the combination of TRAIL and a DR5 inducer
inferred← citeshttps://doi.org/10.1007/s12272-009-1320-0openalex-snapshot
Two enone fatty acids isolated from Gracilaria verrucosa suppress the production of inflammatory mediators by down-regulating NF-κB and STAT1 activity in lipopolysaccharide-stimulated RAW 264.7 cells
inferred← citeshttps://doi.org/10.1007/s13273-015-0050-2openalex-snapshot
PGA2-induced HO-1 attenuates G2M arrest by modulating GADD45α expression
inferred← citeshttps://doi.org/10.1007/s13273-017-0020-yopenalex-snapshot
PGA2 induces the expression of HO-1 by activating p53 in HCT116 cells
inferred← citeshttps://doi.org/10.1007/s13273-018-0043-zopenalex-snapshot
PGA2-induced expression of HO-1 is mediated by transcriptional upregulation of Nrf2
inferred← citeshttps://doi.org/10.1016/b978-0-12-373884-4.00072-0openalex-snapshot
Prostaglandins and Bone Metabolism
inferred← citeshttps://doi.org/10.1016/b978-0-12-396493-9.00004-2openalex-snapshot
Hematopoietic Prostaglandin D Synthase Inhibitors
inferred← citeshttps://doi.org/10.1016/b978-0-12-819404-1.00011-7openalex-snapshot
Fatty acid mediators and the inflammasome
inferred← citeshttps://doi.org/10.1016/b978-0-443-18866-4.00010-9openalex-snapshot
Host- and genomics-based antiviral approaches
inferred← citeshttps://doi.org/10.1016/b978-0-443-23763-8.00010-5openalex-snapshot
Modulation of enteric glial cells by nutraceuticals during pathological processes
inferred← citeshttps://doi.org/10.1016/b978-1-4160-3105-5.50013-xopenalex-snapshot
10.1016/b978-1-4160-3105-5.50013-x
inferred← citeshttps://doi.org/10.1016/b978-1-4160-6193-9.10013-2openalex-snapshot
Arachidonic Acid Metabolites and the Kidney
inferred← citeshttps://doi.org/10.1016/bs.abr.2021.09.004openalex-snapshot
The biosynthesis and metabolism of prostaglandins in microalgae
inferred← citeshttps://doi.org/10.1016/j.abb.2006.10.032openalex-snapshot
Direct evidence for the covalent modification of glutathione-S-transferase P1-1 by electrophilic prostaglandins: Implications for enzyme inactivation and cell survival
inferred← citeshttps://doi.org/10.1016/j.bbadis.2014.06.020openalex-snapshot
PACAP27 prevents Parkinson-like neuronal loss and motor deficits but not microglia activation induced by prostaglandin J2
inferred← citeshttps://doi.org/10.1016/j.bbadis.2017.03.017openalex-snapshot
Neurotoxic mechanisms by which the USP14 inhibitor IU1 depletes ubiquitinated proteins and Tau in rat cerebral cortical neurons: Relevance to Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.bbadis.2023.166924openalex-snapshot
Prostaglandin 15d-PGJ2 inhibits proliferation of lung adenocarcinoma cells by inducing ROS production and activation of apoptosis via sirtuin-1
inferred← citeshttps://doi.org/10.1016/j.bbalip.2007.02.014openalex-snapshot
n-3 and n-6 Polyunsaturated fatty acids induce the expression of COX-2 via PPARγ activation in human keratinocyte HaCaT cells
inferred← citeshttps://doi.org/10.1016/j.bbalip.2016.07.006openalex-snapshot
Cyclopentenone-containing oxidized phospholipids and their isoprostanes as pro-resolving mediators of inflammation
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2004.10.016openalex-snapshot
Prostaglandin D2 and J2 induce apoptosis in human leukemia cells via activation of the caspase 3 cascade and production of reactive oxygen species
inferred← citeshttps://doi.org/10.1016/j.bbrc.2004.04.095openalex-snapshot
Inverse correlation between jasmonic acid and salicylic acid during early wound response in rice
inferred← citeshttps://doi.org/10.1016/j.bbrc.2004.05.098openalex-snapshot
Δ12-Prostaglandin J2 inhibits the ubiquitin hydrolase UCH-L1 and elicits ubiquitin–protein aggregation without proteasome inhibition
inferred← citeshttps://doi.org/10.1016/j.bbrc.2005.03.040openalex-snapshot
Up-regulation of cyclooxygenase-2 expression by TSG-6 protein in macrophage cell line
inferred← citeshttps://doi.org/10.1016/j.bbrc.2005.07.130openalex-snapshot
Sequential induction of prostaglandin E and D synthases in inflammation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2005.12.196openalex-snapshot
Synthetic heteroprostanoids of A- and E-types as novel non-comprehensive inhibitors of adenylyl cyclase in rat hepatocytes
inferred← citeshttps://doi.org/10.1016/j.bbrc.2006.09.005openalex-snapshot
Addition of electrophilic lipids to actin alters filament structure
inferred← citeshttps://doi.org/10.1016/j.bbrc.2009.09.110openalex-snapshot
15-Deoxy-Δ12,14-prostaglandin J2 impairs the functions of histone acetyltransferases through their insolubilization in cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2012.01.046openalex-snapshot
High sodium butyrate levels induce MDR1 activation in colorectal cells: Impact of 15-deoxy-Δ12,14-prostaglandin J2 on the resistance to saquinavir
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.08.043openalex-snapshot
Peroxisome proliferator-activated receptors (PPARs) as therapeutic target in neurodegenerative disorders
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.04.040openalex-snapshot
Astrocytes synthesize primary and cyclopentenone prostaglandins that are negative regulators of their proliferation
inferred← citeshttps://doi.org/10.1016/j.bcp.2006.07.030openalex-snapshot
15-Deoxy-Δ12,14-prostaglandin J2 as a potential endogenous regulator of redox-sensitive transcription factors
inferred← citeshttps://doi.org/10.1016/j.bcp.2008.03.002openalex-snapshot
Atherosclerosis: A redox-sensitive lipid imbalance suppressible by cyclopentenone prostaglandins
inferred← citeshttps://doi.org/10.1016/j.bcp.2009.06.100openalex-snapshot
15-Deoxi-Δ12,14-prostaglandin J2 is a tubulin-binding agent that destabilizes microtubules and induces mitotic arrest
inferred← citeshttps://doi.org/10.1016/j.bcp.2011.07.089openalex-snapshot
Lycium barbarum (Goji Berry) extracts and its taurine component inhibit PPAR-γ-dependent gene transcription in human retinal pigment epithelial cells: Possible implications for diabetic retinopathy treatment
inferred← citeshttps://doi.org/10.1016/j.bcp.2011.07.100openalex-snapshot
15-Deoxy-Δ12,14-prostaglandin J2, an electrophilic lipid mediator of anti-inflammatory and pro-resolving signaling
inferred← citeshttps://doi.org/10.1016/j.bcp.2016.01.011openalex-snapshot
Activation of the MAPK/Akt/Nrf2-Egr1/HO-1-GCLc axis protects MG-63 osteosarcoma cells against 15d-PGJ2-mediated cell death
inferred← citeshttps://doi.org/10.1016/j.biocel.2009.12.013openalex-snapshot
Eicosanoids and the endogenous control of acute inflammatory resolution
inferred← citeshttps://doi.org/10.1016/j.biocel.2012.03.010openalex-snapshot
Long-term CFTR inhibition modulates 15d-prostaglandin J2 in human pulmonary cells
inferred← citeshttps://doi.org/10.1016/j.biortech.2019.03.147openalex-snapshot
Co-pyrolysis of phumdi and para grass biomass from Loktak Lake
inferred← citeshttps://doi.org/10.1016/j.bmc.2004.03.061openalex-snapshot
Reactions of some cyclopentenones with selected cysteine derivatives and biological activities of the product thioethers
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.10.038openalex-snapshot
Characterization of novel furan compounds on the basis of their radical scavenging activity and cytoprotective effects against glutamate- and lipopolysaccharide-induced insults
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.10.050openalex-snapshot
New jasmonate analogues as potential anti-inflammatory agents
inferred← citeshttps://doi.org/10.1016/j.bmc.2017.07.061openalex-snapshot
One-pot synthesis of bioactive cyclopentenones from α-linolenic acid and docosahexaenoic acid
inferred← citeshttps://doi.org/10.1016/j.bmcl.2005.06.025openalex-snapshot
Molecular recognition of 15-deoxy-Δ12,14-prostaglandin J2 by nuclear factor-kappa B and other cellular proteins
inferred← citeshttps://doi.org/10.1016/j.bmcl.2009.02.072openalex-snapshot
Selective, potent PPARγ agonists with cyclopentenone core structure
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.06.054openalex-snapshot
Prostaglandin phospholipid conjugates with unusual biophysical and cytotoxic properties
inferred← citeshttps://doi.org/10.1016/j.brainres.2005.01.046openalex-snapshot
Neuroprotective effects of prostaglandin A1 in animal models of focal ischemia
inferred← citeshttps://doi.org/10.1016/j.brainres.2009.07.059openalex-snapshot
Neuroprotective effects of (arylthio)cyclopentenone derivatives on manganese-induced apoptosis in PC12 cells
inferred← citeshttps://doi.org/10.1016/j.brainres.2009.08.015openalex-snapshot
(Arylthio)cyclopentenones derivatives prevent glutamate-induced HT22 cell death through a PPARγ-dependent pathway
inferred← citeshttps://doi.org/10.1016/j.brainres.2012.09.008openalex-snapshot
Neuroprotective cyclopentenone prostaglandins up-regulate neurotrophic factors in C6 glioma cells
inferred← citeshttps://doi.org/10.1016/j.brainresrev.2004.12.020openalex-snapshot
Hormone regulation of microglial cell activation: relevance to multiple sclerosis
inferred← citeshttps://doi.org/10.1016/j.canlet.2004.02.003openalex-snapshot
Targeting of epidermal growth factor receptor by cyclopentenone prostaglandin 15-Deoxy-Δ12,14-prostaglandin J2 in human oral squamous carcinoma cells
inferred← citeshttps://doi.org/10.1016/j.carres.2015.08.003openalex-snapshot
A common and versatile synthetic route to (−) and (+) pentenomycin I, (+) halopentenomycin I and dehydropentenomycin
inferred← citeshttps://doi.org/10.1016/j.cellsig.2007.06.004openalex-snapshot
Accumulation of hypoxia-inducible factor-1α through a novel electrophilic, thiol antioxidant-sensitive mechanism
inferred← citeshttps://doi.org/10.1016/j.cellsig.2011.08.002openalex-snapshot
A novel small molecule deubiquitinase inhibitor blocks Jak2 signaling through Jak2 ubiquitination
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.130833openalex-snapshot
Markers of lipid oxidation and inflammation in bronchial cells exposed to complete gasoline emissions and their organic extracts
inferred← citeshttps://doi.org/10.1016/j.chemphyslip.2003.09.016openalex-snapshot
The biochemistry of the isoprostane, neuroprostane, and isofuran pathways of lipid peroxidation
inferred← citeshttps://doi.org/10.1016/j.chemphyslip.2013.07.002openalex-snapshot
Biology and chemistry of neuroprostanes. First total synthesis of 17-A4-NeuroP: Validation of a convergent strategy to a number of cyclopentenone neuroprostanes
inferred← citeshttps://doi.org/10.1016/j.ddstr.2004.11.017openalex-snapshot
The endogenous control of acute inflammation – from onset to resolution
inferred← citeshttps://doi.org/10.1016/j.dyepig.2014.04.040openalex-snapshot
Synthesis and spectral properties of fluorescent photochromic diarylethenes with 6,6a-dihydropentalene-2(1H)-one ethene “bridge”
inferred← citeshttps://doi.org/10.1016/j.ejphar.2004.07.074openalex-snapshot
15d-prostaglandin J2 reduces multiple organ failure caused by wall-fragment of Gram-positive and Gram-negative bacteria
inferred← citeshttps://doi.org/10.1016/j.ejphar.2006.05.030openalex-snapshot
Induction of Fas clustering and apoptosis by coral prostanoid in human hormone-resistant prostate cancer cells
inferred← citeshttps://doi.org/10.1016/j.ejphar.2014.06.030openalex-snapshot
Reciprocal regulation of human platelet function by endogenous prostanoids and through multiple prostanoid receptors
inferred← citeshttps://doi.org/10.1016/j.exer.2004.10.009openalex-snapshot
Inhibition of corneal neovascularization by a peroxisome proliferator-activated receptor-γ ligand
inferred← citeshttps://doi.org/10.1016/j.exphem.2004.11.012openalex-snapshot
The cyclopentenone prostaglandin PGA2 costimulates the maturation of human dendritic cells
inferred← citeshttps://doi.org/10.1016/j.expneurol.2003.12.009openalex-snapshot
Neuroinflammation, COX-2, and ALS—a dual role?
inferred← citeshttps://doi.org/10.1016/j.febslet.2005.12.045openalex-snapshot
Adaptive response induced by lipid peroxidation products in cell cultures
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2011.05.063openalex-snapshot
The inhibitory effect of celecoxib and rosiglitazone on experimental endometriosis
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2007.03.009openalex-snapshot
Antiinflammatory effects of the cyclopentenone isoprostane 15-A2-IsoP in human gestational tissues
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2009.06.005openalex-snapshot
Select cyclopentenone prostaglandins trigger glutathione efflux and the role of ABCG2 transport
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2009.06.030openalex-snapshot
Regulation of Nrf2-dependent gene expression by 15-deoxy-Δ12,14-prostaglandin J2
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2010.12.039openalex-snapshot
15-Deoxy-Δ12,14-prostaglandin J2 induces Cox-2 expression in human osteosarcoma cells through MAPK and EGFR activation involving reactive oxygen species
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2011.12.016openalex-snapshot
15-Deoxy-Δ12,14-prostaglandin J2 modulates manganese-induced activation of the NF-κB, Nrf2, and PI3K pathways in astrocytes
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2021.03.002openalex-snapshot
Phytoprostanes and phytofurans modulate COX-2-linked inflammation markers in LPS-stimulated THP-1 monocytes by lipidomics workflow
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2023.08.019openalex-snapshot
Plasma oxylipin profiling by high resolution mass spectrometry reveal signatures of inflammation and hypermetabolism in amyotrophic lateral sclerosis
inferred← citeshttps://doi.org/10.1016/j.fsi.2023.108663openalex-snapshot
Comprehensive transcriptional and metabolomic analysis reveals the neuroprotective mechanism of dietary gamma-aminobutyric acid response to hypoxic stress in the Chinese mitten crab (Eriocheir sinensis)
inferred← citeshttps://doi.org/10.1016/j.gene.2006.05.026openalex-snapshot
Depot-specific prostaglandin synthesis in human adipose tissue: A novel possible mechanism of adipogenesis
inferred← citeshttps://doi.org/10.1016/j.ijcard.2014.03.086openalex-snapshot
15-deoxy-Δ12,14-PGJ2 promotes inflammation and apoptosis in cardiomyocytes via the DP2/MAPK/TNFα axis
inferred← citeshttps://doi.org/10.1016/j.ijcard.2014.09.111openalex-snapshot
Response to letter by Tsikas et al.
inferred← citeshttps://doi.org/10.1016/j.intimp.2006.02.013openalex-snapshot
Curcumin inhibits trinitrobenzene sulphonic acid-induced colitis in rats by activation of peroxisome proliferator-activated receptor gamma
inferred← citeshttps://doi.org/10.1016/j.isci.2019.100772openalex-snapshot
Clostridium butyricum Modulates the Microbiome to Protect Intestinal Barrier Function in Mice with Antibiotic-Induced Dysbiosis
inferred← citeshttps://doi.org/10.1016/j.jiec.2007.09.003openalex-snapshot
Continuous production of 1-methyl-1-cyclopenten-3-one using a micro module combined with tubular mixers
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2004.04.045openalex-snapshot
Transition metal-mediated routes to cyclopentenones
inferred← citeshttps://doi.org/10.1016/j.jprot.2011.03.028openalex-snapshot
Proteomic studies on protein modification by cyclopentenone prostaglandins: Expanding our view on electrophile actions
inferred← citeshttps://doi.org/10.1016/j.lab.2004.12.006openalex-snapshot
Insulin alters nuclear factor-κB and peroxisome proliferator-activated receptor-γ protein expression induced by glycated bovine serum albumin in vascular smooth-muscle cells
inferred← citeshttps://doi.org/10.1016/j.lfs.2009.04.010openalex-snapshot
The 15-Deoxy-Δ12,14-prostaglandin J2 inhibits LPS-stimulated AKT and NF-κB activation and suppresses interleukin-6 in osteoblast-like cells MC3T3E-1
inferred← citeshttps://doi.org/10.1016/j.mencom.2013.11.005openalex-snapshot
New α-methylidenecyclopentenone block from Corey lactone diol
inferred← citeshttps://doi.org/10.1016/j.mencom.2017.03.005openalex-snapshot
Side-modified 15-deoxy-Δ 12,14 -prostaglandin D 2 , precursor of corresponding PGJ 2 . Synthesis from cloprostenol and anticancer activity
inferred← citeshttps://doi.org/10.1016/j.mencom.2018.07.006openalex-snapshot
Synthetically attractive chiral cyclopentenone building blocks conjugated with tetrahydro- and 2-oxotetrahydrofurans
inferred← citeshttps://doi.org/10.1016/j.mencom.2019.07.003openalex-snapshot
Simple antitumor model compounds for cross-conjugated cyclopentenone prostaglandins
inferred← citeshttps://doi.org/10.1016/j.mencom.2020.01.003openalex-snapshot
A convenient synthesis of enantiopure (4aS,7aR)-1,4,4a,7a-tetrahydrocyclopenta[c]pyran-3,7-dione
inferred← citeshttps://doi.org/10.1016/j.mencom.2021.03.031openalex-snapshot
Formal synthesis of J-type prostaglandins based on enantiopure polyfunctional cyclopentenol derivative
inferred← citeshttps://doi.org/10.1016/j.mencom.2022.03.010openalex-snapshot
Cytotoxicity of novel cross-conjugated arylated cyclopentene-1,3-diones
inferred← citeshttps://doi.org/10.1016/j.mencom.2023.06.012openalex-snapshot
A facile synthesis of (±)-15-deoxy-Δ12,14-prostaglandin J2 methyl ester
inferred← citeshttps://doi.org/10.1016/j.mencom.2024.06.019openalex-snapshot
A concise synthesis of methyl dihydrojasmonate and methyl (5-methylidene-4-oxocyclopent-2-en-1-yl)acetate from D-glucose
inferred← citeshttps://doi.org/10.1016/j.mito.2006.12.005openalex-snapshot
Avicins, a novel plant-derived metabolite lowers energy metabolism in tumor cells by targeting the outer mitochondrial membrane
inferred← citeshttps://doi.org/10.1016/j.mito.2012.10.003openalex-snapshot
Role of mitochondria in programmed cell death mediated by arachidonic acid-derived eicosanoids
inferred← citeshttps://doi.org/10.1016/j.mvr.2004.11.004openalex-snapshot
The CNS pericyte response to low oxygen: early synthesis of cyclopentenone prostaglandins of the J-series
inferred← citeshttps://doi.org/10.1016/j.mvr.2005.01.007openalex-snapshot
Arachidonic acid cascade in endothelial pathobiology
inferred← citeshttps://doi.org/10.1016/j.neuint.2012.04.007openalex-snapshot
Daidzein has neuroprotective effects through ligand-binding-independent PPARγ activation
inferred← citeshttps://doi.org/10.1016/j.neuro.2008.08.003openalex-snapshot
Prevention of methylmercury-induced mitochondrial depolarization, glutathione depletion and cell death by 15-deoxy-delta-12,14-prostaglandin J2
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2005.04.030openalex-snapshot
Unusual astrocyte reactivity caused by the food mycotoxin ochratoxin A in aggregating rat brain cell cultures
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2006.09.029openalex-snapshot
The choroid plexus response to peripheral inflammatory stimulus
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2009.07.052openalex-snapshot
Activation of peripheral κ/δ opioid receptors mediates 15-deoxy-Δ12,14-prostaglandin J2 induced-antinociception in rat temporomandibular joint
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2021.09.001openalex-snapshot
Mutation of a Ubiquitin Carboxy Terminal Hydrolase L1 Lipid Binding Site Alleviates Cell Death, Axonal Injury, and Behavioral Deficits After Traumatic Brain Injury in Mice
inferred← citeshttps://doi.org/10.1016/j.pbi.2004.04.001openalex-snapshot
Archetype signals in plants: the phytoprostanes
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2013.04.006openalex-snapshot
Resolution of inflammation: Mechanisms and opportunity for drug development
inferred← citeshttps://doi.org/10.1016/j.phrs.2008.03.007openalex-snapshot
15-Deoxy-delta12,14-prostaglandin-J2 up-regulates cyclooxygenase-2 but inhibits prostaglandin-E2 production through a thiol antioxidant-sensitive mechanism
inferred← citeshttps://doi.org/10.1016/j.placenta.2005.11.009openalex-snapshot
15-Deoxy-Δ12,14-Prostaglandin J2 and Troglitazone Regulation of the Release of Phospholipid Metabolites, Inflammatory Cytokines and Proteases from Human Gestational Tissues
inferred← citeshttps://doi.org/10.1016/j.placenta.2006.05.011openalex-snapshot
The Role and Regulation of the Nuclear Factor Kappa B Signalling Pathway in Human Labour
inferred← citeshttps://doi.org/10.1016/j.plefa.2003.04.001openalex-snapshot
Phospholipase A2 isozymes in pregnancy and parturition
inferred← citeshttps://doi.org/10.1016/j.plefa.2003.04.005openalex-snapshot
Nuclear prostaglandin receptors: role in pregnancy and parturition?
inferred← citeshttps://doi.org/10.1016/j.plefa.2008.08.003openalex-snapshot
The effects of maternal dietary treatments with natural PPAR ligands on lipid metabolism in fetuses from control and diabetic rats
inferred← citeshttps://doi.org/10.1016/j.plefa.2009.11.007openalex-snapshot
Isoprostane nomenclature: Inherent problems may cause setbacks for the development of the isoprostanoid field
inferred← citeshttps://doi.org/10.1016/j.plefa.2012.03.009openalex-snapshot
Eicosanoids in skin inflammation
inferred← citeshttps://doi.org/10.1016/j.plefa.2017.06.010openalex-snapshot
Inhibition of indoleamine 2,3-dioxygenase activity by fatty acids and prostaglandins: A structure function analysis
inferred← citeshttps://doi.org/10.1016/j.plipres.2004.12.001openalex-snapshot
Advanced strategies in liposomal cancer therapy: Problems and prospects of active and tumor specific drug release
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2009.02.003openalex-snapshot
The mechanism of the rat liver cytochrome P4502E1 inhibition by the synthetic prostanoids of A-type
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2009.12.003openalex-snapshot
Prostaglandin A2 activates intrinsic apoptotic pathway by direct interaction with mitochondria in HL-60 cells
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2011.01.004openalex-snapshot
Induction of apoptosis by 15d-PGJ2 via ROS formation: An alternative pathway without PPARγ activation in non-small cell lung carcinoma A549 cells
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2014.02.001openalex-snapshot
15-Deoxy-Δ12,14-prostaglandin J2 induces PPARγ- and p53-independent apoptosis in rabbit synovial cells
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2019.03.001openalex-snapshot
Prostaglandin D2-ethanolamide induces skin cancer apoptosis by suppressing the activity of cellular antioxidants
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2020.106500openalex-snapshot
Activation of phospholipase A2 by prostaglandin in vitro
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