Search Results - "PayÁ, Miguel"
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Pharmacological Interventions to Ameliorate Neuropathological Symptoms in a Mouse Model of Lafora Disease
Published in Molecular neurobiology (01-03-2016)“…Lafora disease (LD, OMIM 254780) is a rare fatal neurodegenerative disorder that usually occurs during childhood with generalized tonic-clonic seizures,…”
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NF-κB and STAT3 Inhibition as a Therapeutic Strategy in Psoriasis: In Vitro and In Vivo Effects of BTH
Published in Journal of investigative dermatology (01-10-2013)“…Benzo[b]thiophen-2-yl-3-bromo-5-hydroxy-5H-furan-2-one (BTH) is a simple and interesting synthetic derivative of petrosaspongiolide M, a natural compound…”
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3
Defective Induction of COX-2 Expression by Psoriatic Fibroblasts Promotes Pro-inflammatory Activation of Macrophages
Published in Frontiers in immunology (20-03-2019)“…Fibroblasts play an important role as members of the innate immune system through the secretion of COX-2-derived inflammatory mediators such as prostaglandin E…”
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Adenosine A2A and A2B Receptors Differentially Modulate Keratinocyte Proliferation: Possible Deregulation in Psoriatic Epidermis
Published in Journal of investigative dermatology (01-01-2017)“…Adenosine is a potent regulator of inflammation and immunity, but the role of adenosine receptors in keratinocytes remains controversial. We determined that in…”
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Anti-inflammatory and analgesic activity of a novel inhibitor of microsomal prostaglandin E synthase-1 expression
Published in European journal of pharmacology (12-10-2009)“…In a previous study, we reported a new γ-hydroxybutenolide derivative, 4-benzo[ b]thiophen-2-yl-3-bromo-5-hydroxy-5 H-furan-2-one (BTH), as inhibitor of…”
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6
Perthamides C–F, potent human antipsoriatic cyclopeptides
Published in Tetrahedron (07-10-2011)“…Two new cyclopeptides, perthamides E and F were isolated from the polar extracts of the sponge Theonella swinhoei. The new structures, featuring an…”
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Avarol inhibits TNF-α generation and NF-κB activation in human cells and in animal models
Published in Life sciences (1973) (30-01-2008)“…Avarol is a marine sesquiterpenoid hydroquinone with interesting pharmacological properties including anti-inflammatory and antipsoriatic effects. In the…”
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The synthesis and effect of fluorinated chalcone derivatives on nitric oxide production
Published in Bioorganic & medicinal chemistry letters (05-08-2002)“…Dimethoxy- and trimethoxychalcone derivatives, with various patterns of fluorination, were synthesized and evaluated for their influence on nitric oxide…”
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Potential antipsoriatic effect of chondroitin sulfate through inhibition of NF-κB and STAT3 in human keratinocytes
Published in Pharmacological research (01-04-2013)“…Chondroitin sulfate (CS) is a natural glycosaminoglycan, formed by the 1–3 linkage of d-glucuronic acid to N-acetylgalactosamine, present in the extracellular…”
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10
Anthrax lethal toxin down-regulates type-IIA secreted phospholipase A2 expression through MAPK/NF-κB inactivation
Published in Biochemical pharmacology (01-04-2010)Get full text
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Coscinolactams A and B : new nitrogen-containing sesterterpenoids from the marine sponge Coscinoderma mathewsi exerting anti-inflammatory properties
Published in Tetrahedron (11-04-2009)Get full text
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Synthesis and inhibitory activity of dimethylamino-chalcone derivatives on the induction of nitric oxide synthase
Published in European journal of medicinal chemistry (01-08-2002)“…A series of nine dimethylamino-chalcone derivatives (1,3-diaryl-propenones) was synthesized and screened as potential inhibitors of NO and PGE 2 production in…”
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Identification of avarol derivatives as potential antipsoriatic drugs using an in vitro model for keratinocyte growth and differentiation
Published in Life sciences (1973) (17-11-2006)“…Avarol, a marine sesquiterpenoid hydroquinone, and 14 avarol derivatives have shown interesting anti-inflammatory properties in previous studies. In this…”
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Protection against 2,4,6-trinitrobenzenesulphonic acid-induced colonic inflammation in mice by the marine products bolinaquinone and petrosaspongiolide M
Published in Biochemical pharmacology (15-05-2005)“…Proinflammatory mediators, namely eicosanoids, reactive oxygen and nitrogen species and cytokines, are clearly involved in the pathogenesis of intestinal bowel…”
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Modulatory effect of bolinaquinone, a marine sesquiterpenoid, on acute and chronic inflammatory processes
Published in The Journal of pharmacology and experimental therapeutics (01-03-2003)“…The marine metabolite bolinaquinone is a novel inhibitor of secretory phospholipase A(2) (sPLA(2)), with a potency on the human synovial enzyme (group II)…”
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Synthesis and evaluation of diverse thio avarol derivatives as potential UVB photoprotective candidates
Published in Bioorganic & medicinal chemistry letters (01-05-2007)“…Semisynthesis of 13 new thio avarol derivatives ( 4– 16) and in vitro evaluation on the photodamage response induced by UVB irradiation are described. Their…”
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Potential Antipsoriatic Avarol Derivatives as Antioxidants and Inhibitors of PGE2 Generation and Proliferation in the HaCaT Cell Line
Published in Journal of natural products (Washington, D.C.) (24-09-2004)“…The synthesis and structure−activity relationships for a series of 14 new avarol derivatives as antioxidants and inhibitors of cell proliferation and PGE2…”
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Cacospongionolide B suppresses the expression of inflammatory enzymes and tumour necrosis factor‐α by inhibiting nuclear factor‐κB activation
Published in British journal of pharmacology (01-04-2003)“…The marine product cacospongionolide B, a sesterterpene isolated from the Mediterranean sponge Fasciospongia cavernosa, is an inhibitor of secretory…”
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Inhibition of the NF-κB signaling pathway mediates the anti-inflammatory effects of petrosaspongiolide M
Published in Biochemical pharmacology (01-03-2003)“…Petrosaspongiolide M (PT) is a potent secretory phospholipase A 2 inhibitor and anti-inflammatory agent. This marine metabolite reduced the production of…”
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Modulation of acute and chronic inflammatory processes by cacospongionolide B, a novel inhibitor of human synovial phospholipase A2
Published in British journal of pharmacology (01-01-1999)“…Cacospongionolide B is a novel marine metabolite isolated from the sponge Fasciospongia cavernosa. In in vitro studies, this compound inhibited phospholipase…”
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