Zobrazeno 1 - 10 of 164 pro vyhledávání: '"Cabedo N"'
1
Akademický článek
Estudio de la prevalencia y la caracterización del dolor postoperatorio inmediato en la Unidad de Recuperación Postanestésica
Autor: Cabedo, N., Valero, R., Alcón, A., Gomar, C.
Publikováno v: In Revista Española de Anestesiología y Reanimación August-September 2017 64(7):375-383
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2
Akademický článek
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3
Synthesis and biological studies of 'Polycerasoidol' and 'trans-delta-Tocotrienolic acid' derivatives as PPARalpha and/or PPARgamma agonists
Autor: Vila L, Cabedo N, Villarroel-Vicente C, Garcia A, Bernabeu A, Hennuyer N, Staels B, Franck X, Figadere B, Sanz M, Cortes D
Publikováno v: BIOORGANIC & MEDICINAL CHEMISTRY
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
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2-Prenylated benzopyrans represent a class of natural and synthetic compounds showing a wide range of significant activities. Polycerasoidol is a natural prenylated benzopyran isolated from the stem bark of Polyalthia cerasoides (Annonaceae) that exh
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::ac87c3127028e7557434237629aec988
https://www.fundanet.incliva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=16333
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4
Synthesis of 2-Prenylated Alkoxylated Benzopyrans by Horner- Wadsworth-Emmons Olefination with PPAR alpha/gamma Agonist Activity
Autor: Garcia A, Vila L, Marin P, Bernabeu A, Villarroel-Vicente C, Hennuyer N, Staels B, Franck X, Figadere B, Cabedo N, Cortes D
Publikováno v: ACS Medicinal Chemistry Letters
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
We have synthesized series of 2-prenylated benzopyrans as analogues of the natural polycerasoidol, a dual PPAR alpha/gamma agonist with anti-inflammatory effects. The prenylated side chain consists of five or nine carbons with an alpha-alkoxy-alpha,b
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::0cc7b35bc770fcdc838f10cf320b07c1
https://www.fundanet.incliva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=16360
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5
Natural products and analogs as preventive agents for metabolic syndrome via peroxisome proliferator-activated receptors: An overview
Autor: Villarroel-Vicente C, Gutierrez-Palomo S, Ferri J, Cortes D, Cabedo N
Publikováno v: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
Natural products and synthetic analogs have drawn much attention as potential therapeutical drugs to treat metabolic syndrome. We reviewed the underlying mechanisms of 32 natural products and analogs with potential pharmacological effects invitro, an
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::aedcb9c43dc2b5ddff1d0a1bbbb4f675
https://www.fundanet.incliva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=15767
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6
1-(2 '-Bromobenzyl)-6,7-dihydroxy-N-methyl-tetrahydroisoquinoline and 1,2-Demethyl-nuciferine as Agonists in Human D-2 Dopamine Receptors
Autor: Silva A, Vila L, Marques P, Moreno L, Loza M, Sanz M, Cortes D, Castro M, Cabedo N
Publikováno v: JOURNAL OF NATURAL PRODUCTS
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
Certain D-2-like dopamine receptor (DR) agonists are useful therapeutically as antiparkinsonian drugs, whereas D-2-like DR antagonists or partial agonists are proven effective as antipsychotics. Two isoquinoline derivatives, 1-(2'-bromobenzy1)-6,7-di
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::e31006c08fa2d5f409a9ab201a3b13e2
https://www.fundanet.incliva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=4370
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7
Akademický článek
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9
Synthesis and biological evaluation of sphingosine kinase 2 inhibitors with anti-inflammatory activity
Autor: Vettorazzi M, Vila L, Lima S, Acosta L, Yepes F, Palma A, Cobo J, Tengler J, Malik I, Alvarez S, Marques P, Cabedo N, Sanz M, Jampilek J, Spiegel S, Enriz R
Publikováno v: ARCHIV DER PHARMAZIE
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
The synthesis of inhibitors of SphK2 with novel structural scaffolds is reported. These compounds were designed from a molecular modeling study, in which the molecular interactions stabilizing the different complexes were taken into account. Particul
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::d50d4e1aa0fb67ee3da947e0edab1e11
https://www.fundanet.incliva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=2867
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