Mostrando 10 resultados de: 64
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scopus(64)
Highly Fluorescent Green Fluorescent Protein Chromophore Analogues Made by Decorating the Imidazolone Ring
ArticleAbstract: The synthesis and photophysical behavior of an unexplored family of green fluorescent protein (GFP)-Palabras claves:cell staining, Fluorescence, imidazolone derivatives, proteins, TD-DFT calculationsAutores:Antonio Salgado, Domingo A., Gutiérrez S., Martínez-Lõpez D., Morón M., Sampedro D., Sucunza D., Vaquero J.J.Fuentes:scopusElectrosynthesis of Oxazol-2(3H)-Ones and Diaroylhydrazines from 1,2-Dicarbonyl Compounds and Arenediazonium Salts
ArticleAbstract: New five-membered oxazol-2(3H)-one heterocycles and 1,2-diaroylhydrazines are obtained in good yieldPalabras claves:1,2-diaroylhydrazines, 3-methyl-oxazol-2(3H)-ones, electrochemical reduction, N-methylformamide, radical couplingAutores:Antonio Salgado, Barba F., Batanero B., Quirós I.Fuentes:scopusEnantiomeric separation of ivabradine by cyclodextrin-electrokinetic chromatography. Effect of amino acid chiral ionic liquids
ArticleAbstract: A chiral methodology was developed for the first time to ensure the quality control of ivabradine, aPalabras claves:capillary electrophoresis, Chiral ionic liquids, chromatography, cyclodextrins, Electrokinetic, Enantioseparation, IvabradineAutores:Antonio Salgado, Casado N., Castro-Puyana M., García M.Á., Marina M.L.Fuentes:scopusEnantiomeric separation of the antiuremic drug colchicine by electrokinetic chromatography. Method development and quantitative analysis
ArticleAbstract: Two analytical methodologies were developed by CE enabling the enantiomeric separation of colchicinePalabras claves:capillary electrophoresis, colchicine, enantiomer migration order, Enantioseparation, H NMR, QuantitationAutores:Antonio Salgado, Castro-Puyana M., García M.Á., Marina M.L., Menéndez-López N., Valimaña-Traverso J.Fuentes:scopusFormation, Characterization, and Occurrence of β-Carboline Alkaloids Derived from α-Dicarbonyl Compounds and l -Tryptophan
ArticleAbstract: β-Carbolines (βCs) are naturally occurring bioactive alkaloids, whereas α-dicarbonyl compounds are rPalabras claves:3-deoxyglucosone, advanced glycation, glyoxal, Maillard reaction, methylglyoxal, tryptophan, α-dicarbonyl-derived βCs, α-dicarbonyls, β-carboline alkaloidsAutores:Antonio Salgado, Herraiz M., Herraiz T., Mateo H., Peña A.Fuentes:scopusFragment-Hopping-Based Discovery of a Novel Chemical Series of Proto-Oncogene PIM-1 Kinase Inhibitors
ArticleAbstract: A new chemical series, triazolo[4,5-b]pyridines, has been identified as an inhibitor of PIM-1 by a cPalabras claves:Autores:Albarran M.I., Alvarez R.M., Antonio Salgado, Bischoff J.R., Blanco C., Kurz G., Ortega M.A., Oyarzabal J., Pastor J., Pevarello P., Rabal O., Saluste G.Fuentes:scopusC-H Functionalization of BN-Aromatics Promoted by Addition of Organolithium Compounds to the Boron Atom
ArticleAbstract: Addition of an organolithium compound to a BN-phenanthrene with embedded B and N atoms is proposed tPalabras claves:Autores:Abengózar A., Antonio Salgado, Fernández-González M., Frutos L., García-García P., Sucunza D., Vaquero J.J.Fuentes:scopusDetermination of the structure of a hybrid between 2-(1,4-benzoquinone) acetic acid and a linear peptide by electrospray ionization mass spectrometry [1]
OtherAbstract:Palabras claves:Autores:Antonio Salgado, Blázquez J.Fuentes:scopusDifferentiation between [1,2,4]triazolo[1,5-a] pyrimidine and [1,2,4]triazolo[4,3-a]- Pyrimidine regioisomers by <sup>1</sup>H-<sup>15</sup>N HMBC experiments
ArticleAbstract: The condensation of malonoaldehyde derivatives with either a 3-amino-[1,2,4]-triazole or a 3,5-diamiPalabras claves:1 H, 13 C, 15 N, HMBC, Isomerisation, NMR, Regioisomerism, [1,2,4]triazolo[1,5-a] pyrimidines, [1,2,4]triazolo[4,3-a]pyrimidinesAutores:Antonio Salgado, Collazo A., Pevarello P., Varela C.Fuentes:scopusDiscovery of mitogen-activated protein kinase-interacting kinase 1 inhibitors by a comprehensive fragment-oriented virtual screening approach
ArticleAbstract: Mitogen-activated protein kinase-interacting kinases 1 and 2 (MNK1 and MNK2) phosphorylate the oncogPalabras claves:Autores:Albarran M.I., Antonio Salgado, Bischoff J.R., Corrionero A., Fominaya J., Mateos G., Oyarzabal J., Palacios I., Pastor J., Rabal O., Reymundo I., Urbano-Cuadrado M., Zarich N.Fuentes:scopus