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Challenging core-shell stationary phases with the separation of closely related anti-cancer compounds: performance studies and application to drug quantitation in cell cultures with multi-well plate clean-up

Autor: González-Ruiz, Víctor, Olives, Ana I., Martín, M. Antonia

Publikováno v: In Journal of Chromatography A 17 October 2014 1364:83-95

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Influence of the presence of methyl cyclodextrins in high-performance liquid chromatography mobile phases on the separation of β-carboline alkaloids

Autor: León, Andrés G., Olives, Ana I., del Castillo, Benito, Martín, M. Antonia

Publikováno v: In Journal of Chromatography A 2008 1192(2):254-258

Correction to Tetrahydroisoquinoline-Derived Urea and 2,5-Diketopiperazine Derivatives as Selective Antagonists of the Transient Receptor Potential Melastatin 8 (TRPM8) Channel Receptor and Antiprostate Cancer Agents (vol 59, pg 5661, 2016)

Autor: De Petrocellis, Luciano, Arroyo, Francisco J., Orlando, Pierangelo, Moriello, Aniello Schiano, Vitale, Rosa Maria, Amodeo, Pietro, Sanchez, Aranzazu, Roncero, Cesareo, Bianchini, Giulia, Martin, M. Antonia, Lopez-Alvarado, Pilar, Menendez, J. Carlos

Publikováno v: Journal of medicinal chemistry 59 (2016): 7697–7697. doi:10.1021/acs.jmedchem.6b01091
info:cnr-pdr/source/autori:De Petrocellis, Luciano; Arroyo, Francisco J.; Orlando, Pierangelo; Moriello, Aniello Schiano; Vitale, Rosa Maria; Amodeo, Pietro; Sanchez, Aranzazu; Roncero, Cesareo; Bianchini, Giulia; Martin, M. Antonia; Lopez-Alvarado, Pilar; Menendez, J. Carlos/titolo:Correction to Tetrahydroisoquinoline-Derived Urea and 2,5-Diketopiperazine Derivatives as Selective Antagonists of the Transient Receptor Potential Melastatin 8 (TRPM8) Channel Receptor and Antiprostate Cancer Agents (vol 59, pg 5661, 2016)/doi:10.1021%2Facs.jmedchem.6b01091/rivista:Journal of medicinal chemistry/anno:2016/pagina_da:7697/pagina_a:7697/intervallo_pagine:7697–7697/volume:59

Tetrahydroisoquinoline derivatives containing embedded urea functions were identified as selective TRPM8 channel receptor antagonists. Structure-activity relationships were investigated, with the following conclusions: (a) The urea function and the t

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