Publicacions en què col·labora amb ANDRÉS PARRA SÁNCHEZ (38)

2021

  1. Efficient in vitro and in vivo anti‐inflammatory activity of a diamine‐pegylated oleanolic acid derivative

    International Journal of Molecular Sciences, Vol. 22, Núm. 15

  2. Synthesis and Biological Activity of Triterpene-Coumarin Conjugates

    Journal of Natural Products, Vol. 84, Núm. 5, pp. 1587-1597

2019

  1. Maslinic acid conjugate with 7-amino-4-methylcoumarin as probe to monitor the temperature dependent conformational changes of human serum albumin by FRET

    Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, Vol. 214, pp. 161-169

  2. Oleanolic Acid Derivatives as Potential Inhibitors of HIV-1 Protease

    Journal of Natural Products, Vol. 82, Núm. 10, pp. 2886-2896

  3. Quantitative NMR analysis of L-Dopa in seeds from two varieties of Mucuna pruriens

    Phytochemical Analysis, Vol. 30, Núm. 1, pp. 89-94

2018

  1. Diamine and PEGylated-diamine conjugates of triterpenic acids as potential anticancer agents

    European Journal of Medicinal Chemistry, Vol. 148, pp. 325-336

  2. Semisynthesis of ω-Hydroxyalkylcarbonate Derivatives of Hydroxytyrosol as Antitrypanosome Agents

    Journal of Natural Products, Vol. 81, Núm. 9, pp. 2075-2082

2017

  1. Microwave-assisted extraction versus Soxhlet extraction to determine triterpene acids in olive skins

    Journal of Separation Science, Vol. 40, Núm. 5, pp. 1209-1217

  2. Synthesis and in vitro antiproliferative evaluation of PEGylated triterpene acids

    Fitoterapia, Vol. 120, pp. 25-40

2016

  1. Biotransformation of Salpichrolides A, C, and G by Three Filamentous Fungi

    Journal of Natural Products, Vol. 79, Núm. 6, pp. 1658-1667

  2. Semi-synthesis and antiproliferative evaluation of PEGylated pentacyclic triterpenes

    European Journal of Medicinal Chemistry, Vol. 118, pp. 64-78

  3. Synthesis and Antioxidant Activity of Hydroxytyrosol Alkyl-Carbonate Derivatives

    Journal of Natural Products, Vol. 79, Núm. 7, pp. 1737-1745

  4. The oleanolic acid derivative, 3-: O -succinyl-28- O -benzyl oleanolate, induces apoptosis in B16-F10 melanoma cells via the mitochondrial apoptotic pathway

    RSC Advances, Vol. 6, Núm. 96, pp. 93590-93601

2015

  1. Biotransformation of oleanolic and maslinic methyl esters by Rhizomucor miehei CECT 2749

    Phytochemistry, Vol. 117, pp. 500-508

  2. Effect of the solvent and the sample preparation on the determination of triterpene compounds in two-phase olive-mill-waste samples

    Journal of Agricultural and Food Chemistry, Vol. 63, Núm. 17, pp. 4269-4275

  3. Semi-synthesis of taraxerane triterpenoids from oleanolic acid

    Tetrahedron, Vol. 71, Núm. 5, pp. 792-800

2014

  1. Semi-synthesis of acylated triterpenes from olive-oil industry wastes for the development of anticancer and anti-HIV agents

    European Journal of Medicinal Chemistry, Vol. 74, pp. 278-301

  2. Solid-phase library synthesis of bi-functional derivatives of oleanolic and maslinic acids and their cytotoxicity on three cancer cell lines

    ACS Combinatorial Science, Vol. 16, Núm. 8, pp. 428-447

2013

  1. Biotransformation of oleanolic and maslinic acids by Rhizomucor miehei

    Phytochemistry, Vol. 94, pp. 229-237

  2. Enzymatic glycosylation of terpenoids

    Phytochemistry Reviews, Vol. 12, Núm. 2, pp. 327-339