Publikationen, an denen er mitarbeitet ANDRÉS PARRA SÁNCHEZ (12)

2023

  1. Synthesis, Optical Properties, and Antiproliferative Evaluation of NBD-Triterpene Fluorescent Probes

    Journal of Natural Products, Vol. 86, Núm. 1, pp. 166-175

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

2020

  1. A diamine-pegylated oleanolic acid derivative induced efficient apoptosis through a death receptor and mitochondrial apoptotic pathway in hepg2 human hepatoma cells

    Biomolecules, Vol. 10, Núm. 10, pp. 1-22

2019

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

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

2018

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

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

2017

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

    Fitoterapia, Vol. 120, pp. 25-40

2016

  1. Maslinic acid, a natural triterpene, induces a death receptor-mediated apoptotic mechanism in caco-2 p53-deficient colon adenocarcinoma cells

    PLoS ONE, Vol. 11, Núm. 1

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

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

  3. 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

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