Faustino Mollinedo García-rekin lankidetzan egindako argitalpenak (29)

2021

  1. Methylsulfanylpyridine based diheteroaryl isocombretastatin analogs as potent anti-proliferative agents

    European Journal of Medicinal Chemistry, Vol. 209

  2. New indolesulfonamide derivatives targeting the colchicine site of tubulin: synthesis, anti-tumour activity, structure–activity relationships, and molecular modelling

    Journal of Enzyme Inhibition and Medicinal Chemistry, Vol. 36, Núm. 1, pp. 2025-2044

2020

  1. Potent colchicine-site ligands with improved intrinsic solubility by replacement of the 3,4,5-trimethoxyphenyl ring with a 2-methylsulfanyl-6-methoxypyridine ring

    Bioorganic Chemistry, Vol. 98

2016

  1. C-Geranylated flavonoids from Paulownia tomentosa fruits with antimicrobial potential and synergistic activity with antibiotics

    Pharmaceutical Biology, Vol. 54, Núm. 8, pp. 1398-1407

  2. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

    Autophagy, Vol. 12, Núm. 1, pp. 1-222

  3. The alkylphospholipid edelfosine shows activity against Strongyloides venezuelensis and induces apoptosis-like cell death

    Acta Tropica, Vol. 162, pp. 180-187

2015

  1. Eficacia de alquil-fosfolípidos frente a Strongyloides venezuelensis

    XIX Congreso de la Sociedad Española de Parasitología (SOCEPA)

  2. Erratum: In Vitro and in Vivo Anti-Schistosomal Activity of the Alkylphospholipid Analog Edelfosine (PLoS ONE (2014) 9:10 (e109431) DOI: 10.1371/journal.pone.0109431)

    PLoS ONE

  3. Inhibition of granulomatous inflammation and prophylactic treatment of schistosomiasis with a combination of edelfosine and Praziquantel

    PLoS Neglected Tropical Diseases, Vol. 9, Núm. 7

2014

  1. In vitro and in vivo anti-schistosomal activity of the alkylphospholipid analog edelfosine

    PLoS ONE, Vol. 9, Núm. 10

  2. The HSP90 inhibitor 17-AAG potentiates the antileishmanial activity of the ether lipid edelfosine

    Acta Tropica, Vol. 131, Núm. 1, pp. 32-36

2013

  1. Endowing indole-based tubulin inhibitors with an anchor for derivatization: Highly potent 3-substituted indolephenstatins and indoleisocombretastatins

    Journal of Medicinal Chemistry, Vol. 56, Núm. 7, pp. 2813-2827

  2. Synthesis and evaluation as antitumor agents of 1,4-naphthohydroquinone derivatives conjugated with amino acids and purines

    Archiv der Pharmazie, Vol. 346, Núm. 12, pp. 882-890

2012

  1. Apoptotic mechanisms are involved in the death of Strongyloides venezuelensis after triggering of nitric oxide

    Parasite Immunology, Vol. 34, Núm. 12, pp. 570-580

  2. Guidelines for the use and interpretation of assays for monitoring autophagy

    Autophagy, Vol. 8, Núm. 4, pp. 445-544

  3. In vitro and in vivo efficacy of ether lipid edelfosine against Leishmania spp. and SbV-resistant parasites

    PLoS Neglected Tropical Diseases, Vol. 6, Núm. 4

  4. Lignopurines: A new family of hybrids between cyclolignans and purines. Synthesis and biological evaluation

    European Journal of Medicinal Chemistry, Vol. 58, pp. 377-389

2010

  1. Synthesis and biological evaluation of new podophyllic aldehyde derivatives with cytotoxic and apoptosis-inducing activities

    Journal of Medicinal Chemistry, Vol. 53, Núm. 3, pp. 983-993

2009

  1. Isocombretastatins A: 1,1-Diarylethenes as potent inhibitors of tubulin polymerization and cytotoxic compounds

    Bioorganic and Medicinal Chemistry, Vol. 17, Núm. 17, pp. 6422-6431

2008

  1. Aplidin, a marine organism-derived compound with potent antimyeloma activity in vitro and in vivo

    Cancer Research, Vol. 68, Núm. 13, pp. 5216-5225