Argitalpenak (52) ROSA MARIA DURAN PATRON argitalpenak

2024

  1. A Biomimetic Approach to Premyrsinane-Type Diterpenoids: Exploring Microbial Transformation to Enhance Their Chemical Diversity

    Plants, Vol. 13, Núm. 6

  2. Enhancing Structural Diversity of Lathyrane Derivatives through Biotransformation by the Marine-Derived Actinomycete Streptomyces puniceus BC-5GB.11

    International Journal of Molecular Sciences, Vol. 25, Núm. 4

2023

  1. Emericellopsis maritima and Purpureocillium lilacinum Marine Fungi as a Source of Functional Fractions with Antioxidant and Antitumor Potential in Colorectal Cancer: A Preliminary Study

    Journal of Marine Science and Engineering, Vol. 11, Núm. 10

  2. Marine-derived fungi as biocatalysts

    Frontiers in Microbiology, Vol. 14

  3. New Eremophilane-Type Sesquiterpenes from the Marine Sediment-Derived Fungus Emericellopsis maritima BC17 and Their Cytotoxic and Antimicrobial Activities

    Marine Drugs, Vol. 21, Núm. 12

2022

  1. Cryptic Metabolites from Marine-Derived Microorganisms Using OSMAC and Epigenetic Approaches

    Marine Drugs, Vol. 20, Núm. 2

  2. Editorial: Strategies for the Discovery of Fungal Natural Products

    Frontiers in Microbiology

  3. Erratum: Correction to "Phorbol Diesters and 12-Deoxy-16-hydroxyphorbol 13,16-Diesters Induce TGFα Release and Adult Mouse Neurogenesis" (Journal of medicinal chemistry (2021) 64 9 (6070-6084))

    Journal of medicinal chemistry

  4. Structural and biosynthetic studies of botrycinereic acid, a new cryptic metabolite from the fungus Botrytis cinerea

    Bioorganic Chemistry, Vol. 127

  5. The complemented mutant complΔBcstc7niaD, in the STC7 of Botrytis cinerea led to the characterization of 11,12,13-tri-nor-eremophilenols derivatives

    Phytochemistry, Vol. 193

2021

  1. Phorbol Diesters and 12-Deoxy-16-hydroxyphorbol 13,16-Diesters Induce TGFα Release and Adult Mouse Neurogenesis

    Journal of Medicinal Chemistry, Vol. 64, Núm. 9, pp. 6070-6084

  2. Synthesis, fungitoxic activity against botrytis cinerea and phytotoxicity of alkoxyclovanols and alkoxyisocaryolanols

    Journal of Fungi, Vol. 7, Núm. 12

2019

  1. Lathyrane, Premyrsinane, and Related Diterpenes from Euphorbia boetica: Effect on in Vitro Neural Progenitor Cell Proliferation

    Journal of Natural Products, Vol. 82, Núm. 9, pp. 2517-2528

  2. The current status on secondary metabolites produced by plant pathogenic Colletotrichum species

    Phytochemistry Reviews, Vol. 18, Núm. 1, pp. 215-239

2018

  1. Isotopic Labeling Studies Reveal the Patulin Detoxification Pathway by the Biocontrol Yeast Rhodotorula kratochvilovae LS11

    Journal of Natural Products, Vol. 81, Núm. 12, pp. 2692-2699

  2. Structural and biosynthetic studies on eremophilenols related to the phytoalexin capsidiol, produced by Botrytis cinerea

    Phytochemistry, Vol. 154, pp. 10-18

2016

  1. Chemically Induced Cryptic Sesquiterpenoids and Expression of Sesquiterpene Cyclases in Botrytis cinerea Revealed New Sporogenic (+)-4-Epieremophil-9-en-11-ols

    ACS Chemical Biology, Vol. 11, Núm. 5, pp. 1391-1400

2013

  1. A Shared Biosynthetic Pathway for Botcinins and Botrylactones Revealed through Gene Deletions

    ChemBioChem, Vol. 14, Núm. 1, pp. 132-136

  2. Phytotoxic activity and metabolism of Botrytis cinerea and structure-activity relationships of isocaryolane derivatives

    Journal of Natural Products, Vol. 76, Núm. 6, pp. 1016-1024

  3. Searching for genes responsible for patulin degradation in a biocontrol yeast provides insight into the basis for resistance to this mycotoxin

    Applied and Environmental Microbiology, Vol. 79, Núm. 9, pp. 3101-3115