Works about POLYKETIDES
Results: 1612
In vitro effect of polar extracts from Annona glabra seeds on Fusarium solani.
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- Revista Caatinga, 2024, v. 37, p. 1, doi. 10.1590/1983-21252024v3711810rc
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- Article
Active ingredient of graviola embedded in textiles: Sächsisches Textilforschungs-institut e.V. (STFI) Chemnitz/Germany.
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- Melliand International / Melliand Textilberichte, 2024, n. 6, p. 43
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- Article
Synthesis of Annonacin Isolated from Annona densicoma.
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- Bioscience, Biotechnology & Biochemistry, 2010, v. 74, n. 6, p. 1274, doi. 10.1271/bbb.90902
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Extensive Mutational Analysis of Modular-Iterative Mixed Polyketide Biosynthesis of Lankacidin in Streptomyces rochei.
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- Bioscience, Biotechnology & Biochemistry, 2009, v. 73, n. 12, p. 2712, doi. 10.1271/bbb.90591
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Biosynthesis of Resorcylic Acid Lactone (5S)-5-Hydroxylasiodiplodin in Lasiodiplodia theobromae.
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- Bioscience, Biotechnology & Biochemistry, 2009, v. 73, n. 11, p. 2522, doi. 10.1271/bbb.90417
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Synthesis of Annonaceous Acetogenins from Muricatacin.
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- Bioscience, Biotechnology & Biochemistry, 2007, v. 71, n. 10, p. 2367, doi. 10.1271/bbb.70202
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Biosynthetic Origin of the Carbon Skeleton and Nitrogen Atom of Pamamycin-607, a Nitrogen-Containing Polyketide.
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- Bioscience, Biotechnology & Biochemistry, 2005, v. 69, n. 2, p. 315, doi. 10.1271/bbb.69.315
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Structural Revision of Epoxyrollins A and B, Biosynthetic Precursors of Annonaceous Acetogenins.
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- Bioscience, Biotechnology & Biochemistry, 2003, v. 67, n. 6, p. 1438, doi. 10.1271/bbb.67.1438
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Isolation, Structure Elucidation, and Biological Activity of the Selective TACR2 Antagonist Tumonolide and its Aldehyde from a Marine Cyanobacterium.
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- Chemistry - A European Journal, 2024, v. 30, n. 50, p. 1, doi. 10.1002/chem.202401393
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An Efficient and Scalable "Second Generation" Total Synthesis of the Marine Polyketide Limaol Endowed with Antiparasitic Activity.
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- Chemistry - A European Journal, 2024, v. 30, n. 40, p. 1, doi. 10.1002/chem.202401429
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Advances Toward Amphidinolides C, F and U: Isolations, Synthetic Studies and Total Syntheses.
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- Chemistry - A European Journal, 2024, v. 30, n. 27, p. 1, doi. 10.1002/chem.202400471
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Reductive Release from a Hybrid PKS‐NRPS during the Biosynthesis of Pyrichalasin H.
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- Chemistry - A European Journal, 2024, v. 30, n. 4, p. 1, doi. 10.1002/chem.202302590
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A Common C<sub>2</sub>‐Symmetric 2,2'‐Biphenol Building Block and its Application in the Synthesis of (+)‐di‐epi‐Gonytolide A.
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- Chemistry - A European Journal, 2023, v. 29, n. 34, p. 1, doi. 10.1002/chem.202300941
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Modifications of Acyl Carrier Protein‐Bound Glycosylated Polyketides in Pactamycin Biosynthesis.
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- Chemistry - A European Journal, 2023, v. 29, n. 33, p. 1, doi. 10.1002/chem.202301056
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Unprecedented Combination of Polyketide Natural Product Fragments Identifies the New Hedgehog Signaling Pathway Inhibitor Grismonone.
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- Chemistry - A European Journal, 2022, v. 28, n. 67, p. 1, doi. 10.1002/chem.202202164
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Scalable Total Synthesis of Acremolactone B.
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- Angewandte Chemie, 2024, v. 136, n. 29, p. 1, doi. 10.1002/ange.202314800
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Enantioselective Synthesis of the 1,3‐Dienyl‐5‐Alkyl‐6‐Oxy Motif: Method Development and Total Synthesis.
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- Angewandte Chemie, 2024, v. 136, n. 15, p. 1, doi. 10.1002/ange.202400478
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Methylene C(sp<sup>3</sup>)−H Arylation Enables the Stereoselective Synthesis and Structure Revision of Indidene Natural Products.
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- Angewandte Chemie, 2024, v. 136, n. 1, p. 1, doi. 10.1002/ange.202316103
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Stereospecific Conversion of Boronic Esters into Enones using Methoxyallene: Application in the Total Synthesis of 10‐Deoxymethynolide.
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- Angewandte Chemie, 2023, v. 135, n. 50, p. 1, doi. 10.1002/ange.202312054
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Chemoenzymatic Synthesis of Cylindrocyclophanes A and F and Merocyclophanes A and D.
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- Angewandte Chemie, 2023, v. 135, n. 46, p. 1, doi. 10.1002/ange.202307602
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Modular Oxime Formation by a trans‐AT Polyketide Synthase.
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- Angewandte Chemie, 2023, v. 135, n. 34, p. 1, doi. 10.1002/ange.202304481
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Somalactams A–D: Anti‐inflammatory Macrolide Lactams with Unique Ring Systems from an Arctic Actinomycete Strain.
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- Angewandte Chemie, 2023, v. 135, n. 18, p. 1, doi. 10.1002/ange.202218085
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Didepside Formation by the Nonreducing Polyketide Synthase Preu6 of Preussia isomera Requires Interaction of Starter Acyl Transferase and Thioesterase Domains.
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- Angewandte Chemie, 2023, v. 135, n. 6, p. 1, doi. 10.1002/ange.202214379
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Coordination of Polyketide Release and Multiple Detoxification Pathways for Tolerable Production of Fungal Mycotoxins.
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- Angewandte Chemie, 2023, v. 135, n. 5, p. 1, doi. 10.1002/ange.202214814
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Cytochrome P450 Catalyzes Benzene Ring Formation in the Biosynthesis of Trialkyl‐Substituted Aromatic Polyketides.
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- Angewandte Chemie, 2023, v. 135, n. 5, p. 1, doi. 10.1002/ange.202214026
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Reshaping the 2‐Pyrone Synthase Active Site for Chemoselective Biosynthesis of Polyketides.
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- Angewandte Chemie, 2023, v. 135, n. 5, p. 1, doi. 10.1002/ange.202212440
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An Atypical Acyl‐CoA Synthetase Enables Efficient Biosynthesis of Extender Units for Engineering a Polyketide Carbon Scaffold.
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- Angewandte Chemie, 2022, v. 134, n. 43, p. 1, doi. 10.1002/ange.202208734
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Structure of a Promiscuous Thioesterase Domain Responsible for Branching Acylation in Polyketide Biosynthesis.
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- Angewandte Chemie, 2022, v. 134, n. 39, p. 1, doi. 10.1002/ange.202206385
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Innenrücktitelbild: Investigation of the Molecular Landscape of Bacterial Aromatic Polyketides by Global Analysis of Type II Polyketide Synthases (Angew. Chem. 24/2022).
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- Angewandte Chemie, 2022, v. 134, n. 24, p. 1, doi. 10.1002/ange.202206425
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Investigation of the Molecular Landscape of Bacterial Aromatic Polyketides by Global Analysis of Type II Polyketide Synthases.
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- Angewandte Chemie, 2022, v. 134, n. 24, p. 1, doi. 10.1002/ange.202202286
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A Pair of Atypical KAS III Homologues with Initiation and Elongation Functions Program the Polyketide Biosynthesis in Asukamycin.
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- Angewandte Chemie, 2022, v. 134, n. 19, p. 1, doi. 10.1002/ange.202200879
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Modular Halogenation, α‐Hydroxylation, and Acylation by a Remarkably Versatile Polyketide Synthase.
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- Angewandte Chemie, 2022, v. 134, n. 11, p. 1, doi. 10.1002/ange.202116614
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Catalytic Control of Spiroketal Formation in Rubromycin Polyketide Biosynthesis.
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- Angewandte Chemie, 2021, v. 133, n. 52, p. 27166, doi. 10.1002/ange.202109384
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An NADPH‐Dependent Ketoreductase Catalyses the Tetracyclic to Pentacyclic Skeletal Rearrangement in Chartreusin Biosynthesis.
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- Angewandte Chemie, 2021, v. 133, n. 50, p. 26582, doi. 10.1002/ange.202112047
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Biochemistry‐Guided Prediction of the Absolute Configuration of Fungal Reduced Polyketides.
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- Angewandte Chemie, 2021, v. 133, n. 43, p. 23591, doi. 10.1002/ange.202110658
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Biomimetic Total Synthesis of Enterocin.
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- Angewandte Chemie, 2021, v. 133, n. 37, p. 20431, doi. 10.1002/ange.202108157
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Biosynthesis of 6‐Hydroxymellein Requires a Collaborating Polyketide Synthase‐like Enzyme.
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- Angewandte Chemie, 2021, v. 133, n. 20, p. 11524, doi. 10.1002/ange.202100969
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Innenrücktitelbild: One Polyketide Synthase, Two Distinct Products: Trans‐Acting Enzyme‐Controlled Product Divergence in Calbistrin Biosynthesis (Angew. Chem. 16/2021).
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- Angewandte Chemie, 2021, v. 133, n. 16, p. 9227, doi. 10.1002/ange.202102305
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One Polyketide Synthase, Two Distinct Products: Trans‐Acting Enzyme‐Controlled Product Divergence in Calbistrin Biosynthesis.
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- Angewandte Chemie, 2021, v. 133, n. 16, p. 8933, doi. 10.1002/ange.202016525
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The Total Synthesis of Chondrochloren A.
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- Angewandte Chemie, 2021, v. 133, n. 13, p. 7014, doi. 10.1002/ange.202016072
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Mild C–C Bond Formation via Lewis Acid Catalyzed Oxetane Ring Opening with Soft Carbon Nucleophiles.
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- Angewandte Chemie, 2021, v. 133, n. 5, p. 2700, doi. 10.1002/ange.202013062
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Insect‐Associated Bacteria Assemble the Antifungal Butenolide Gladiofungin by Non‐Canonical Polyketide Chain Termination.
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- Angewandte Chemie, 2020, v. 132, n. 51, p. 23322, doi. 10.1002/ange.202005711
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Cross‐Module Enoylreduction in the Azalomycin F Polyketide Synthase.
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- Angewandte Chemie, 2020, v. 132, n. 50, p. 22926, doi. 10.1002/ange.202011357
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Catalyst‐Controlled Transannular Polyketide Cyclization Cascades: Selective Folding of Macrocyclic Polyketides.
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- Angewandte Chemie, 2020, v. 132, n. 42, p. 18548, doi. 10.1002/ange.202005733
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Shimalactone Biosynthesis Involves Spontaneous Double Bicyclo‐Ring Formation with 8π‐6π Electrocyclization.
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- Angewandte Chemie, 2020, v. 132, n. 22, p. 8542, doi. 10.1002/ange.202001024
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Genome Mining of Oxidation Modules in trans‐Acyltransferase Polyketide Synthases Reveals a Culturable Source for Lobatamides.
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- Angewandte Chemie, 2020, v. 132, n. 20, p. 7835, doi. 10.1002/ange.201916005
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Polyketide Cyclizations for the Synthesis of Polyaromatics.
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- Angewandte Chemie, 2020, v. 132, n. 18, p. 7039, doi. 10.1002/ange.201911255
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Loss of Single‐Domain Function in a Modular Assembly Line Alters the Size and Shape of a Complex Polyketide.
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- Angewandte Chemie, 2019, v. 131, n. 50, p. 18420, doi. 10.1002/ange.201911315
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Activation and Characterization of Cryptic Gene Cluster: Two Series of Aromatic Polyketides Biosynthesized by Divergent Pathways.
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- Angewandte Chemie, 2019, v. 131, n. 50, p. 18214, doi. 10.1002/ange.201910882
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Stereochemical Determination of Tuscolid/Tuscorons and Total Synthesis of Tuscoron D and E: Insights into the Tuscolid/Tuscoron Rearrangement.
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- Angewandte Chemie, 2019, v. 131, n. 37, p. 13153, doi. 10.1002/ange.201906166
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