Works matching DE "DIKETOPIPERAZINES"
Results: 178
Diketopiperazines and other bioactive compounds from bacterial symbionts of marine sponges.
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- Antonie van Leeuwenhoek, 2020, v. 113, n. 7, p. 875, doi. 10.1007/s10482-020-01398-2
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New Sulfur-Containing Diketopiperazine from Marine-Derived Bacteria Streptomyces rochei sp. 81 with Potent Carbonic Anhydrase II Inhibition.
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- Chemistry of Natural Compounds, 2023, v. 59, n. 2, p. 346, doi. 10.1007/s10600-023-03990-0
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Indole Alkaloids from the Cigar Tobacco-Derived Endophytic Fungus Aspergillus oryzae and Their Antibacterial Activity.
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- Chemistry of Natural Compounds, 2022, v. 58, n. 6, p. 1093, doi. 10.1007/s10600-022-03872-x
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Two New CPA-Type Indole Alkaloids from the Tobacco-Derived Fungus Aspergillus versicolor and the Anti-TMV Activity.
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- Chemistry of Natural Compounds, 2022, v. 58, n. 5, p. 888, doi. 10.1007/s10600-022-03822-7
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Two New CPA-Type Indole Alkaloids from the Tobacco-Derived Fungus Aspergillus oryzae and Anti-TMV Activity.
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- Chemistry of Natural Compounds, 2022, v. 58, n. 4, p. 717, doi. 10.1007/s10600-022-03775-x
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Aspergillines K and L, Two New Anti-TMV Indole Alkaloids from Fungus Aspergillus versicolor Derived from Tobacco.
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- Chemistry of Natural Compounds, 2022, v. 58, n. 4, p. 712, doi. 10.1007/s10600-022-03774-y
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2,5-Diketopiperazines from Aspergillus sp., the Endophytic Fungus of Astragalus membranaceus and their Anticancer Assay.
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- Chemistry of Natural Compounds, 2020, v. 56, n. 3, p. 583, doi. 10.1007/s10600-020-03100-4
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Diketopiperazine Alkaloids and Steroids from a Marine-Derived Pleosporales sp. Fungus.
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- Chemistry of Natural Compounds, 2018, v. 54, n. 4, p. 818, doi. 10.1007/s10600-018-2487-8
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A New Diketopiperazine of Nocardiopsis alba Isolated from Anthogorgia caerulea.
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- Chemistry of Natural Compounds, 2017, v. 53, n. 2, p. 338, doi. 10.1007/s10600-017-1983-6
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Diketopiperazines from Cultures of Rhodococcus rhodochrous.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 6, p. 1157, doi. 10.1007/s10600-016-1894-y
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Secondary Metabolites Isolated from the Sponge-Associated Fungus Nigrospora oryzae.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 5, p. 969, doi. 10.1007/s10600-016-1837-7
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Diketopiperazines from Marine Isolate of Actinobacterium Nocardiopsis umidischolae KMM 7036.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 1, p. 192, doi. 10.1007/s10600-015-1242-7
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Two New Diketopiperazines from ARUM Palaestinum.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 6, p. 1075, doi. 10.1007/s10600-014-1162-y
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Alkaloids and Nucleoside Derivatives from a Fungal Endophyte of Huperzia serrata.
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- Chemistry of Natural Compounds, 2013, v. 49, n. 1, p. 184, doi. 10.1007/s10600-013-0553-9
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Bromophenol coupled with diketopiperazine from marine red alga Symphyocladia latiuscula.
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- Chemistry of Natural Compounds, 2012, v. 48, n. 4, p. 622, doi. 10.1007/s10600-012-0327-9
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A Diketopiperazine, Cyclo -(L-Pro-L-Ile), Derived From Bacillus thuringiensis JCK-1233 Controls Pine Wilt Disease by Elicitation of Moderate Hypersensitive Reaction.
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- Frontiers in Plant Science, 2020, v. 11, p. 1, doi. 10.3389/fpls.2020.01023
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Detection of diketopiperazine and pyrrolnitrin, compounds with anti-Pythium insidiosum activity, in a Pseudomonas stutzeri environmental strain.
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- Biomedical Papers of the Medical Faculty of Palacky University in Olomouc, 2014, v. 158, n. 3, p. 378, doi. 10.5507/bp.2012.090
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Penicillium roqueforti: a multifunctional cell factory of high value-added molecules.
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- Journal of Applied Microbiology, 2015, v. 118, n. 4, p. 781, doi. 10.1111/jam.12706
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Identification of antimicrobial compound, diketopiperazines, from a Bacillus sp. N strain associated with a rhabditid entomopathogenic nematode against major plant pathogenic fungi.
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- Journal of Applied Microbiology, 2012, v. 113, n. 4, p. 914, doi. 10.1111/j.1365-2672.2012.05385.x
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The tRNA-Dependent Biosynthesis of Modified Cyclic Dipeptides.
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- International Journal of Molecular Sciences, 2014, v. 15, n. 8, p. 14610, doi. 10.3390/ijms150814610
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Antifungal Activity of Diketopiperazines and Stilbenes Against Plant Pathogenic Fungi In Vitro.
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- Applied Biochemistry & Biotechnology, 2014, v. 172, n. 2, p. 741, doi. 10.1007/s12010-013-0567-6
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Activity and Synergistic Antimicrobial Activity Between Diketopiperazines Against Bacteria In Vitro.
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- Applied Biochemistry & Biotechnology, 2012, v. 168, n. 8, p. 2285, doi. 10.1007/s12010-012-9937-8
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A Plausible Simultaneous Synthesis of Amino Acids and Simple Peptides on the Primordial Earth.
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- Angewandte Chemie, 2014, v. 126, n. 31, p. 8270, doi. 10.1002/ange.201403683
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Enantioselective Total Synthesis of (−)-Lansai B and (+)-Nocardioazines A and B.
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- Angewandte Chemie, 2014, v. 126, n. 24, p. 6320, doi. 10.1002/ange.201402571
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2,5-Diketopiperazines: A New Class of Poly(ADP-D. K. Nilov1ribose)polymerase Inhibitors.
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- Biochemistry (00062979), 2018, v. 83, n. 2, p. 152, doi. 10.1134/S0006297918020074
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Characterisation of Cooked Cheese Flavour: Non-Volatile Components.
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- Foods, 2023, v. 12, n. 20, p. 3749, doi. 10.3390/foods12203749
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Inhibition of Aflatoxin Production in Aspergillus flavus by a Klebsiella sp. and Its Metabolite Cyclo(l-Ala-Gly).
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- Toxins, 2024, v. 16, n. 3, p. 141, doi. 10.3390/toxins16030141
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Self-Assembly of Homo- and Hetero-Chiral Cyclodipeptides into Supramolecular Polymers towards Antimicrobial Gels.
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- Polymers (20734360), 2022, v. 14, n. 21, p. 4554, doi. 10.3390/polym14214554
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Structure and further fragmentation of significant [a<sub>3</sub> + Na − H]<sup>+</sup> ions from sodium-cationized peptides.
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- Journal of Mass Spectrometry, 2015, v. 50, n. 1, p. 212, doi. 10.1002/jms.3520
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Convenient Synthesis of 1,3,4,6-Tetrasubstituted 2,5-Diketopiperazines.
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- ARKIVOC: Online Journal of Organic Chemistry, 2016, p. 100, doi. 10.3998/ark.5550190.p009.532
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First highly stereocontrolled synthesis of tetrahydro trans-β-carboline derivatives by exploiting the influence of a cyclic amide.
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- ARKIVOC: Online Journal of Organic Chemistry, 2013, p. 22
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Separation of five diketopiperazines from the marine fungus Alternaria alternate HK‐25 by high‐speed counter‐current chromatography.
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- Journal of Separation Science, 2019, v. 42, n. 15, p. 2510, doi. 10.1002/jssc.201801284
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New diketopiperazines as vectors for peptide protection and brain delivery: Synthesis and biological evaluation.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2016, v. 59, n. 12, p. 517, doi. 10.1002/jlcr.3442
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Cyclodipeptides: From Their Green Synthesis to Anti-Age Activity.
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- Biomedicines, 2022, v. 10, n. 10, p. N.PAG, doi. 10.3390/biomedicines10102342
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Chemical Investigation of Diketopiperazines and N-Phenethylacetamide Isolated from Aquimarina sp. MC085 and Their Effect on TGF-β-Induced Epithelial–Mesenchymal Transition.
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- Applied Sciences (2076-3417), 2021, v. 11, n. 19, p. 8866, doi. 10.3390/app11198866
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Positive Regulation of Spoilage Potential and Biofilm Formation in Shewanella baltica OS155 via Quorum Sensing System Composed of DKP and Orphan LuxRs.
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- Frontiers in Microbiology, 2019, p. N.PAG, doi. 10.3389/fmicb.2019.00135
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Separation of Cyclic Dipeptides (Diketopiperazines) from Their Corresponding Linear Dipeptides by RP-HPLC and Method Validation.
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- Chromatography Research International, 2013, p. 1, doi. 10.1155/2013/310269
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Potential Emergence of Multi-quorum Sensing Inhibitor Resistant (MQSIR) Bacteria.
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- Indian Journal of Microbiology, 2016, v. 56, n. 1, p. 1, doi. 10.1007/s12088-015-0558-0
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- Article
Dexrazoxane provided moderate protection in a catecholamine model of severe cardiotoxicity.
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- Canadian Journal of Physiology & Pharmacology, 2012, v. 90, n. 4, p. 473, doi. 10.1139/y2012-009
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Design, Semisynthesis, Insecticidal and Antibacterial Activities of a Series of Marine-Derived Geodin Derivatives and Their Preliminary Structure–Activity Relationships.
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- Marine Drugs, 2022, v. 20, n. 2, p. N.PAG, doi. 10.3390/md20020082
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Secondary Metabolites from Marine-Derived Fungi and Actinobacteria as Potential Sources of Novel Colorectal Cancer Drugs.
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- Marine Drugs, 2022, v. 20, n. 1, p. 67, doi. 10.3390/md20010067
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Untapped Potential of Marine-Associated Cladosporium Species: An Overview on Secondary Metabolites, Biotechnological Relevance, and Biological Activities.
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- Marine Drugs, 2021, v. 19, n. 11, p. 645, doi. 10.3390/md19110645
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Apoptotic Activity of New Oxisterigmatocystin Derivatives from the Marine-Derived Fungus Aspergillus nomius NC06.
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- Marine Drugs, 2021, v. 19, n. 11, p. 631, doi. 10.3390/md19110631
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Fusaripyridines A and B; Highly Oxygenated Antimicrobial Alkaloid Dimers Featuring an Unprecedented 1,4-Bis(2-hydroxy-1,2-dihydropyridin-2-yl)butane-2,3-dione Core from the Marine Fungus Fusarium sp. LY019.
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- Marine Drugs, 2021, v. 19, n. 9, p. 505, doi. 10.3390/md19090505
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Molecular Networking-Guided Isolation of New Etzionin-Type Diketopiperazine Hydroxamates from the Persian Gulf Sponge Cliona celata.
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- Marine Drugs, 2021, v. 19, n. 8, p. 439, doi. 10.3390/md19080439
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Structures and Biological Activities of Diketopiperazines from Marine Organisms: A Review.
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- Marine Drugs, 2021, v. 19, n. 8, p. 403, doi. 10.3390/md19080403
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OVAT Analysis and Response Surface Methodology Based on Nutrient Sources for Optimization of Pigment Production in the Marine-Derived Fungus Talaromyces albobiverticillius 30548 Submerged Fermentation.
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- Marine Drugs, 2021, v. 19, n. 5, p. 248, doi. 10.3390/md19050248
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New Andrastin-Type Meroterpenoids from the Marine-Derived Fungus Penicillium sp.
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- Marine Drugs, 2021, v. 19, n. 4, p. 189, doi. 10.3390/md19040189
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Bioactive Indole Diketopiperazine Alkaloids from the Marine Endophytic Fungus Aspergillus sp. YJ191021.
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- Marine Drugs, 2021, v. 19, n. 3, p. 157, doi. 10.3390/md19030157
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New Prenylated Indole Homodimeric and Pteridine Alkaloids from the Marine-Derived Fungus Aspergillus austroafricanus Y32-2.
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- Marine Drugs, 2021, v. 19, n. 2, p. 98, doi. 10.3390/md19020098
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