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Isolation and Biosynthesis of Preussin B, a Pyrrolidine Alkaloid from Simplicillium lanosoniveum

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/anie.200805554openalex-snapshot
A Hybrid Organic/Inorganic Benzene
inferredcites →https://doi.org/10.1002/cbic.200400138openalex-snapshot
Fusarin C Biosynthesis in Fusarium moniliforme and Fusarium venenatum
inferredcites →https://doi.org/10.1002/cbic.200700202openalex-snapshot
Identification of a Hybrid PKS/NRPS Required for Pseurotin A Biosynthesis in the Human Pathogen Aspergillus fumigatus
inferredcites →https://doi.org/10.1002/cbic.200700390openalex-snapshot
Authentic Heterologous Expression of the Tenellin Iterative Polyketide Synthase Nonribosomal Peptide Synthetase Requires Coexpression with an Enoyl Reductase
inferredcites →https://doi.org/10.1002/cbic.200900187openalex-snapshot
A New Type of Pyrrolidine Biosynthesis Is Involved in the Late Steps of Xenocoumacin Production in Xenorhabdus nematophila
inferredcites →https://doi.org/10.1002/cbic.201000259openalex-snapshot
First Heterologous Reconstruction of a Complete Functional Fungal Biosynthetic Multigene Cluster
inferredcites →https://doi.org/10.1002/hlca.201000283openalex-snapshot
Ophiobolin Sesterterpenoids and Pyrrolidine Alkaloids from the Sponge‐Derived Fungus Aspergillus ustus
inferredcites →https://doi.org/10.1006/viro.2002.1567openalex-snapshot
New Targets for Antivirals: The Ribosomal A-Site and the Factors That Interact with It
inferredcites →https://doi.org/10.1007/bf01240602openalex-snapshot
Ladybird defence alkaloids: Structural, chemotaxonomic and biosynthetic aspects (Col.: Coccinellidae)
inferredcites →https://doi.org/10.1016/j.mycres.2008.09.008openalex-snapshot
Systematics and evolution of the genus Torrubiella (Hypocreales, Ascomycota)
inferredcites →https://doi.org/10.1016/s0040-4020(01)00292-7openalex-snapshot
A concise synthesis of (+)-preussin
inferredcites →https://doi.org/10.1021/ar040247ropenalex-snapshot
Bioactive Substances from Insect Pathogenic Fungi
inferredcites →https://doi.org/10.1021/ja01573a076openalex-snapshot
The Biogenesis of Nicotine. III. Further Observations on the Incorporation of Ornithine into the Pyrrolidine Ring1
inferredcites →https://doi.org/10.1021/ja048345vopenalex-snapshot
Biosynthesis of Lambertellols Based on the High Specific Incorporation of the 13C-Labeled Acetates and Their Biological Properties
inferredcites →https://doi.org/10.1021/ja107084dopenalex-snapshot
Analysis of Intact and Dissected Fungal Polyketide Synthase-Nonribosomal Peptide Synthetase in Vitro and in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1021/ja807052copenalex-snapshot
Late Stage Oxidations during the Biosynthesis of the 2-Pyridone Tenellin in the Entomopathogenic Fungus Beauveria bassiana
inferredcites →https://doi.org/10.1021/np020430yopenalex-snapshot
Novel Tetramic Acids and Pyridone Alkaloids, Militarinones B, C, and D, from the Insect Pathogenic Fungus Paecilomyces militaris
inferredcites →https://doi.org/10.1021/np0580560openalex-snapshot
Alkaloids from Amphibian Skin: A Tabulation of Over Eight-Hundred Compounds
inferredcites →https://doi.org/10.1021/np070494eopenalex-snapshot
Aurovertins F–H from the Entomopathogenic Fungus Metarhizium anisopliae
inferredcites →https://doi.org/10.1021/np200035mopenalex-snapshot
Marianins A and B, Prenylated Phenylpropanoids from Mariannaea camptospora
inferredcites →https://doi.org/10.1021/np800088aopenalex-snapshot
Natural Products Chemistry and Taxonomy of the Marine Cyanobacterium Blennothrix cantharidosmum
inferredcites →https://doi.org/10.1021/ol0606435openalex-snapshot
A Concise Stereoselective Synthesis of Preussin, 3-epi-Preussin, and Analogues
inferredcites →https://doi.org/10.1021/ol101631eopenalex-snapshot
A Concise and Stereoselective Synthesis of Hydroxypyrrolidines: Rapid Synthesis of (+)-Preussin
inferredcites →https://doi.org/10.1021/ol401975zopenalex-snapshot
Aogacillins A and B Produced by Simplicillium sp. FKI-5985: New Circumventors of Arbekacin Resistance in MRSA
inferredcites →https://doi.org/10.1038/nchembio869openalex-snapshot
Genomics-driven discovery of PKS-NRPS hybrid metabolites from Aspergillus nidulans
inferredcites →https://doi.org/10.1039/a707613dopenalex-snapshot
Pyrrole, pyrrolidine, pyridine, piperidine and tropane alkaloids (1998 to 1999)
inferredcites →https://doi.org/10.1039/b100918oopenalex-snapshot
Endophytes: a rich source of functional metabolites (1987 to 2000)
inferredcites →https://doi.org/10.1039/b702378bopenalex-snapshot
Epicoccarines A, B and epipyridone: tetramic acids and pyridone alkaloids from an Epicoccum sp. associated with the tree fungus Pholiota squarrosa
inferredcites →https://doi.org/10.1039/np9840100225openalex-snapshot
Pyrrolidine, piperidine, and pyridine alkaloids
inferredcites →https://doi.org/10.1039/np9941100581openalex-snapshot
Pyrrole, pyrrolidine, pyridine, piperidine, and azepine alkaloids
inferredcites →https://doi.org/10.1039/np9971400637openalex-snapshot
Pyrrole, pyrrolidine pyridine, piperidine, azepine and tropane alkaloids
inferredcites →https://doi.org/10.1046/j.1365-313x.1993.04020215.xopenalex-snapshot
Proline biosynthesis and osmoregulation in plants
inferredcites →https://doi.org/10.1127/nova.hedwigia/71/2001/1openalex-snapshot
A revision of Verticillium section Prostrata. IV. The genera Lecanicillium and Simplicillium gen. nov.
inferredcites →https://doi.org/10.1127/nova.hedwigia/73/2001/1openalex-snapshot
A revision of Verticillium section Prostrata. IV. The genera Lecanicillium and Simplicillium gen. nov.°)
inferredcites →https://doi.org/10.1128/aac.44.10.2794-2801.2000openalex-snapshot
Inhibition of Cyclin-Dependent Kinase Activity and Induction of Apoptosis by Preussin in Human Tumor Cells
inferredcites →https://doi.org/10.1146/annurev.pp.45.060194.001353openalex-snapshot
Alkaloid Biogenesis: Molecular Aspects
inferredcites →https://doi.org/10.1271/bbb.66.1093openalex-snapshot
Short-step Syntheses of All Stereoisomers of Preussin and Their Bioactivities
inferredcites →https://doi.org/10.3114/sim.2007.57.01openalex-snapshot
Phylogenetic classification of Cordyceps and the clavicipitaceous fungi
inferredcites →https://doi.org/10.7164/antibiotics.41.1774openalex-snapshot
L-657,398, a novel antifungal agent: Fermentation, isolation, structural elucidation and biological properties.
inferredcites →https://doi.org/10.7164/antibiotics.42.1184openalex-snapshot
The relative and absolute stereochemistry of the antifungal agent preussin.
inferredcites →https://doi.org/10.7164/antibiotics.48.630openalex-snapshot
Gualamycin, a Novel Acaricide Produced by Streptomyces sp. NK11687. II. Structural Elucidation.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.11646/phytotaxa.379.1.6zenodo-depositor-declared
Akanthomyces araneogenum, a new Isaria-like araneogenous species
inferred← citeshttps://doi.org/10.11646/phytotaxa.521.2.2zenodo-depositor-declared
Simplicillium pech-merlensis, a new fungal species isolated from the air of the Pech-Merle show cave
inferred← citeshttps://doi.org/10.5281/zenodo.18051776zenodo-depositor-declared
inferred← citeshttps://doi.org/10.1002/9783527807253.ch5openalex-snapshot
Catalytic Addition Reactions
inferred← citeshttps://doi.org/10.1002/adsc.202100038openalex-snapshot
Photocatalytic Deoxygenative Carboimination towards Functionalized Pyrrolines by Using Unstrained γ,δ‐Unsaturated Oximes
inferred← citeshttps://doi.org/10.1002/ange.201611816openalex-snapshot
Gold‐Catalyzed [3+2]/Retro‐[3+2]/[3+2] Cycloaddition Cascade Reaction of N‐Alkoxyazomethine Ylides
inferred← citeshttps://doi.org/10.1002/anie.201611816openalex-snapshot
Gold‐Catalyzed [3+2]/Retro‐[3+2]/[3+2] Cycloaddition Cascade Reaction of N‐Alkoxyazomethine Ylides
inferred← citeshttps://doi.org/10.1002/bab.2281openalex-snapshot
The genus Simplicillium and Emericellopsis: A review of phytochemistry and pharmacology
inferred← citeshttps://doi.org/10.1002/chem.202300296openalex-snapshot
Catalytic Enantioselective [3+2] Cycloaddition of N‐Metalated Azomethine Ylides
inferred← citeshttps://doi.org/10.1007/978-981-16-3307-2_18openalex-snapshot
Bioprospecting of Marine Fungi
inferred← citeshttps://doi.org/10.1007/s10593-022-03052-3openalex-snapshot
Synthesis, hydrolysis, and reductive cyclization of ethyl 5-chloro-4-(4-nitropyrrolidin-3-yl)pyrrole-3-carboxylates
inferred← citeshttps://doi.org/10.1007/s11426-014-5270-0openalex-snapshot
The first enantioselective total synthesis of (+)-preussin B and an improved synthesis of (+)-preussin by step-economical methods
inferred← citeshttps://doi.org/10.1016/j.arabjc.2022.104095openalex-snapshot
Iron-catalyzed synthesis of N-heterocycles via intermolecular and intramolecular cyclization reactions: A review
inferred← citeshttps://doi.org/10.1016/j.bmc.2025.118336openalex-snapshot
Synthesis and lipid-lowering activities of preussin derivatives
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104286openalex-snapshot
Depsidones and a dihydroxanthenone from the endophytic fungi Simplicillium lanosoniveum (J.F.H. Beyma) Zare & W. Gams PSU-H168 and PSU-H261
inferred← citeshttps://doi.org/10.1016/j.micpath.2020.104248openalex-snapshot
Structural deformation in pathogenic bacteria cells caused by marine fungal metabolites: An in vitro investigation
inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.08.002openalex-snapshot
Depsidones and an α-pyrone derivative from Simpilcillium sp. PSU-H41, an endophytic fungus from Hevea brasiliensis leaf
inferred← citeshttps://doi.org/10.1016/j.tet.2016.04.032openalex-snapshot
Eight linear peptides from the deep-sea-derived fungus Simplicillium obclavatum EIODSF 020
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00662openalex-snapshot
Preussins with Inhibition of IL-6 Expression from Aspergillus flocculosus 16D-1, a Fungus Isolated from the Marine Sponge Phakellia fusca
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00670openalex-snapshot
Sulfamidate-Based Stereoselective Total Synthesis of (+)-Preussin Using Gold(I)-Catalyzed Intramolecular Dehydrative Amination: Dead End and Detour
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00362openalex-snapshot
Asymmetric Syntheses of (+)-Preussin B, the C(2)-Epimer of (−)-Preussin B, and 3-Deoxy-(+)-preussin B
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00361openalex-snapshot
Molecular Iodine-Mediated α-C–H Oxidation of Pyrrolidines to N,O-Acetals: Synthesis of (±)-Preussin by Late-Stage 2,5-Difunctionalizations of Pyrrolidine
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02412openalex-snapshot
Ag(I)-Fesulphos-Catalyzed Enantioselective Synthesis of 3-Silylproline Derivatives
inferred← citeshttps://doi.org/10.1021/jo5011558openalex-snapshot
Three-Step Synthesis of (±)-Preussin from Decanal
inferred← citeshttps://doi.org/10.1038/ja.2014.165openalex-snapshot
Tolypoalbin, a new tetramic acid from Tolypocladium album TAMA 479
inferred← citeshttps://doi.org/10.1038/s41429-017-0015-xopenalex-snapshot
Two new secondary metabolites from a fungus of the genus Robillarda
inferred← citeshttps://doi.org/10.1038/s41598-021-94893-zopenalex-snapshot
Taxonomic and phylogenetic characterizations reveal four new species of Simplicillium (Cordycipitaceae, Hypocreales) from Guizhou, China
inferred← citeshttps://doi.org/10.1038/s41598-025-04162-6openalex-snapshot
Cytotoxicity evaluation and metabolomic profiling of Spheciospongia vagabunda-associated fungi corroborated by in silico studies
inferred← citeshttps://doi.org/10.1038/s41598-025-12456-yopenalex-snapshot
Molecular networking derived from untargeted LC-MS/MS analysis to discover inhibitors of RANKL-induced osteoclastogenesis from Egyptian marine sponge-associated fungi
inferred← citeshttps://doi.org/10.1039/c4ob02454kopenalex-snapshot
Domino [4 + 1]-annulation of α,β-unsaturated δ-amino esters with Rh( ii )–carbenoids – a new approach towards multi-functionalized N-aryl pyrrolidines
inferred← citeshttps://doi.org/10.1039/c6ob02523dopenalex-snapshot
An efficient approach to trans-4-hydroxy-5-substituted 2-pyrrolidinones through a stereoselective tandem Barbier process: divergent syntheses of (3R,4S)-statines, (+)-preussin and (−)-hapalosin
inferred← citeshttps://doi.org/10.1039/c8ob02645aopenalex-snapshot
Alkoxyallene-based syntheses of preussin and its analogs and their cytotoxicity
inferred← citeshttps://doi.org/10.1039/d0cc02784gopenalex-snapshot
Iron-catalyzed carbonylative cyclization of γ,δ-unsaturated aromatic oxime esters to functionalized pyrrolines
inferred← citeshttps://doi.org/10.1039/d0qo01064bopenalex-snapshot
Copper-catalyzed borylative cyclization of γ,δ-unsaturated aromatic oxime esters to (borylmethyl)pyrrolidines
inferred← citeshttps://doi.org/10.1080/14786419.2017.1343320openalex-snapshot
A new antibiotic produced by the cyanobacterium-symbiotic fungus Simplicillium lanosoniveum
inferred← citeshttps://doi.org/10.1128/mra.00366-20openalex-snapshot
Draft Genome Sequence of Simplicillium aogashimaense 72-15.1, a Putative Endophyte of Brachiaria brizantha
inferred← citeshttps://doi.org/10.1134/s1070363221110141openalex-snapshot
Synthesis of Ethyl 3-Methyl-4,5-dioxo-1,2-diphenylpyrrolidine-3-carboxylate Analogues Using Green and Expeditious Grinding Method
inferred← citeshttps://doi.org/10.3390/antibiotics9110753openalex-snapshot
Simplicilones A and B Isolated from the Endophytic Fungus Simplicillium subtropicum SPC3
inferred← citeshttps://doi.org/10.3390/jof7110964openalex-snapshot
Entomopathogenic Potential of Simplicillium lanosoniveum Native Strain in Suppressing Invasive Whitefly, Aleurodicus rugioperculatus Martin (Hemiptera: Aleyrodidae), Infesting Coconut
inferred← citeshttps://doi.org/10.3390/md16040119openalex-snapshot
Bis-Indolyl Benzenoids, Hydroxypyrrolidine Derivatives and Other Constituents from Cultures of the Marine Sponge-Associated Fungus Aspergillus candidus KUFA0062
inferred← citeshttps://doi.org/10.3390/md21030166openalex-snapshot
Effects and Mechanisms of Action of Preussin, a Marine Fungal Metabolite, against the Triple-Negative Breast Cancer Cell Line, MDA-MB-231, in 2D and 3D Cultures
inferred← citeshttps://doi.org/10.3390/ph16121652openalex-snapshot
Phytochemicals as Immunomodulatory Molecules in Cancer Therapeutics
inferred← citeshttps://doi.org/10.3897/mycokeys.58.37176openalex-snapshot
Three novel insect-associated species of Simplicillium (Cordycipitaceae, Hypocreales) from Southwest China
inferred← citeshttps://doi.org/10.3897/mycokeys.60.38040openalex-snapshot
The genus Simplicillium
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