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Bridged Epipolythiodiketopiperazines from Penicillium raciborskii, an Endophytic Fungus of Rhododendron tomentosum Harmaja

https://doi.org/10.1021/np500822k
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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/jms.1166openalex-snapshot
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inferredcites →https://doi.org/10.1007/s13225-010-0087-4openalex-snapshot
Bioactivity and genetic diversity of endophytic fungi in Rhododendron tomentosum Harmaja
inferredcites →https://doi.org/10.1016/0040-4020(80)80155-4openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.cclet.2008.09.006openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.jbiosc.2010.06.007openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.jbiotec.2005.10.015openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.phytochem.2007.07.014openalex-snapshot
Penicidones A–C, three cytotoxic alkaloidal metabolites of an endophytic Penicillium sp.
inferredcites →https://doi.org/10.1016/j.phytochem.2008.04.003openalex-snapshot
Metabolites from the endophytic fungus Xylaria sp. PSU-D14
inferredcites →https://doi.org/10.1016/j.theochem.2008.09.021openalex-snapshot
Scaling factors for carbon NMR chemical shifts obtained from DFT B3LYP calculations
inferredcites →https://doi.org/10.1016/s1286-4579(03)00073-xopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ac071447uopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ja970112zopenalex-snapshot
Computed 13 C NMR Chemical Shifts via Empirically Scaled GIAO Shieldings and Molecular Mechanics Geometries. Conformation and Configuration from 13 C Shifts
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Antimalarial Benzoquinones from an Endophytic Fungus, Xylaria sp.
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inferredcites →https://doi.org/10.1021/np200254topenalex-snapshot
Dereplication of Microbial Natural Products by LC-DAD-TOFMS
inferredcites →https://doi.org/10.1021/ol061046lopenalex-snapshot
Transformation of an Irregularly Bridged Epidithiodiketopiperazine to Trichodermamide A
inferredcites →https://doi.org/10.1038/ja.2010.99openalex-snapshot
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CRC Handbook of Medicinal Herbs
inferredcites →https://doi.org/10.1111/j.1365-2672.2009.04285.xopenalex-snapshot
Aspergillus fumigatusFresenius, an endophytic fungus fromJuniperus communisL. Horstmann as a novel source of the anticancer pro-drug deoxypodophyllotoxin
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02773.xopenalex-snapshot
Fungal endophytes: diversity and functional roles
inferredcites →https://doi.org/10.1515/bc.2007.066openalex-snapshot
Inhibition of inducible tumor necrosis factor-α expression by the fungal epipolythiodiketopiperazine gliovirin
inferredcites →https://doi.org/10.3746/jfn.2006.11.2.100openalex-snapshot
Extracts and Essential Oil of Ledum palustre L. Leaves and Their Antioxidant and Antimicrobial Activities
inferredcites →https://doi.org/10.7164/antibiotics.35.1326openalex-snapshot
The structure of gliovirin, a new antibiotic from Gliocladium virens.
inferredcites →https://doi.org/10.7164/antibiotics.37.667openalex-snapshot
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What points at this work

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

inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.11.007zenodo-depositor-declared
Thiodiketopiperazines with two spirocyclic centers extracted from Botryosphaeria mamane, an endophytic fungus isolated from Bixa orellana L.
inferred← citeshttps://doi.org/10.1002/ange.202217212openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202404139openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202217212openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202404139openalex-snapshot
Synthesis of Unsymmetrical Trisulfides from S‐Substituted Sulphenylthiosulphates
inferred← citeshttps://doi.org/10.1002/bab.1721openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cbdv.202501797openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cbic.202000403openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-04675-0_6openalex-snapshot
An Update on Bioactive Natural Products from Endophytic Fungi of Medicinal Plants
inferred← citeshttps://doi.org/10.1007/978-3-030-14846-1_11openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-84126-3_9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-642-36202-6_199-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-13-9566-6_13openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-97-7312-1_13openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00044-024-03326-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10529-019-02677-3openalex-snapshot
Non-lipopeptide fungi-derived peptide antibiotics developed since 2000
inferred← citeshttps://doi.org/10.1007/s11418-021-01557-3openalex-snapshot
Exploration of marine natural resources in Indonesia and development of efficient strategies for the production of microbial halogenated metabolites
inferred← citeshttps://doi.org/10.1007/s13205-020-2081-1openalex-snapshot
Endophytic Penicillium species and their agricultural, biotechnological, and pharmaceutical applications
inferred← citeshttps://doi.org/10.1007/s13659-022-00365-wopenalex-snapshot
Untargeted metabolomics to evaluate antifungal mechanism: a study of Cophinforma mamane and Candida albicans interaction
inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00009-3openalex-snapshot
Bicyclic 6-6 Systems With One Bridgehead (Ring Junction) Nitrogen Atom: Two Extra Heteroatoms 1:1
inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00013-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00104-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-95241-5.00001-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-444-64179-3.00004-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.alkal.2025.01.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ejmech.2026.118854openalex-snapshot
Recent progress in marine natural products with 1,2-oxazine scaffold: structural diversity, biological potential and synthetic studies
inferred← citeshttps://doi.org/10.1016/j.jep.2019.02.010openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112338openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.phytol.2017.06.020openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jafc.4c00572openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00654openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b01283openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.8b03262openalex-snapshot
Unsymmetrical Organotrisulfide Formation via Low-Temperature Disulfanyl Anion Transfer to an Organothiosulfonate
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c04303openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacs.6c05481openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41429-020-0314-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41467-018-04306-5openalex-snapshot
Polysulfurating reagent design for unsymmetrical polysulfide construction
inferred← citeshttps://doi.org/10.1039/c6np90030eopenalex-snapshot
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Natural products with 1,2-oxazine scaffold: occurrence, chemical diversity, bioactivity, synthesis, and biosynthesis
inferred← citeshttps://doi.org/10.1039/d3ra03242fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d6ob00603eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1080/14786419.2019.1627348openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s12934-023-02118-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1248/yakushi.18-00221openalex-snapshot
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inferred← citeshttps://doi.org/10.1371/journal.pone.0158945openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fmicb.2022.857041openalex-snapshot
Thiodiketopiperazines and Alkane Derivatives Produced by the Mangrove Sediment–Derived Fungus Penicillium ludwigii SCSIO 41408
inferred← citeshttps://doi.org/10.3390/antibiotics12081273openalex-snapshot
Bioactive Naphtho-α-Pyranones from Two Endophytic Fungi of the Genus Polyphilus
inferred← citeshttps://doi.org/10.3390/ijms27031365openalex-snapshot
Mining the Hidden Pharmacopeia: Fungal Endophytes, Natural Products, and the Rise of AI-Driven Drug Discovery
inferred← citeshttps://doi.org/10.3390/jof4030077openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/jof7070570openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/jof8060628openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md14070122openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md20100597openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/microorganisms10020360openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules22122026openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules25020240openalex-snapshot
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inferred← citeshttps://doi.org/10.70675/f14e5b60z8366z4c09z8181zc33709374e2aopenalex-snapshot
Etude mycochimique et activités leishmanicides de composés issus de Botryosphaeria mamane, un champignon endophyte isolé de Bixa orellana L.
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