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Sesquiterpenoids isolated from an endophyte fungus Diaporthe sp.

https://doi.org/10.1039/c4ra13136c
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What this work says

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

inferredcites →https://doi.org/10.1002/1099-0690(200210)2002:19<3237::aid-ejoc3237>3.0.co;2-topenalex-snapshot
Novel α-L-Rhamnopyranosides from a Single Strain of Streptomyces by Supplement-Induced Biosynthetic Steps
inferredcites →https://doi.org/10.1002/1521-3773(20000915)39:18<3258::aid-anie3258>3.0.co;2-qopenalex-snapshot
Hexacyclinic acid, a Polyketide fromStreptomyces with a Novel Carbon Skeleton
inferredcites →https://doi.org/10.1016/j.jbiotec.2012.01.015openalex-snapshot
Differential expression of silent polyketide biosynthesis gene clusters in chemostat cultures of Aspergillus nidulans
inferredcites →https://doi.org/10.1016/s0031-9422(99)00199-5openalex-snapshot
Microbial hydroxylation of natural drimenic lactones
inferredcites →https://doi.org/10.1016/s0040-4020(01)00595-6openalex-snapshot
A new example of 1α-hydroxylation of drimanic terpenes through combined microbial and chemical processes
inferredcites →https://doi.org/10.1016/s0040-4039(00)60742-6openalex-snapshot
Viridianol, a rearranged sesquiterpene with a novel carbon skeleton from Laurencia viridis
inferredcites →https://doi.org/10.1016/s1367-5931(99)80022-2openalex-snapshot
Chemical biology paper alert
inferredcites →https://doi.org/10.1021/jm0495374openalex-snapshot
In Vitro Cytotoxic Activities of 2-Alkyl-4,6-diheteroalkyl-1,3,5-triazines: New Molecules in Anticancer Research
inferredcites →https://doi.org/10.1021/np000377iopenalex-snapshot
New Co-metabolites of the Streptazolin Pathway
inferredcites →https://doi.org/10.1021/np060076uopenalex-snapshot
Minor Sesquiterpenes with New Carbon Skeletons from the Brown Alga Dictyopteris divaricata
inferredcites →https://doi.org/10.1021/np070504bopenalex-snapshot
Uncovering Biosynthetic Potential of Plant-Associated Fungi: Effect of Culture Conditions on Metabolite Production by Paraphaeosphaeria quadriseptata and Chaetomium chiversii
inferredcites →https://doi.org/10.1021/np3004112openalex-snapshot
Sesquiterpenoids from the Mangrove-Derived Endophytic Fungus Diaporthe sp.
inferredcites →https://doi.org/10.1021/np400202fopenalex-snapshot
Guaiane-Type Sesquiterpenes from Curcuma phaeocaulis and Their Inhibitory Effects on Nitric Oxide Production
inferredcites →https://doi.org/10.1021/np400873vopenalex-snapshot
Anti-inflammatory Diterpenoids from the Roots of Euphorbia ebracteolata
inferredcites →https://doi.org/10.1021/np50076a016openalex-snapshot
New Sesquiterpenes and C15 Acetogenins from the Marine Red Alga Laurencia implicata
inferredcites →https://doi.org/10.1021/ol026506zopenalex-snapshot
Brasilane-Type Sesquiterpenoids from Laurencia obtusa
inferredcites →https://doi.org/10.1039/b821578bopenalex-snapshot
Triggering cryptic natural product biosynthesis in microorganisms
inferredcites →https://doi.org/10.1126/science.1155888openalex-snapshot
VelB/VeA/LaeA Complex Coordinates Light Signal with Fungal Development and Secondary Metabolism

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.2022.113130zenodo-depositor-declared
Bioactive terpenoids derived from plant endophytic fungi: An updated review (2011–2020)
inferred← citeshttps://doi.org/10.1002/chin.201529246openalex-snapshot
ChemInform Abstract: Sesquiterpenoids Isolated from an Endophyte Fungus Diaporthe sp.
inferred← citeshttps://doi.org/10.1007/978-981-97-7312-1_10openalex-snapshot
Endophytic Fungal Terpenoids: Biosynthesis and Biological Activity
inferred← citeshttps://doi.org/10.1007/s11101-017-9514-4openalex-snapshot
Endophytic fungi as novel sources of biopesticides: the Macaronesian Laurel forest, a case study
inferred← citeshttps://doi.org/10.1007/s13205-021-02803-xopenalex-snapshot
Cure lies in nature: medicinal plants and endophytic fungi in curbing cancer
inferred← citeshttps://doi.org/10.1007/s13659-026-00651-xopenalex-snapshot
Cytochalasins are a fascinating class of natural compounds: advances in the chemistry, biological activities, mode of action, and structure-activity relationships of novel cytochalasins isolated in the last decade are described
inferred← citeshttps://doi.org/10.1016/b978-0-12-821005-5.00013-2openalex-snapshot
Bioactive natural products of endophytic fungal origin: Production, activity and biotechnology
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.01.029openalex-snapshot
Alkaloids from the mangrove endophytic fungus Diaporthe phaseolorum SKS019
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.07.015openalex-snapshot
Novel natural compounds from endophytic fungi with anticancer activity
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104187openalex-snapshot
Cytochalasins and polyketides from the fungus Diaporthe sp. GZU-1021 and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.10.006openalex-snapshot
Brasilane sesquiterpenoids and dihydrobenzofuran derivatives from Aspergillus terreus [CFCC 81836]
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113357openalex-snapshot
Investigations of specialised metabolites of endophyte Diaporthe destruens hosted in Illigera orbiculata C. Y. Wu
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114357openalex-snapshot
Five brasilane-type sesquiterpenoids with neuroprotective activities from Xylaria nigripes
inferred← citeshttps://doi.org/10.1016/j.phytol.2018.07.011openalex-snapshot
Spirocurvulaide, a novel spirobicyclic polyketide from a marine fungus Curvularia sp. IFB-Z10
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.09.079openalex-snapshot
Antimicrobial and anti-inflammatory compounds from a marine fungus Pleosporales sp.
inferred← citeshttps://doi.org/10.1016/s1875-5364(22)60190-0openalex-snapshot
Drimane-type sesquiterpenoids from fungi
inferred← citeshttps://doi.org/10.1039/c8ra08822eopenalex-snapshot
Potential antihyperlipidemic polyketones from endophytic Diaporthe sp. JC-J7 in Dendrobium nobile
inferred← citeshttps://doi.org/10.1080/10286020.2020.1866560openalex-snapshot
Generation of tryptamine derivatives through biotransformation by Diaporthe sp.
inferred← citeshttps://doi.org/10.1080/14786419.2025.2487687openalex-snapshot
A new insecticidal sesquiterpene from a mangrove endophytic fungus Aspergillus strain sp. GXNU R1
inferred← citeshttps://doi.org/10.3390/cimb47010053openalex-snapshot
Toward an Efficient Differentiation of Two Diaporthe Strains Through Mass Spectrometry for Fungal Biotyping
inferred← citeshttps://doi.org/10.3390/jof9040453openalex-snapshot
Potential of Secondary Metabolites of Diaporthe Species Associated with Terrestrial and Marine Origins
inferred← citeshttps://doi.org/10.3390/md18060321openalex-snapshot
A Review of Terpenes from Marine-Derived Fungi: 2015–2019
inferred← citeshttps://doi.org/10.3390/microorganisms9020217openalex-snapshot
Bioactive Secondary Metabolites of the Genus Diaporthe and Anamorph Phomopsis from Terrestrial and Marine Habitats and Endophytes: 2010–2019
inferred← citeshttps://doi.org/10.3390/molecules24091817openalex-snapshot
Seven New Drimane-Type Sesquiterpenoids from a Marine-Derived Fungus Paraconiothyrium sporulosum YK-03
inferred← citeshttps://doi.org/10.3390/molecules25112485openalex-snapshot
Natural Nitrogenous Sesquiterpenoids and Their Bioactivity: A Review
inferred← citeshttps://doi.org/10.3390/molecules28031175openalex-snapshot
Pioneering Metabolomic Studies on Diaporthe eres Species Complex from Fruit Trees in the South-Eastern Poland
inferred← citeshttps://doi.org/10.4018/979-8-3693-6972-2.ch014openalex-snapshot
Marine World of Terpenes Targeting Specific Cancers
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