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Bipolarolides A–G: Ophiobolin‐Derived Sesterterpenes with Three New Carbon Skeletons from Bipolaris sp. TJ403‐B1
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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/ange.201509263openalex-snapshot
An Unusual Chimeric Diterpene Synthase from Emericella variecolor and Its Functional Conversion into a Sesterterpene Synthase by Domain Swapping
inferredcites →https://doi.org/10.1002/ange.201601448openalex-snapshot
Astellifadiene: Structure Determination by NMR Spectroscopy and Crystalline Sponge Method, and Elucidation of its Biosynthesis
inferredcites →https://doi.org/10.1002/ange.201701879openalex-snapshot
Total Syntheses of Sesterterpenoid Ansellones A and B, and Phorbadione
inferredcites →https://doi.org/10.1002/ange.201704628openalex-snapshot
Unified Asymmetric Total Syntheses of (−)‐Alotaketals A–D and (−)‐Phorbaketal A
inferredcites →https://doi.org/10.1002/ange.201711444openalex-snapshot
Diverged Plant Terpene Synthases Reroute the Carbocation Cyclization Path towards the Formation of Unprecedented 6/11/5 and 6/6/7/5 Sesterterpene Scaffolds
inferredcites →https://doi.org/10.1002/anie.201509263openalex-snapshot
An Unusual Chimeric Diterpene Synthase from Emericella variecolor and Its Functional Conversion into a Sesterterpene Synthase by Domain Swapping
inferredcites →https://doi.org/10.1002/anie.201601448openalex-snapshot
Astellifadiene: Structure Determination by NMR Spectroscopy and Crystalline Sponge Method, and Elucidation of its Biosynthesis
inferredcites →https://doi.org/10.1002/anie.201701879openalex-snapshot
Total Syntheses of Sesterterpenoid Ansellones A and B, and Phorbadione
inferredcites →https://doi.org/10.1002/anie.201704628openalex-snapshot
Unified Asymmetric Total Syntheses of (−)‐Alotaketals A–D and (−)‐Phorbaketal A
inferredcites →https://doi.org/10.1002/anie.201711444openalex-snapshot
Diverged Plant Terpene Synthases Reroute the Carbocation Cyclization Path towards the Formation of Unprecedented 6/11/5 and 6/6/7/5 Sesterterpene Scaffolds
inferredcites →https://doi.org/10.1002/chem.201204119openalex-snapshot
Enantioselective Total Synthesis of (+)‐Ophiobolin A
inferredcites →https://doi.org/10.1016/j.bmcl.2013.04.034openalex-snapshot
3-Anhydro-6-hydroxy-ophiobolin A, a new sesterterpene inhibiting the growth of methicillin-resistant Staphylococcus aureus and inducing the cell death by apoptosis on K562, from the phytopathogenic fungus Bipolaris oryzae
inferredcites →https://doi.org/10.1021/acs.orglett.5b02404openalex-snapshot
Molecular Basis for Stellatic Acid Biosynthesis: A Genome Mining Approach for Discovery of Sesterterpene Synthases
inferredcites →https://doi.org/10.1021/acs.orglett.6b00552openalex-snapshot
Multiple Oxidative Modifications in the Ophiobolin Biosynthesis: P450 Oxidations Found in Genome Mining
inferredcites →https://doi.org/10.1021/acs.orglett.6b03557openalex-snapshot
Phomopsterones A and B, Two Functionalized Ergostane-Type Steroids from the Endophytic Fungus Phomopsis sp. TJ507A
inferredcites →https://doi.org/10.1021/acs.orglett.8b02137openalex-snapshot
Fusicoccane-Derived Diterpenoids from Alternaria brassicicola: Investigation of the Structure–Stability Relationship and Discovery of an IKKβ Inhibitor
inferredcites →https://doi.org/10.1021/acs.orglett.8b02534openalex-snapshot
Peniroquesines A–C: Sesterterpenoids Possessing a 5–6–5–6–5-Fused Pentacyclic Ring System from Penicillium roqueforti YJ-14
inferredcites →https://doi.org/10.1021/acs.orglett.8b03553openalex-snapshot
Alterbrassicicene A, a Highly Transformed Fusicoccane-Derived Diterpenoid with Potent PPAR-γ Agonistic Activity from Alternaria brassicicola
inferredcites →https://doi.org/10.1021/acs.orglett.9b00581openalex-snapshot
Niduterpenoids A and B: Two Sesterterpenoids with a Highly Congested Hexacyclic 5/5/5/5/3/5 Ring System from the Fungus Aspergillus nidulans
inferredcites →https://doi.org/10.1021/jacs.5b08319openalex-snapshot
Genome Mining for Sesterterpenes Using Bifunctional Terpene Synthases Reveals a Unified Intermediate of Di/Sesterterpenes
inferredcites →https://doi.org/10.1021/jacs.6b05799openalex-snapshot
Genome-Based Discovery of an Unprecedented Cyclization Mode in Fungal Sesterterpenoid Biosynthesis
inferredcites →https://doi.org/10.1021/jo00245a008openalex-snapshot
Some new phytotoxic ophiobolins produced by Drechslera oryzae
inferredcites →https://doi.org/10.1021/ol303408aopenalex-snapshot
Identification of Ophiobolin F Synthase by a Genome Mining Approach: A Sesterterpene Synthase from Aspergillus clavatus
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.2021.112910zenodo-depositor-declared
Spectanoids A−H: Eight undescribed sesterterpenoids from Aspergillus spectabilis
inferred← citeshttps://doi.org/10.1002/ajoc.202500116openalex-snapshot
Recent Developments in Prins Cyclization Toward the Synthesis of Spirocyclic Scaffolds
inferred← citeshttps://doi.org/10.1002/ange.202003643openalex-snapshot
Complex Polypropionates from a South China Sea Photosynthetic Mollusk: Isolation and Biomimetic Synthesis Highlighting Novel Rearrangements
inferred← citeshttps://doi.org/10.1002/ange.202004177openalex-snapshot
A Concise Total Synthesis of (+)‐Waihoensene Guided by Quaternary Center Analysis
inferred← citeshttps://doi.org/10.1002/ange.202319306openalex-snapshot
Bioinspired Total Synthesis of Bipolarolides A and B
inferred← citeshttps://doi.org/10.1002/ange.202422615openalex-snapshot
Total Synthesis of Lugdunomycin via Sequential Photoinduced Spiroketalization and Isobenzofuran Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1002/anie.202003643openalex-snapshot
Complex Polypropionates from a South China Sea Photosynthetic Mollusk: Isolation and Biomimetic Synthesis Highlighting Novel Rearrangements
inferred← citeshttps://doi.org/10.1002/anie.202004177openalex-snapshot
A Concise Total Synthesis of (+)‐Waihoensene Guided by Quaternary Center Analysis
inferred← citeshttps://doi.org/10.1002/anie.202319306openalex-snapshot
Bioinspired Total Synthesis of Bipolarolides A and B
inferred← citeshttps://doi.org/10.1002/anie.202422615openalex-snapshot
Total Synthesis of Lugdunomycin via Sequential Photoinduced Spiroketalization and Isobenzofuran Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1007/s13659-024-00486-4openalex-snapshot
Unveiling the mechanism of action of a novel natural dual inhibitor of SARS-CoV-2 Mpro and PLpro with molecular dynamics simulations
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Undulanoids A−D: Unexpected sesterterpenoids as potent S100A8/A9 complex inhibitors for psoriasis treatment
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106106openalex-snapshot
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Distachydrimanes A–F, phenylspirodrimane dimers and hybrids with cytotoxic activity from the coral-derived fungus Stachybotrys chartarum
inferred← citeshttps://doi.org/10.1016/j.cclet.2025.110904openalex-snapshot
Ophiobolin-type sesterterpenoids with unprecedented chemical architectures from Bipolaris oryzae and their inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114117openalex-snapshot
Natural products from mangrove sediments-derived microbes: Structural diversity, bioactivities, biosynthesis, and total synthesis
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.145144openalex-snapshot
New antibacterial polyketides from the plant endophytic f ungi Talaromyces pinophilus AF-02 and their molecular modelling studies
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112374openalex-snapshot
Structurally diverse and bioactive alkaloids from an insect-derived fungus Neosartorya fischeri
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112762openalex-snapshot
Bioactive sesterterpenoids from the fungus Penicillium roqueforti YJ-14
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114116openalex-snapshot
WITHDRAWN: Alkaloid constituents from Anacyclus pyrethrum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114255openalex-snapshot
Alkaloids from Anacyclus pyrethrum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114802openalex-snapshot
1H NMR-guided isolation of ophiobolins from Bipolaris maydis and their bioactivities
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153869openalex-snapshot
Ancepsone A, a new cheilanthane sesterterpene from Aleuritopteris anceps
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154303openalex-snapshot
Novel indole alkaloids from Rauvolfia yunnanensis, inhibiting ESBL producing Escherichia coli by targeting cell membrane integrity
inferred← citeshttps://doi.org/10.1016/s1875-5364(19)30116-5openalex-snapshot
Bipolarins A–H, eight new ophiobolin-type sesterterpenes with antimicrobial activity from fungus Bipolaris sp. TJ403-B1
inferred← citeshttps://doi.org/10.1016/s1875-5364(24)60629-1openalex-snapshot
New pimarane diterpenoids with antibacterial activity from fungus Arthrinium sp. ZS03
inferred← citeshttps://doi.org/10.1021/acs.accounts.4c00654openalex-snapshot
Bioinspired Total Synthesis of Natural Products
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c08134openalex-snapshot
Bipoladien A, a Sesterterpenoid Containing an Undescribed 5/8/5/7 Carbon Skeleton from Bipolaris maydis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00165openalex-snapshot
Modified Fusicoccane-Type Diterpenoids from Alternaria brassicicola
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00298openalex-snapshot
Proversilins A–E, Drimane-Type Sesquiterpenoids from the Endophytic Aspergillus versicolor
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00327openalex-snapshot
Bipolaquinones A–J, Immunosuppressive Meroterpenoids from a Soil-Derived Bipolaris zeicola
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00385openalex-snapshot
Undobolins A–L, Ophiobolin-Type Sesterterpenoids from Aspergillus undulatus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00658openalex-snapshot
Maydisens, Sesterterpenoids with Anti-MDR Activity from Bipolaris maydis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c01105openalex-snapshot
Metabolomics-Guided Discovery of Bipolarolides H–O, New Ophiobolin-Type Sesterterpenes with Antibacterial Activity from the Marine-Derived Fungus Uzbekistanica storfjordensis sp. nov.
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00024openalex-snapshot
Bipoladisins A–G, Uncommon Sesterterpenoids with Three Types of Carbon Skeletons from Bipolaris maydis and Their Reversal Activity on Paclitaxel Resistance
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00744openalex-snapshot
Bipolaricins A–I, Ophiobolin-Type Tetracyclic Sesterterpenes from a Phytopathogenic Bipolaris sp. Fungus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b01000openalex-snapshot
Reisolation and Configurational Reinvestigation of Cottoquinazolines E–G from an Arthropod-Derived Strain of the Fungus Neosartorya fischeri
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01127openalex-snapshot
Catalyst-free Tandem 1,3-Dipolar Cycloaddition/Aldol Condensation: Diastereoselective Construction of the Azatetraquinane Skeleton
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02237openalex-snapshot
Bioactive Polyketide-Terpenoid Hybrids from a Soil-Derived Fungus Bipolaris zeicola
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02572openalex-snapshot
A Molecular Iodine-Mediated Synthesis of Cyclopenta[c]furo[3,2-b]furan-5,6-diones: Assembly of an Angular Dioxatriquinane Core
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00055openalex-snapshot
Antimicrobial Activities of Ophiobolins from Bipolaris maydis against Foodborne Pathogenic Bacteria via Biofilm Formation Inhibition
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00291openalex-snapshot
Asperiecolins A–D: Undescribed Variecolin-Type Sesterterpenoids with Anti-Inflammatory and AChE Inhibitory Activities from Aspergillus sp. TJ403-YJ22
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00284openalex-snapshot
Spectaterpenoids A–G, Sesterterpenoids with Unprecedented Polycyclic Ring System from Aspergillus spectabilis
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03270openalex-snapshot
Periconiastone A, an Antibacterial Ergosterol with a Pentacyclo[8.7.0.01,5.02,14.010,15]heptadecane System from Periconia sp. TJ403-rc01
inferred← citeshttps://doi.org/10.1021/jacs.4c04059openalex-snapshot
Concise Total Synthesis of (−)-Bipolarolide D
inferred← citeshttps://doi.org/10.1021/jacs.5c09835openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacsau.4c00680openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d0np00069hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d0np00070aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d0qo00301hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d1qo01302eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d2gc02058kopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d2qo00983hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d3np00035dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d3sc04238copenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d4np00041bopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d4qo02057jopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d5ra09257dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1055/s-0040-1705953openalex-snapshot
Synthesis of Cyclohexane-Angularly-Fused Triquinanes
inferred← citeshttps://doi.org/10.1080/10286020.2020.1844675openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/10286020.2021.1946042openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/14786419.2020.1789638openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/14786419.2020.1858409openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/14786419.2022.2150846openalex-snapshot
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inferred← citeshttps://doi.org/10.1515/9783111850825-019openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fmicb.2020.00856openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fmicb.2022.916418openalex-snapshot
Soil Microbial Communities Affect the Growth and Secondary Metabolite Accumulation in Bletilla striata (Thunb.) Rchb. f.
inferred← citeshttps://doi.org/10.3390/ijms23031903openalex-snapshot
The Biosynthesis and Transport of Ophiobolins in Aspergillus ustus 094102
inferred← citeshttps://doi.org/10.3390/jof8101080openalex-snapshot
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inferred← citeshttps://doi.org/10.6023/a26050154openalex-snapshot
Advances in the Application of Mizoroki-Heck Reaction in Natural Product Synthesis ★
inferred← citeshttps://doi.org/10.6023/cjoc202408029openalex-snapshot
Advances in the Total Syntheses of Tetraquinane and Tetraquinane-Type Terpenes
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