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Dimericbiscognienyne A: A Meroterpenoid Dimer from Biscogniauxia sp. with New Skeleton and Its Activity

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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.201510928openalex-snapshot
A Monooxygenase from Boreostereum vibrans Catalyzes Oxidative Decarboxylation in a Divergent Vibralactone Biosynthesis Pathway
inferredcites →https://doi.org/10.1002/mrc.4141openalex-snapshot
3He NMR studies on helium–pyrrole, helium–indole, and helium–carbazole systems: a new tool for following chemistry of heterocyclic compounds
inferredcites →https://doi.org/10.1002/poc.2955openalex-snapshot
Substituent effects on indirect carbon–carbon couplings, J(CC), in substituted thiophenes, pyrroles, and furans studied by experiment and theory
inferredcites →https://doi.org/10.1007/s10600-013-0764-0openalex-snapshot
New Oxirapentyn E from Marine Isolate of the Fungus Isaria felina
inferredcites →https://doi.org/10.1016/0031-9422(96)00106-9openalex-snapshot
Chromanones, benzofurans and other constituents from Ophryosporus lorentzii
inferredcites →https://doi.org/10.1016/j.bmc.2008.04.052openalex-snapshot
Pestaloficiols A–E, bioactive cyclopropane derivatives from the plant endophytic fungus Pestalotiopsis fici
inferredcites →https://doi.org/10.1016/j.bmc.2008.11.066openalex-snapshot
Pestalofones A–E, bioactive cyclohexanone derivatives from the plant endophytic fungus Pestalotiopsis fici
inferredcites →https://doi.org/10.1016/j.fitote.2013.01.010openalex-snapshot
Pestaloficiols Q–S from the plant endophytic fungus Pestalotiopsis fici
inferredcites →https://doi.org/10.1016/j.phytol.2011.12.002openalex-snapshot
Oxirapentyns B–D produced by a marine sediment-derived fungus Isaria felina (DC.) Fr
inferredcites →https://doi.org/10.1016/j.tet.2014.02.060openalex-snapshot
New polyesters from Talaromyces flavus
inferredcites →https://doi.org/10.1016/j.tet.2015.03.033openalex-snapshot
Truncateols A–N, new isoprenylated cyclohexanols from the sponge-associated fungus Truncatella angustata with anti-H1N1 virus activities
inferredcites →https://doi.org/10.1021/acs.jafc.5b05274openalex-snapshot
Lycibarbarspermidines A–O, New Dicaffeoylspermidine Derivatives from Wolfberry, with Activities against Alzheimer’s Disease and Oxidation
inferredcites →https://doi.org/10.1021/ja00105a078openalex-snapshot
Relative and Absolute Stereochemistry of Pyripyropene A, A Potent, Bioavailable Inhibitor of Acyl-CoA:Cholesterol Acyltransferase (ACAT)
inferredcites →https://doi.org/10.1021/ja209809topenalex-snapshot
Two Separate Gene Clusters Encode the Biosynthetic Pathway for the Meroterpenoids Austinol and Dehydroaustinol in Aspergillus nidulans
inferredcites →https://doi.org/10.1021/ja305665fopenalex-snapshot
Merochlorins A–D, Cyclic Meroterpenoid Antibiotics Biosynthesized in Divergent Pathways with Vanadium-Dependent Chloroperoxidases
inferredcites →https://doi.org/10.1021/ja312503yopenalex-snapshot
The Fumagillin Biosynthetic Gene Cluster in Aspergillus fumigatus Encodes a Cryptic Terpene Cyclase Involved in the Formation of β-trans-Bergamotene
inferredcites →https://doi.org/10.1021/ja405518uopenalex-snapshot
Spiro-Ring Formation is Catalyzed by a Multifunctional Dioxygenase in Austinol Biosynthesis
inferredcites →https://doi.org/10.1021/ja408966topenalex-snapshot
A Cytochrome P450 Serves as an Unexpected Terpene Cyclase during Fungal Meroterpenoid Biosynthesis
inferredcites →https://doi.org/10.1021/jacs.5b00570openalex-snapshot
Uncovering the Unusual D-Ring Construction in Terretonin Biosynthesis by Collaboration of a Multifunctional Cytochrome P450 and a Unique Isomerase
inferredcites →https://doi.org/10.1021/jo0349227openalex-snapshot
Synthesis of Anthropomorphic Molecules: The NanoPutians
inferredcites →https://doi.org/10.1021/jo052203hopenalex-snapshot
Chiral Phosphoramide-Catalyzed Enantioselective Addition of Allylic Trichlorosilanes to Aldehydes. Preparative Studies with Bidentate Phosphorus-Based Amides
inferredcites →https://doi.org/10.1021/jo402627sopenalex-snapshot
Analysis of Seven-Membered Lactones by Computational NMR Methods: Proton NMR Chemical Shift Data are More Discriminating than Carbon
inferredcites →https://doi.org/10.1021/np400041yopenalex-snapshot
Xanthoquinodins from the Endolichenic Fungal Strain Chaetomium elatum
inferredcites →https://doi.org/10.1021/np500014mopenalex-snapshot
Oxirapentyns F–K from the Marine-Sediment-Derived Fungus Isaria felina KMM 4639
inferredcites →https://doi.org/10.1021/np500912topenalex-snapshot
Nodulisporiviridins A–H, Bioactive Viridins from Nodulisporium sp.
inferredcites →https://doi.org/10.1021/np700744topenalex-snapshot
Pestalotheols A−D, Bioactive Metabolites from the Plant Endophytic Fungus Pestalotiopsis theae
inferredcites →https://doi.org/10.1021/np900176qopenalex-snapshot
Bioactive Iridoid Glucosides from the Fruit of Gardenia jasminoides
inferredcites →https://doi.org/10.1021/np900308sopenalex-snapshot
Isoprenylated Chromone Derivatives from the Plant Endophytic Fungus Pestalotiopsis fici
inferredcites →https://doi.org/10.1021/ol800136topenalex-snapshot
Chloropupukeananin, the First Chlorinated Pupukeanane Derivative, and Its Precursors from Pestalotiopsis fici
inferredcites →https://doi.org/10.1021/ol901039mopenalex-snapshot
Chloropestolide A, an Antitumor Metabolite with an Unprecedented Spiroketal Skeleton from Pestalotiopsis fici
inferredcites →https://doi.org/10.1039/b602237eopenalex-snapshot
Applications of chiral C3-symmetric molecules
inferredcites →https://doi.org/10.1039/b820413fopenalex-snapshot
Meroterpenoids produced by fungi
inferredcites →https://doi.org/10.1039/c4cc07192aopenalex-snapshot
Structural aesthetics in molecular nanoscience: a unique Ni 26 cluster with a ‘rabbit-face’ topology and a discrete Ni 18 ‘molecular chain’
inferredcites →https://doi.org/10.1039/c4ra02491eopenalex-snapshot
Sporormiellin A, the first tetrahydrofuran-fused furochromone with an unprecedented tetracyclic skeleton from Sporormiella minima
inferredcites →https://doi.org/10.1039/c5cc07141kopenalex-snapshot
Same data, different structures: diastereoisomers with substantially identical NMR data from nature
inferredcites →https://doi.org/10.1039/c5np00090dopenalex-snapshot
Biosynthesis of fungal meroterpenoids
inferredcites →https://doi.org/10.1073/pnas.0400895101openalex-snapshot
Dissecting the pathological effects of human Aβ40 and Aβ42 in Drosophila : A potential model for Alzheimer's disease
inferredcites →https://doi.org/10.1074/jbc.274.49.34916openalex-snapshot
Territrem B, a Tremorgenic Mycotoxin That Inhibits Acetylcholinesterase with a Noncovalent yet Irreversible Binding Mechanism
inferredcites →https://doi.org/10.1248/cpb.49.924openalex-snapshot
New Chroman Derivatives from the Japanese Liverworts Metacalypogeia cordifolia and Cephalozia otaruensis.
inferredcites →https://doi.org/10.5504/bbeq.2012.0101openalex-snapshot
GIAO NMR Calculations of Some Novel 8-Thio-Substituted 1,3,7-Trimethylxanthines: Comparison of Theoretical and Experimental1H Chemical Shifts

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.2022.113124zenodo-depositor-declared
Prenylated cyclohexene-type meroterpenoids and sulfur-containing xanthones produced by Pseudopestalotiopsis theae
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113522zenodo-depositor-declared
Phytotoxic meroterpenoids with herbicidal activities from the phytopathogenic fungus Pseudopestalotiopsis theae
inferred← citeshttps://doi.org/10.2139/ssrn.4806115openalex-extracted
Secondary Metabolites with Anti-Inflammatory Activity from Marine-Derived Fungus Biscogniauxia Sp. 8703
inferred← citeshttps://doi.org/10.1002/ange.202004364openalex-snapshot
Biosynthesis of Biscognienyne B Involving a Cytochrome P450‐Dependent Alkynylation
inferred← citeshttps://doi.org/10.1002/ange.202010528openalex-snapshot
Synthesis of Pyrrolidines by a Csp3‐Csp3/Csp3‐N Transition‐Metal‐Free Domino Reaction of Boronic Acids with γ‐Azido‐N‐Tosylhydrazones
inferred← citeshttps://doi.org/10.1002/ange.202415279openalex-snapshot
Modifications of Prenyl Side Chains in Natural Product Biosynthesis
inferred← citeshttps://doi.org/10.1002/anie.202004364openalex-snapshot
Biosynthesis of Biscognienyne B Involving a Cytochrome P450‐Dependent Alkynylation
inferred← citeshttps://doi.org/10.1002/anie.202010528openalex-snapshot
Synthesis of Pyrrolidines by a Csp3‐Csp3/Csp3‐N Transition‐Metal‐Free Domino Reaction of Boronic Acids with γ‐Azido‐N‐Tosylhydrazones
inferred← citeshttps://doi.org/10.1002/anie.202415279openalex-snapshot
Modifications of Prenyl Side Chains in Natural Product Biosynthesis
inferred← citeshttps://doi.org/10.1002/cbic.202400387openalex-snapshot
Biosynthesis and Assembly Logic of Fungal Hybrid Terpenoid Natural Products
inferred← citeshttps://doi.org/10.1007/s00253-021-11312-zopenalex-snapshot
Peculiarities of meroterpenoids and their bioproduction
inferred← citeshttps://doi.org/10.1007/s12010-023-04328-wopenalex-snapshot
Endophytic Fungus of Achyrocline satureioides: Molecular Identification, Chemical Characterization, and Cytotoxic Evaluation of its Metabolites in Human Melanoma cell line
inferred← citeshttps://doi.org/10.1016/j.apsb.2021.05.001openalex-snapshot
Tripodalsporormielones A–C, unprecedented cage-like polyketides with complex polyvdent bridged and fused ring systems
inferred← citeshttps://doi.org/10.1016/j.apsb.2022.11.023openalex-snapshot
Discovery of a first-in-class ANXA3 degrader for the treatment of triple-negative breast cancer
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106715openalex-snapshot
Anti-inflammatory acetylenic meroterpenoids from the ascidian-derived fungus Amphichorda felina SYSU-MS7908
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107726openalex-snapshot
Identification of three novel P450 enzymes involved in the oxidative modification of a newly discovered fusicoccane diterpene
inferred← citeshttps://doi.org/10.1016/j.cclet.2018.05.019openalex-snapshot
Dimericbiscognienynes B and C: New diisoprenyl-cyclohexene-type meroterpenoid dimers from Biscogniauxia sp.
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112860openalex-snapshot
Meroterpenoids produced by fungi: Occurrence, structural diversity, biological activities, and their molecular targets
inferred← citeshttps://doi.org/10.1016/j.fitote.2017.10.016openalex-snapshot
Phenylisotertronic acids from the TCM endophytic fungus Phyllosticta sp.
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104184openalex-snapshot
New phthalide derivatives from the Biscogniauxia sp. and their activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113955openalex-snapshot
Diisoprenyl-cyclohexene-type meroterpenoids from a mangrove endophytic fungus Aspergillus sp. GXNU-Y65 and their anti-nonalcoholic steatohepatitis activity in AML12 cells
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114857openalex-snapshot
Seven previously undescribed seco-abietane and seco-isopimarane type diterpenoids from Biscogniauxia sp. and their biological activities
inferred← citeshttps://doi.org/10.1016/j.sajb.2020.06.022openalex-snapshot
Biscogniauxia dendrobii sp. nov. and B. petrensis from Dendrobium orchids and the first report of cytotoxicity (towards A549 and K562) of B. petrensis (MFLUCC 14-0151) in vitro
inferred← citeshttps://doi.org/10.1016/j.synbio.2021.02.001openalex-snapshot
Microbial soluble aromatic prenyltransferases for engineered biosynthesis
inferred← citeshttps://doi.org/10.1016/j.tet.2017.09.030openalex-snapshot
Progress in the total synthesis of epoxyquinone natural products: An update
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.09.063openalex-snapshot
Total synthesis of epoxyquinone meroterpenoid natural product biscognienyne B
inferred← citeshttps://doi.org/10.1016/j.tibs.2022.11.002openalex-snapshot
Discovery, biochemical characterization, and bioengineering of cyanobactin prenyltransferases
inferred← citeshttps://doi.org/10.1016/s1875-5364(18)30131-6openalex-snapshot
Advanced natural products chemistry research in China between 2015 and 2017
inferred← citeshttps://doi.org/10.1016/s1875-5364(23)60499-6openalex-snapshot
Thirteen new peptaibols with antimicrobial activities from Trichoderma sp.
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.4c02403openalex-snapshot
Discovery of a Novel 1,4-Benzodiazepine Derivative as a Highly Selective ANXA3 Degrader for the Treatment of Triple-Negative Breast Cancer
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00279openalex-snapshot
Isolation and Structural Characterization of Specific Bacterial β‑Glucuronidase Inhibitors from Noni ( Morinda citrifolia ) Fruits
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00770openalex-snapshot
Total Synthesis of (+)-Pestalofone A and (+)-Iso-A82775C
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00369openalex-snapshot
Diisoprenyl-cyclohexene/ane-Type Meroterpenoids from Biscogniauxia sp. and Their Anti-inflammatory Activities
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04234openalex-snapshot
Biomimetic Total Synthesis of Dispirocochlearoids A–C and Related Ganoderma Meroterpenoid Dimers
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04732openalex-snapshot
Rehmannins A–D, Anti-inflammatory Carotenoid Pigments from the Fresh Root of Rehmannia glutinosa
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00085openalex-snapshot
Enantioselective Total Synthesis of (+)-Iso-A82775C, a Proposed Biosynthetic Precursor of Chloropupukeananin
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00380openalex-snapshot
Total Synthesis of Sinensilactam A
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03025openalex-snapshot
(+)-Dimericbiscognienyne A: Total Synthesis and Mechanistic Investigations of the Key Heterodimerization
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b04019openalex-snapshot
Septosones A–C, in Vivo Anti-inflammatory Meroterpenoids with Rearranged Carbon Skeletons from the Marine Sponge Dysidea septosa
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00454openalex-snapshot
Trematosphones A and B, Two Unique Dimeric Structures from the Desert Plant Endophytic Fungus Trematosphaeria terricola
inferred← citeshttps://doi.org/10.1021/acscentsci.3c01414openalex-snapshot
Discovery of a Potent Antiosteoporotic Drug Molecular Scaffold Derived from Angelica sinensis and Its Bioinspired Total Synthesis
inferred← citeshttps://doi.org/10.1021/acschembio.7b01059openalex-snapshot
Characterization of a Prenyltransferase for Iso-A82775C Biosynthesis and Generation of New Congeners of Chloropestolides
inferred← citeshttps://doi.org/10.1021/acsinfecdis.8b00366openalex-snapshot
Novel Mercapto Propionamide Derivatives with Potent New Delhi Metallo-β-Lactamase-1 Inhibitory Activity and Low Toxicity
inferred← citeshttps://doi.org/10.1021/acsomega.5c12372openalex-snapshot
Meroterpenoids Isolated from Avicennia marina Fruit Fungal Strain Aspergillus sp.
inferred← citeshttps://doi.org/10.1021/acsomega.7b01748openalex-snapshot
Methanolysis of the Cyclic Acetal Function of NanoKid Catalyzed by NanoGoblin, the Pyridinium Salt of Tetracyanocyclopentadienide
inferred← citeshttps://doi.org/10.1038/s41467-018-04298-2openalex-snapshot
Biosynthetic pathway for furanosteroid demethoxyviridin and identification of an unusual pregnane side-chain cleavage
inferred← citeshttps://doi.org/10.1038/s41598-017-13407-yopenalex-snapshot
Phyllomeroterpenoids A-C, Multi-biosynthetic Pathway Derived Meroterpenoids from the TCM Endophytic Fungus Phyllosticta sp. and their Antimicrobial Activities
inferred← citeshttps://doi.org/10.1038/s41929-022-00822-2openalex-snapshot
LimF is a versatile prenyltransferase for histidine-C-geranylation on diverse non-natural substrates
inferred← citeshttps://doi.org/10.1039/c7np90009kopenalex-snapshot
Hot off the press
inferred← citeshttps://doi.org/10.1039/c9np00037bopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c9np00062copenalex-snapshot
Natural disesquiterpenoids: an update
inferred← citeshttps://doi.org/10.1039/d0cb00190bopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d0cc00855aopenalex-snapshot
Sporormielones A–E, bioactive novel C–C coupled orsellinic acid derivative dimers, and their biosynthetic origin
inferred← citeshttps://doi.org/10.1039/d0cc02659jopenalex-snapshot
Advances in catalytic and protecting-group-free total synthesis of natural products: a recent update
inferred← citeshttps://doi.org/10.1039/d0ob02162hopenalex-snapshot
The chemistry and biology of fungal meroterpenoids (2009–2019)
inferred← citeshttps://doi.org/10.1039/d0ob02577aopenalex-snapshot
Nonbiomimetic total synthesis of indole alkaloids using alkyne-based strategies
inferred← citeshttps://doi.org/10.1039/d2nj03531fopenalex-snapshot
Two undescribed pairs of isoprenyl hydroxybenzoic acid derivatives from coculture of Pestalotiopsis sp. and Penicillium bialowiezense : enantioseparation and their absolute configurations
inferred← citeshttps://doi.org/10.1039/d3np00052dopenalex-snapshot
Biosynthesis of fungal terpenoids
inferred← citeshttps://doi.org/10.1039/d3ob00426kopenalex-snapshot
Isolation of new compounds related to xyloketals biosynthesis implies an alternative pathway for furan-fused-chromene formation
inferred← citeshttps://doi.org/10.1039/d3ob01110kopenalex-snapshot
Identification of new bisabosqual-type meroterpenoids reveals non-enzymatic conversion of bisabosquals into seco -bisabosquals
inferred← citeshttps://doi.org/10.1039/d3ob01141kopenalex-snapshot
Natural epoxyquinoids: isolation, biological activity and synthesis. An update
inferred← citeshttps://doi.org/10.1080/10286020.2018.1521804openalex-snapshot
Survey of natural products reported by Asian research groups in 2017
inferred← citeshttps://doi.org/10.1080/10286020.2023.2173180openalex-snapshot
Two new alkaloids from a strain of endophytic fungus Aspergillus sp.
inferred← citeshttps://doi.org/10.1080/10286020.2024.2314188openalex-snapshot
New sesquiterpenoids from Biscogniauxia sp.
inferred← citeshttps://doi.org/10.1080/10286020.2025.2576000openalex-snapshot
Secondary metabolites with anti-inflammatory activity isolated from a marine-derived fungus Biscogniauxia sp. 8703
inferred← citeshttps://doi.org/10.1080/14786419.2019.1610758openalex-snapshot
Spororrminone A and 2-epi-spororrminone A, two new chromones from an endolichenic fungus Sporormiella irregularis
inferred← citeshttps://doi.org/10.1080/14786419.2019.1641807openalex-snapshot
Cladosporine A, a new indole diterpenoid alkaloid with antimicrobial activities from Cladosporium sp.
inferred← citeshttps://doi.org/10.1080/14786419.2024.2303601openalex-snapshot
Cytotoxic metabolites from the mangrove endophytic fungus Aspergillus sp. GXNU QG1a
inferred← citeshttps://doi.org/10.1080/14786419.2024.2390614openalex-snapshot
A new isoprenyl-phenol-type meroterpenoid from mangrove endophytic fungus Aspergillus sp. GXNU-Y65
inferred← citeshttps://doi.org/10.1093/jimb/kuaf035openalex-snapshot
Mapping epoxyquinoid biosynthesis: Enzyme functions across bacteria and fungi
inferred← citeshttps://doi.org/10.2174/0929867326666190618113613openalex-snapshot
Natural Products as Potential Anti-Alzheimer Agents
inferred← citeshttps://doi.org/10.3389/fchem.2021.749272openalex-snapshot
Two New Diterpenoids from Biscogniauxia sp. and Their Activities
inferred← citeshttps://doi.org/10.3389/fphar.2025.1584962openalex-snapshot
Research progress on heteroterpene and meroterpenoid compounds from the Rhododendron genus and their NMR characterization and biological activity
inferred← citeshttps://doi.org/10.3390/ijms23073686openalex-snapshot
Combination Strategy of Genetic Dereplication and Manipulation of Epigenetic Regulators Reveals a Novel Compound from Plant Endophytic Fungus
inferred← citeshttps://doi.org/10.3390/ijms241311184openalex-snapshot
Fungal BGCs for Production of Secondary Metabolites: Main Types, Central Roles in Strain Improvement, and Regulation According to the Piano Principle
inferred← citeshttps://doi.org/10.3390/md15060153openalex-snapshot
Chalcomycins from Marine-Derived Streptomyces sp. and Their Antimicrobial Activities
inferred← citeshttps://doi.org/10.3390/md22020058openalex-snapshot
Diisoprenyl Cyclohexene-Type Meroterpenoids with Cytotoxic Activity from a Mangrove Endophytic Fungus Aspergillus sp. GXNU-Y85
inferred← citeshttps://doi.org/10.3390/molecules24203778openalex-snapshot
An Overview of Saturated Cyclic Ethers: Biological Profiles and Synthetic Strategies
inferred← citeshttps://doi.org/10.3390/org3030023openalex-snapshot
Total Syntheses of Chloropupukeananin and Its Related Natural Products
inferred← citeshttps://doi.org/10.3390/toxins15120686openalex-snapshot
Secondary Metabolites of Biscogniauxia: Distribution, Chemical Diversity, Bioactivity, and Implications of the Occurrence
inferred← citeshttps://doi.org/10.7717/peerj.15461openalex-snapshot
Endophytic fungus Biscogniauxia petrensis produces antibacterial substances
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