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Septosones A–C, in Vivo Anti-inflammatory Meroterpenoids with Rearranged Carbon Skeletons from the Marine Sponge Dysidea septosa
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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.201611617openalex-snapshot
Cyanobacterial ent‐Sterol‐Like Natural Products from a Deviated Ubiquinone Pathway
inferredcites →https://doi.org/10.1002/chem.201304809openalex-snapshot
Enantioselective Total Synthesis of Dysidavarone A, a Novel Sesquiterpenoid Quinone from the Marine Sponge Dysidea avara
inferredcites →https://doi.org/10.1002/chem.201702336openalex-snapshot
An Unprecedented Blue Chromophore Found in Nature using a “Chemistry First” and Molecular Networking Approach: Discovery of Dactylocyanines A–H
inferredcites →https://doi.org/10.1002/jat.3303openalex-snapshot
Copper toxicology, oxidative stress and inflammation using zebrafish as experimental model
inferredcites →https://doi.org/10.1016/j.fsi.2018.09.032openalex-snapshot
Tenacissoside H exerts an anti-inflammatory effect by regulating the nf-κb and p38 pathways in zebrafish
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00867openalex-snapshot
Meroterpenoids from a Tropical Dysidea sp. Sponge
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00367openalex-snapshot
Sesquiterpene Hydroquinones with Protein Tyrosine Phosphatase 1B Inhibitory Activities from a Dysidea sp. Marine Sponge Collected in Okinawa
inferredcites →https://doi.org/10.1021/acs.orglett.6b03264openalex-snapshot
Dimericbiscognienyne A: A Meroterpenoid Dimer from Biscogniauxia sp. with New Skeleton and Its Activity
inferredcites →https://doi.org/10.1021/acs.orglett.8b00327openalex-snapshot
Simpterpenoid A, a Meroterpenoid with a Highly Functionalized Cyclohexadiene Moiety Featuring gem-Propane-1,2-dione and Methylformate Groups, from the Mangrove-Derived Penicillium simplicissimum MA-332
inferredcites →https://doi.org/10.1021/acs.orglett.8b00584openalex-snapshot
Griseofamines A and B: Two Indole-Tetramic Acid Alkaloids with 6/5/6/5 and 6/5/7/5 Ring Systems from Penicillium griseofulvum
inferredcites →https://doi.org/10.1021/acs.orglett.8b01148openalex-snapshot
Dysiarenone, a Dimeric C21 Meroterpenoid with Inhibition of COX-2 Expression from the Marine Sponge Dysidea arenaria
inferredcites →https://doi.org/10.1021/jo981037topenalex-snapshot
Bolinaquinone: A Novel Cytotoxic Sesquiterpene Hydroxyquinone from a Philippine Dysidea Sponge
inferredcites →https://doi.org/10.1021/np040237zopenalex-snapshot
Merosesquiterpenes from Two Sponges of the Genus Dysidea
inferredcites →https://doi.org/10.1021/np050171nopenalex-snapshot
Anti-inflammatory Sesquiterpene-quinones from the New Zealand Sponge Dysidea cf. cristagalli
inferredcites →https://doi.org/10.1021/np070600copenalex-snapshot
Sesquiterpene Quinones and Related Metabolites from Phyllosticta spinarum, a Fungal Strain Endophytic in Platycladus orientalis of the Sonoran Desert
inferredcites →https://doi.org/10.1021/np1000285openalex-snapshot
Sesquiterpenoid Aminoquinones from the Marine Sponge Dysidea sp.
inferredcites →https://doi.org/10.1021/np400633mopenalex-snapshot
Cytotoxic and Protein Kinase Inhibiting Nakijiquinones and Nakijiquinols from the Sponge Dactylospongia metachromia
inferredcites →https://doi.org/10.1021/np500793gopenalex-snapshot
Puupehenol, a Potent Antioxidant Antimicrobial Meroterpenoid from a Hawaiian Deep-Water Dactylospongia sp. Sponge
inferredcites →https://doi.org/10.1021/np500843mopenalex-snapshot
Cytotoxic Activity of Rearranged Drimane Meroterpenoids against Colon Cancer Cells via Down-Regulation of β-Catenin Expression
inferredcites →https://doi.org/10.1021/np50089a012openalex-snapshot
5-epi-Isospongiaquinone, a New Sesquiterpene/Quinone Antibiotic from an Australian Marine Sponge, Spongia hispida
inferredcites →https://doi.org/10.1021/np8002035openalex-snapshot
Sesquiterpenes from the Hainan Sponge Dysidea septosa
inferredcites →https://doi.org/10.1021/ol061333popenalex-snapshot
Avinosol, A Meroterpenoid-Nucleoside Conjugate with Antiinvasion Activity Isolated from the Marine Sponge Dysidea sp.
inferredcites →https://doi.org/10.1021/ol202994copenalex-snapshot
Dysidavarones A–D, New Sesquiterpene Quinones from the Marine Sponge Dysidea avara
inferredcites →https://doi.org/10.1021/ol400156uopenalex-snapshot
Total Synthesis and Antibacterial Activity of Dysidavarone A
inferredcites →https://doi.org/10.1038/aps.2013.2openalex-snapshot
Characterization of a novel curcumin analog P1 as potent inhibitor of the NF-κB signaling pathway with distinct mechanisms
inferredcites →https://doi.org/10.1038/nrd4627openalex-snapshot
Zebrafish as tools for drug discovery
inferredcites →https://doi.org/10.1097/00001813-200404000-00009openalex-snapshot
Smenospongine, a spongean sesquiterpene aminoquinone, induces erythroid differentiation in K562 cells
inferredcites →https://doi.org/10.2174/157019310791384128openalex-snapshot
Quinone/Hydroquinone Sesquiterpenes
inferredcites →https://doi.org/10.3390/md9020154openalex-snapshot
Antiproliferative and Antiangiogenic Activities of Smenospongine, a Marine Sponge Sesquiterpene Aminoquinone
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.2022.113578zenodo-depositor-declared
Sarcoelegans A–H, eight undescribed cembranes with anti-inflammatory and anti-thrombotic activities from the South China Sea soft coral Sarcophyton elegans
inferred← citeshttps://doi.org/10.1002/adsc.202201030openalex-snapshot
An Acid Promoted, Domino Approach for the Selective Synthesis of Spirocyclic Systems#
inferred← citeshttps://doi.org/10.1002/ange.201909557openalex-snapshot
Palladium‐Catalyzed [2+2+1] Spiroannulation via Alkyne‐Directed Remote C−H Arylation and Subsequent Arene Dearomatization
inferred← citeshttps://doi.org/10.1002/ange.202218085openalex-snapshot
Somalactams A–D: Anti‐inflammatory Macrolide Lactams with Unique Ring Systems from an Arctic Actinomycete Strain
inferred← citeshttps://doi.org/10.1002/ange.202415249openalex-snapshot
Formation of Multiple Naturally Occurring Meroterpenoid Scaffolds by the Norrish‐Yang Reaction of a p ‐Benzoquinone
inferred← citeshttps://doi.org/10.1002/ange.202505270openalex-snapshot
Total Synthesis of Dactyloquinone A and Spiroetherone A via a Metal‐Hydride Hydrogen Atom Transfer (MHAT) Process and a Quinol–Enedione Rearrangement
inferred← citeshttps://doi.org/10.1002/anie.201909557openalex-snapshot
Palladium‐Catalyzed [2+2+1] Spiroannulation via Alkyne‐Directed Remote C−H Arylation and Subsequent Arene Dearomatization
inferred← citeshttps://doi.org/10.1002/anie.202218085openalex-snapshot
Somalactams A–D: Anti‐inflammatory Macrolide Lactams with Unique Ring Systems from an Arctic Actinomycete Strain
inferred← citeshttps://doi.org/10.1002/anie.202415249openalex-snapshot
Formation of Multiple Naturally Occurring Meroterpenoid Scaffolds by the Norrish‐Yang Reaction of a p ‐Benzoquinone
inferred← citeshttps://doi.org/10.1002/anie.202505270openalex-snapshot
Total Synthesis of Dactyloquinone A and Spiroetherone A via a Metal‐Hydride Hydrogen Atom Transfer (MHAT) Process and a Quinol–Enedione Rearrangement
inferred← citeshttps://doi.org/10.1002/cbdv.202100578openalex-snapshot
New NF‐κB Inhibitory Steroids from the Marine Sponge Dysidea avara Collected from the South China Sea
inferred← citeshttps://doi.org/10.1002/ceur.70350openalex-snapshot
Diversification of the Avarane Skeleton Toward Spiroetherone A
inferred← citeshttps://doi.org/10.1002/cjoc.202200129openalex-snapshot
Structural and Biological Insights into the Hot‐Spot Marine Natural Products Reported from 2012 to 2021
inferred← citeshttps://doi.org/10.1002/cjoc.70121openalex-snapshot
Total Synthesis of 1'‐epi‐Septosones B and C and Discovery of Novel Compounds with Anti‐Cancer Activity
inferred← citeshttps://doi.org/10.1007/s11426-024-2211-yopenalex-snapshot
Tandem asymmetric dearomatized functionalization reaction of phenols with Evans-ynamides enabled by divergent electrophiles
inferred← citeshttps://doi.org/10.1007/s12010-026-05684-zopenalex-snapshot
Analysis of the Anti-inflammatory Effects of a Delivery System Based on Alginate Hydrogels Enriched with Bioactive Compounds from Marine Sponge Dysidea robusta
inferred← citeshttps://doi.org/10.1007/s42995-019-00021-2openalex-snapshot
Metabolites from marine invertebrates and their symbiotic microorganisms: molecular diversity discovery, mining, and application
inferred← citeshttps://doi.org/10.1016/b978-0-443-29190-6.10015-7openalex-snapshot
Impacts on noninfectious diseases
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103226openalex-snapshot
Chemical constituents from Alismatis Rhizoma and their anti-inflammatory activities in vitro and in vivo
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103435openalex-snapshot
Discovery of nitrogenous sesquiterpene quinone derivatives from sponge Dysidea septosa with anti-inflammatory activity in vivo zebrafish model
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e35974openalex-snapshot
Metabolomics-based profiling of anti-inflammatory compounds from Mentha spicata in shanghe, China
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113640openalex-snapshot
Steroidal alkaloids from the bulbs of Fritillaria unibracteata var. wabuensis and their anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113702openalex-snapshot
Pallamins A–C, ent-labdane and pallavicinin based dimers from the Chinese liverwort Pallavicinia ambigua (mitt.) stephani
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152715openalex-snapshot
(±)-Pabmaragramin, a scalemic meroterpenoid produced by Marasmius graminum via precursor-assisted biosynthesis
inferred← citeshttps://doi.org/10.1016/s1875-5364(22)60161-4openalex-snapshot
Dysideanones F—G and dysiherbols D—E, unusual sesquiterpene quinones with rearranged skeletons from the marine sponge Dysidea avara
inferred← citeshttps://doi.org/10.1016/s1875-5364(26)61202-2openalex-snapshot
“Marine Rule”: discovery of marine natural small molecule drug leads in China in the past decade
inferred← citeshttps://doi.org/10.1021/acs.jafc.9b06132openalex-snapshot
Lipid Fingerprinting of Different Material Sources by UPLC-Q-Exactive Orbitrap/MS Approach and Their Zebrafish-Based Activities Comparison
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00828openalex-snapshot
Rapid Approaches for Assignment of the Relative Configuration in 1-Oxygenated 1,2-Diarylpropan-3-ols by 1H NMR Spectroscopy
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00964openalex-snapshot
Pinguisane Sesquiterpenoids from the Chinese Liverwort Trocholejeunea sandvicensis and Their Anti-Inflammatory Activity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00877openalex-snapshot
Pseudoceranoids A–J, Sesquiterpene-Based Meroterpenoids with Cytotoxicity from the Sponge Pseudoceratina purpurea
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c01293openalex-snapshot
Cinerols L–R, Anti-inflammatory Meroterpenoids from the Marine Sponge Dysidea cinerea
inferred← citeshttps://doi.org/10.1021/acs.jpca.4c04423openalex-snapshot
DFT Investigation on Palladium-Catalyzed [2 + 2 + 1] Spiroannulation between Aryl Halides and Alkynes: Mechanism, Base Additive Role, and Solvent and Ligand Effects
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02772openalex-snapshot
Sinunanolobatone A, an Anti-inflammatory Diterpenoid with Bicyclo[13.1.0]pentadecane Carbon Scaffold, and Related Casbanes from the Sanya Soft Coral Sinularia nanolobata
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02409openalex-snapshot
Dysambiol, an Anti-inflammatory Secomeroterpenoid from a Dysidea sp. Marine Sponge
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03867openalex-snapshot
Herqupenoid A, an Unparalleled Sesquiterpene-Quinone Hybrid Featuring a Multicyclic Caged 2,7-Dioxatetracyclo[5.4.0.04,11.05,9]Hendecane Fragment from Penicillium herquei
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03236openalex-snapshot
Asymmetric Total Synthesis of Leptosphin C
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02635openalex-snapshot
Chiral Phosphoric Acid-Catalyzed Enantioselective Dearomative Spirocyclization of Phenol-Ynamides by Kinetic Resolution
inferred← citeshttps://doi.org/10.1021/acsomega.4c02488openalex-snapshot
Marchaetoglobins A–D: Four Cytochalasans with Proangiogenic Activity from the Marine-Sponge-Associated Fungus Chaetomium globosum 162105
inferred← citeshttps://doi.org/10.1021/jacs.2c08435openalex-snapshot
Enantioselective Total Synthesis of Dysiherbols A, C, and D
inferred← citeshttps://doi.org/10.1039/c9qo01346fopenalex-snapshot
Spiroetherones A and B, sesquiterpene naphthoquinones, as angiogenesis inhibitors from the marine sponge Dysidea etheria
inferred← citeshttps://doi.org/10.1039/d0ob01985bopenalex-snapshot
Structural elucidation, total synthesis, and cytotoxic activity of effphenol A
inferred← citeshttps://doi.org/10.1039/d1cc05253eopenalex-snapshot
TfOH catalysed domino-double annulation of arenes with propargylic alcohols: a unified approach to indene polycyclic systems
inferred← citeshttps://doi.org/10.1039/d1fo00796copenalex-snapshot
Characterization and bioactivities of phospholipids from squid viscera and gonads using ultra-performance liquid chromatography-Q-exactive orbitrap/mass spectrometry-based lipidomics and zebrafish models
inferred← citeshttps://doi.org/10.1039/d2np00045hopenalex-snapshot
Natural sesquiterpene quinone/quinols: chemistry, biological activity, and synthesis
inferred← citeshttps://doi.org/10.1039/d3gc03222aopenalex-snapshot
Chiral Brønsted acid-catalyzed asymmetric dearomative spirocyclization of alkynyl thioethers
inferred← citeshttps://doi.org/10.1055/a-1546-2572openalex-snapshot
Bioinspired Total Synthesis of Marine Anticancer Meroterpenoids Dysideanone B and Dysiherbol A and Structure Revision of Dysiherbol A
inferred← citeshttps://doi.org/10.1080/10286020.2020.1844675openalex-snapshot
Survey of natural products reported by Asian research groups in 2019
inferred← citeshttps://doi.org/10.1111/1750-3841.15834openalex-snapshot
Anti‐inflammatory peptides and metabolomics‐driven biomarkers discovery from sea cucumber protein hydrolysates
inferred← citeshttps://doi.org/10.3389/fmars.2026.1774652openalex-snapshot
Therapeutic potential of marine sponge–derived bioactive compounds: a review
inferred← citeshttps://doi.org/10.3389/fphar.2022.830103openalex-snapshot
Biological activities of meroterpenoids isolated from different sources
inferred← citeshttps://doi.org/10.3390/biom11070957openalex-snapshot
Meroterpenoids: A Comprehensive Update Insight on Structural Diversity and Biology
inferred← citeshttps://doi.org/10.3390/cimb47020096openalex-snapshot
Meroterpenoids from Terrestrial and Marine Fungi: Promising Agents for Neurodegenerative Disorders—An Updated Review
inferred← citeshttps://doi.org/10.3390/md19010038openalex-snapshot
An Anti-Inflammatory 2,4-Cyclized-3,4-Secospongian Diterpenoid and Furanoterpene-Related Metabolites of a Marine Sponge Spongia sp. from the Red Sea
inferred← citeshttps://doi.org/10.3390/md19100572openalex-snapshot
Research Progress in Anti-Inflammatory Bioactive Substances Derived from Marine Microorganisms, Sponges, Algae, and Corals
inferred← citeshttps://doi.org/10.3390/md20090574openalex-snapshot
Sarcoeleganolides C–G, Five New Cembranes from the South China Sea Soft Coral Sarcophyton elegans
inferred← citeshttps://doi.org/10.3390/md22040183openalex-snapshot
Meroterpenoids from Marine Sponge Hyrtios sp. and Their Anticancer Activity against Human Colorectal Cancer Cells
inferred← citeshttps://doi.org/10.3390/md22120540openalex-snapshot
Recent Advances of the Zebrafish Model in the Discovery of Marine Bioactive Molecules
inferred← citeshttps://doi.org/10.3390/md23030096openalex-snapshot
Bioactive Terpenes from Marine Sponges and Their Associated Organisms
inferred← citeshttps://doi.org/10.3390/molecules27020350openalex-snapshot
Lipid Profiles of the Heads of Four Shrimp Species by UPLC–Q–Exactive Orbitrap/MS and Their Cardiovascular Activities
inferred← citeshttps://doi.org/10.3762/bjoc.21.177openalex-snapshot
Recent advances in Norrish–Yang cyclization and dicarbonyl photoredox reactions for natural product synthesis
inferred← citeshttps://doi.org/10.52547/ismj.24.4.341openalex-snapshot
Sea God- Sponges: Toxins and Secondary Metabolites
inferred← citeshttps://doi.org/10.70675/91fc8a0ez46d2z4b01zb79cz8eca9cab1d5bopenalex-snapshot
Stratégies de synthèse de sesquiterpènes quinones/hydroquinones : synthèse totale de la dactyloquinone A et de la structure proposée de la spiroetherone A
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