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Anti-inflammatory Sesquiterpene-quinones from the New Zealand Sponge Dysidea cf. cristagalli
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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/jcp.1041630306openalex-snapshot
Evidence that cell survival is controlled by interleukin‐3 independently of cell proliferation
inferredcites →https://doi.org/10.1016/0014-2999(94)90759-5openalex-snapshot
Avarol and avarone, two new anti-inflammatory agents of marine origin
inferredcites →https://doi.org/10.1016/s0040-4020(01)90094-8openalex-snapshot
Further bioactive derivative of avarol from Dysidea avara
inferredcites →https://doi.org/10.1021/np040237zopenalex-snapshot
Merosesquiterpenes from Two Sponges of the Genus Dysidea
inferredcites →https://doi.org/10.1021/np50073a005openalex-snapshot
New Avarone and Avarol Derivatives from the Marine Sponge Dysidea cinerea
inferredcites →https://doi.org/10.1021/np50100a007openalex-snapshot
Defensive Secretion of the Millipede Floridobolus penneri
inferredcites →https://doi.org/10.1039/b408600gopenalex-snapshot
Anti-inflammatory metabolites from marine sponges
inferredcites →https://doi.org/10.1071/c96120openalex-snapshot
Avarol and Related Compounds from the New Zealand Marine Sponge Dysidea sp.
inferredcites →https://doi.org/10.1093/rheumatology/keh103openalex-snapshot
Osteoarthritis therapy--are there still unmet needs?
inferredcites →https://doi.org/10.1146/annurev.med.53.082901.103952openalex-snapshot
Cyclooxygenase-2: A Therapeutic Target
inferredcites →https://doi.org/10.1517/13543784.13.3.255openalex-snapshot
New therapies for chronic obstructive pulmonary disease
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4780.3.5zenodo-depositor-declared
Description of two new species of Dysidea (Porifera, Demospongiae, Dictyoceratida, Dysideidae) from Tauranga Harbour, Bay of Plenty, New Zealand
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod194openalex-snapshot
Porifera (Sponges)–4
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod195openalex-snapshot
Porifera (Sponges)–5
inferred← citeshttps://doi.org/10.1002/cbdv.201800078openalex-snapshot
Popolohuanones G – I, Dimeric Sesquiterpene Quinones with IL‐6 Inhibitory Activity from the Marine Sponge Dactylospongia elegans
inferred← citeshttps://doi.org/10.1002/hlca.200800349openalex-snapshot
Neobacillamide A, a Novel Thiazole‐Containing Alkaloid from the Marine Bacterium Bacillus vallismortis C89, Associated with South China Sea Sponge Dysidea avara
inferred← citeshttps://doi.org/10.1002/ptr.2063openalex-snapshot
In Vitro acetylcholinesterase inhibitory properties of thymol, carvacrol and their derivatives thymoquinone and thymohydroquinone
inferred← citeshttps://doi.org/10.1007/978-3-030-30402-7_25openalex-snapshot
Bioactive Metabolites from Marine Ascidians: Future Treatment for Autism Spectrum Disorder
inferred← citeshttps://doi.org/10.1007/s10126-003-0007-7openalex-snapshot
Marine Pharmacology in 2000: Marine Compounds with Antibacterial, Anticoagulant, Antifungal, Anti-inflammatory, Antimalarial, Antiplatelet, Antituberculosis, and Antiviral Activities; Affecting the Cardiovascular, Immune, and Nervous Systems and Other Miscellaneous Mechanisms of Action
inferred← citeshttps://doi.org/10.1007/s11356-020-10938-2openalex-snapshot
Exploration of acute toxicity, analgesic, anti-inflammatory, and anti-pyretic activities of the black tunicate, Phallusia nigra (Savigny, 1816) using mice model
inferred← citeshttps://doi.org/10.1007/s11418-017-1130-5openalex-snapshot
Three new sesquiterpene aminoquinones from a Vietnamese Spongia sp. and their biological activities
inferred← citeshttps://doi.org/10.1007/s11426-012-4826-0openalex-snapshot
A nature-inspired concise synthesis of (+)-ent-chromazonarol
inferred← citeshttps://doi.org/10.1016/b978-0-444-53836-9.00023-2openalex-snapshot
Bioactive Marine Prenylated Quinones/Quinols
inferred← citeshttps://doi.org/10.1016/b978-0-444-63473-3.00006-xopenalex-snapshot
Drimane-Related Merosesquiterpenoids, a Promising Library of Metabolites for Drug Development
inferred← citeshttps://doi.org/10.1016/b978-1-78242-086-6.00009-1openalex-snapshot
Anti-inflammatory drug delivery systems using marine products
inferred← citeshttps://doi.org/10.1016/j.algal.2019.101472openalex-snapshot
Prospective natural anti-inflammatory drimanes attenuating pro-inflammatory 5-lipoxygenase from marine macroalga Gracilaria salicornia
inferred← citeshttps://doi.org/10.1016/j.bbagen.2009.03.011openalex-snapshot
Marine pharmacology in 2005–6: Marine compounds with anthelmintic, antibacterial, anticoagulant, antifungal, anti-inflammatory, antimalarial, antiprotozoal, antituberculosis, and antiviral activities; affecting the cardiovascular, immune and nervous systems, and other miscellaneous mechanisms of…
inferred← citeshttps://doi.org/10.1016/j.biopha.2018.02.034openalex-snapshot
Two sesquiterpene aminoquinones protect against oxidative injury in HaCaT keratinocytes via activation of AMPKα/ERK-Nrf2/ARE/HO-1 signaling
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2015.12.008openalex-snapshot
New marine natural products from sponges (Porifera) of the order Dictyoceratida (2001 to 2012); a promising source for drug discovery, exploration and future prospects
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.05.060openalex-snapshot
New merosesquiterpenes from a Vietnamese marine sponge of Spongia sp. and their biological activities
inferred← citeshttps://doi.org/10.1016/j.btre.2016.06.001openalex-snapshot
Antimicrobial activities of secondary metabolites and phylogenetic study of sponge endosymbiotic bacteria, Bacillus sp. at Agatti Island, Lakshadweep Archipelago
inferred← citeshttps://doi.org/10.1016/j.cjnm.2025.100012openalex-snapshot
Ircinrimanes A−J: ten undescribed rearranged 4,9-friedodrimane merosesquiterpenoids with cytotoxic and anti-inflammatory activities from the marine sponge Ircinia sp
inferred← citeshttps://doi.org/10.1016/j.ejca.2004.09.005openalex-snapshot
Marine pharmacology in 2001–2: antitumour and cytotoxic compounds
inferred← citeshttps://doi.org/10.1016/j.ejca.2008.07.001openalex-snapshot
Marine pharmacology in 2005–2006: Antitumour and cytotoxic compounds
inferred← citeshttps://doi.org/10.1016/j.phytol.2016.08.012openalex-snapshot
New antibacterial sesquiterpene aminoquinones from a Vietnamese marine sponge of Spongia sp.
inferred← citeshttps://doi.org/10.1016/j.procbio.2011.02.003openalex-snapshot
Bacillamide C production by the optimized cultivation of the Bacillus atrophaeus strain C89 associated with the South China Sea sponge Dysidea avara
inferred← citeshttps://doi.org/10.1016/j.tet.2008.04.012openalex-snapshot
Orthidines A–E, tubastrine, 3,4-dimethoxyphenethyl-β-guanidine, and 1,14-sperminedihomovanillamide: potential anti-inflammatory alkaloids isolated from the New Zealand ascidian Aplidium orthium that act as inhibitors of neutrophil respiratory burst
inferred← citeshttps://doi.org/10.1016/j.tet.2008.04.091openalex-snapshot
Stereochemical evaluation of sesquiterpene quinones from two sponges of the genus Dactylospongia and the implication for enantioselective processes in marine terpene biosynthesis
inferred← citeshttps://doi.org/10.1016/j.tet.2016.05.073openalex-snapshot
Total synthesis of dysidavarone A
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/10.1021/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.5b01067openalex-snapshot
Cystoseira usneoides: A Brown Alga Rich in Antioxidant and Anti-inflammatory Meroditerpenoids
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00471openalex-snapshot
Cinerols, Nitrogenous Meroterpenoids from the Marine Sponge Dysidea cinerea
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.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/np060188lopenalex-snapshot
E/Z-Rubrolide O, an Anti-inflammatory Halogenated Furanone from the New Zealand Ascidian Synoicum n. sp.
inferred← citeshttps://doi.org/10.1021/np060626oopenalex-snapshot
Anti-inflammatory Thiazine Alkaloids Isolated from the New Zealand AscidianAplidiumsp.: Inhibitors of the Neutrophil Respiratory Burst in a Model of Gouty Arthritis
inferred← citeshttps://doi.org/10.1021/np070436topenalex-snapshot
An Antiproliferative Bis-prenylated Quinone from the New Zealand Brown Alga Perithalia capillaris
inferred← citeshttps://doi.org/10.1021/np4009392openalex-snapshot
Dysideanones A–C, Unusual Sesquiterpene Quinones from the South China Sea Sponge Dysidea avara
inferred← citeshttps://doi.org/10.1021/ol202994copenalex-snapshot
Dysidavarones A–D, New Sesquiterpene Quinones from the Marine Sponge Dysidea avara
inferred← citeshttps://doi.org/10.1038/ja.2010.134openalex-snapshot
Two novel alkaloids from the South China Sea marine sponge Dysidea sp.
inferred← citeshttps://doi.org/10.1039/c2ob06825gopenalex-snapshot
Colour-responsive fluorescent oxy radical sensors
inferred← citeshttps://doi.org/10.1039/c3ra47265eopenalex-snapshot
Dysidaminones A–M, cytotoxic and NF-κB inhibitory sesquiterpene aminoquinones from the South China Sea sponge Dysidea fragilis
inferred← citeshttps://doi.org/10.1039/c5ra18876hopenalex-snapshot
Bioactive sesquiterpene quinols and quinones from the marine sponge Dysidea avara
inferred← citeshttps://doi.org/10.1039/c8ob01580eopenalex-snapshot
Unusual anti-inflammatory meroterpenoids from the marine sponge Dactylospongia sp.
inferred← citeshttps://doi.org/10.1039/d4np00025kopenalex-snapshot
Siccanin-related drimane meroterpenoids: biological activities and synthesis
inferred← citeshttps://doi.org/10.1080/14786419.2019.1633644openalex-snapshot
Cytotoxic meroterpenoids from the marine sponge Dactylospongia elegans
inferred← citeshttps://doi.org/10.1080/24750573.2019.1673945openalex-snapshot
Thymoquinone (TQ) demonstrates its neuroprotective effect via an anti-inflammatory action on the A β (1–42) -infused rat model of Alzheimer's disease
inferred← citeshttps://doi.org/10.1186/s43094-023-00550-9openalex-snapshot
The marine sponge genus Dysidea sp: the biological and chemical aspects—a review
inferred← citeshttps://doi.org/10.1248/cpb.c16-00183openalex-snapshot
Antibacterial Meroterpenoids from the South China Sea Sponge Dysidea sp.
inferred← citeshttps://doi.org/10.1371/journal.pone.0114761openalex-snapshot
Anti-Inflammatory Effects of Secondary Metabolites of Marine Pseudomonas sp. in Human Neutrophils Are through Inhibiting P38 MAPK, JNK, and Calcium Pathways
inferred← citeshttps://doi.org/10.2174/138161212802083644openalex-snapshot
Molecules of Natural Origin, Semi-synthesis and Synthesis with Anti-Inflammatory and Anticancer Utilities
inferred← citeshttps://doi.org/10.2174/157019310791384128openalex-snapshot
Quinone/Hydroquinone Sesquiterpenes
inferred← citeshttps://doi.org/10.2174/2210315505666150827212323openalex-snapshot
Novel Anti-inflammatory Drugs from Marine Microbes
inferred← citeshttps://doi.org/10.3389/fmars.2019.00632openalex-snapshot
Application of in situ Solid-Phase Microextraction on Mediterranean Sponges for Untargeted Exometabolome Screening and Environmental Monitoring
inferred← citeshttps://doi.org/10.3390/md11051602openalex-snapshot
Meroterpenes from Marine Invertebrates: Structures, Occurrence, and Ecological Implications
inferred← citeshttps://doi.org/10.3390/md20020118openalex-snapshot
Xishaeleganins A–D, Sesquiterpenoid Hydroquinones from Xisha Marine Sponge Dactylospongia elegans
inferred← citeshttps://doi.org/10.3390/molecules191118025openalex-snapshot
Dysidinoid A, an Unusual Meroterpenoid with Anti-MRSA Activity from the South China Sea Sponge Dysidea sp.
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