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Natural Nitrogenous Sesquiterpenoids and Their Bioactivity: A Review
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ejoc.201100347openalex-snapshot
Dotofide, a Guanidine‐Interrupted Terpenoid from the Marine Slug Doto pinnatifida (Gastropoda, Nudibranchia)
inferredcites →https://doi.org/10.1002/ejoc.201200599openalex-snapshot
N–N‐Coupled Indolo‐sesquiterpene Atropo‐Diastereomers from a Marine‐Derived Actinomycete
inferredcites →https://doi.org/10.1002/hlca.201200066openalex-snapshot
Two New Sesquiterpenes from Euonymus alatus
inferredcites →https://doi.org/10.1007/s11418-018-1232-8openalex-snapshot
Macrolide sesquiterpene pyridine alkaloids from the stems of Tripterygium regelii
inferredcites →https://doi.org/10.1007/s12272-010-2227-5openalex-snapshot
Cytotoxic germacranolide sesquiterpenes from the bark of Magnolia kobus
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.bmcl.2015.12.022openalex-snapshot
A dimeric urea of the bisabolene sesquiterpene from the Okinawan marine sponge Axinyssa sp. inhibits protein tyrosine phosphatase 1B activity in Huh-7 human hepatoma cells
inferredcites →https://doi.org/10.1016/j.drudis.2010.06.002openalex-snapshot
What made sesquiterpene lactones reach cancer clinical trials?
inferredcites →https://doi.org/10.1016/j.fitote.2014.04.014openalex-snapshot
Bioactive sesquiterpene polyol esters from the leaves of Tripterygium wilfordii
inferredcites →https://doi.org/10.1016/j.fitote.2015.06.003openalex-snapshot
Anti-inflammatory sesquiterpene pyridine alkaloids from Tripterygium wilfordii
inferredcites →https://doi.org/10.1016/j.fitote.2016.01.003openalex-snapshot
Volvalerine A, an unprecedented N-containing sesquiterpenoid dimer derivative from Valeriana officinalis var. latifolia
inferredcites →https://doi.org/10.1016/j.fitote.2016.04.016openalex-snapshot
Dihydro-β-agarofuran sesquiterpene polyesters isolated from the stems of Tripterygium regelii
inferredcites →https://doi.org/10.1016/j.fitote.2017.10.003openalex-snapshot
New sesquiterpenoid isonitriles from three species of phyllidid nudibranchs
inferredcites →https://doi.org/10.1016/j.fitote.2019.03.008openalex-snapshot
Commipholactam A, a cytotoxic sesquiterpenoidal lactam from Resina Commiphora
inferredcites →https://doi.org/10.1016/j.fitote.2019.104185openalex-snapshot
Dihydroagarofuran sesquiterpenoids esterified with organic acids from the leaves of Tripterygium wilfordii
inferredcites →https://doi.org/10.1016/j.fitote.2020.104501openalex-snapshot
Dihydro-β-agarofuran sesquiterpenoid derivatives with neuroprotective activity from the leaves of Tripterygium wilfordii
inferredcites →https://doi.org/10.1016/j.phytochem.2011.04.014openalex-snapshot
Antiviral isoindolone derivatives from an endophytic fungus Emericella sp. associated with Aegiceras corniculatum
inferredcites →https://doi.org/10.1016/j.phytol.2012.07.009openalex-snapshot
Three new dihydroagarofuran sesquiterpenoids from Celastrus orbiculatus
inferredcites →https://doi.org/10.1016/j.semcancer.2016.08.006openalex-snapshot
Bioactive natural products in cancer prevention and therapy: Progress and promise
inferredcites →https://doi.org/10.1016/j.tet.2011.05.094openalex-snapshot
Nitrogenous sesquiterpenes from the Thai marine sponge Halichondria sp.
inferredcites →https://doi.org/10.1016/j.tet.2016.05.060openalex-snapshot
Sesquiterpene isocyanides, isothiocyanates, thiocyanates, and formamides from the Thai sponge Halichondria sp.
inferredcites →https://doi.org/10.1016/j.tet.2017.07.027openalex-snapshot
Axiriabilines A-D, uncommon nitrogenous eudesmane-type sesquiterpenes from the Hainan sponge Axinyssa variabilis
inferredcites →https://doi.org/10.1016/j.tetlet.2011.04.105openalex-snapshot
Halichonadins G–J, new sesquiterpenoids from a sponge Halichondria sp.
inferredcites →https://doi.org/10.1016/j.tetlet.2019.03.030openalex-snapshot
Halichonic acid, a new rearranged bisabolene-type sesquiterpene from a marine sponge Halichondria sp.
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00850openalex-snapshot
Aedes aegypti Larvicidal Sesquiterpene Alkaloids from Maytenus oblongata
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b01105openalex-snapshot
Sesquiterpene Quinones/Hydroquinones from the Marine Sponge Spongia pertusa Esper
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00610openalex-snapshot
Lamellodysidines A and B, Sesquiterpenes Isolated from the Marine Sponge Lamellodysidea herbacea
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00615openalex-snapshot
Neuroprotective Dihydroagarofuran Sesquiterpene Derivatives from the Leaves of Tripterygium wilfordii
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00698openalex-snapshot
Nitrobenzoyl Sesquiterpenoids with Cytotoxic Activities from a Marine-Derived Aspergillus ochraceus Fungus
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00921openalex-snapshot
Natural Products Containing a Nitrogen–Sulfur Bond
inferredcites →https://doi.org/10.1021/acs.jnatprod.8b00015openalex-snapshot
Cytotoxic and Antibacterial Eremophilane Sesquiterpenes from the Marine-Derived Fungus Cochliobolus lunatus SCSIO41401
inferredcites →https://doi.org/10.1021/acs.jnatprod.8b00948openalex-snapshot
Isolation of Sesquiterpene–Amino Acid Conjugates, Onopornoids A–D, and a Flavonoid Glucoside from Onopordum alexandrinum
inferredcites →https://doi.org/10.1021/acs.jnatprod.9b00100openalex-snapshot
Clavukoellians A–F, Highly Rearranged Nardosinane Sesquiterpenoids with Antiangiogenic Activity from Clavularia koellikeri
inferredcites →https://doi.org/10.1021/acs.jnatprod.9b00471openalex-snapshot
Cinerols, Nitrogenous Meroterpenoids from the Marine Sponge Dysidea cinerea
inferredcites →https://doi.org/10.1021/acs.jnatprod.9b00648openalex-snapshot
Glechomanamides A–C, Germacrane Sesquiterpenoids with an Unusual Δ8-7,12-Lactam Moiety from Salvia scapiformis and Their Antiangiogenic Activity
inferredcites →https://doi.org/10.1021/acs.jnatprod.9b00886openalex-snapshot
Quintaquinone, a Merosesquiterpene from the Yellow Sponge Verongula cf. rigida Esper
inferredcites →https://doi.org/10.1021/acs.jnatprod.9b01199openalex-snapshot
Polyesterified Sesquiterpenoids from the Seeds of Celastrus paniculatus as Lifespan-Extending Agents for the Nematode Caenorhabditis elegans
inferredcites →https://doi.org/10.1021/acs.jnatprod.9b01285openalex-snapshot
Natural Products as Sources of New Drugs over the Nearly Four Decades from 01/1981 to 09/2019
inferredcites →https://doi.org/10.1021/acs.orglett.8b02511openalex-snapshot
Nardochinoids A–C, Three Dimeric Sesquiterpenoids with Specific Fused-Ring Skeletons from Nardostachys chinensis
inferredcites →https://doi.org/10.1021/acs.orglett.8b03306openalex-snapshot
Vlasoulamine A, a Neuroprotective [3.2.2]Cyclazine Sesquiterpene Lactone Dimer from the Roots of Vladimiria souliei
inferredcites →https://doi.org/10.1021/np1000285openalex-snapshot
Sesquiterpenoid Aminoquinones from the Marine Sponge Dysidea sp.
inferredcites →https://doi.org/10.1021/np100669popenalex-snapshot
Sesquiterpene Benzoxazoles and Sesquiterpene Quinones from the Marine Sponge Dactylospongia elegans
inferredcites →https://doi.org/10.1021/np200014kopenalex-snapshot
Antiplasmodial Sesquiterpene Alkaloids from the Roots of Maytenus mekongensis
inferredcites →https://doi.org/10.1021/np200493topenalex-snapshot
Dihydroagarofuran Derivatives from the Dried Roots of Tripterygium wilfordii
inferredcites →https://doi.org/10.1021/np200906sopenalex-snapshot
Natural Products As Sources of New Drugs over the 30 Years from 1981 to 2010
inferredcites →https://doi.org/10.1021/np300759uopenalex-snapshot
Anti-inflammatory Sesquiterpene Derivatives from the Leaves of Tripterygium wilfordii
inferredcites →https://doi.org/10.1021/np400124nopenalex-snapshot
Natural Products Containing a Nitrogen–Nitrogen Bond
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/np500280xopenalex-snapshot
Nitrogen-Containing Dihydro-β-agarofuran Derivatives from Tripterygium wilfordii
inferredcites →https://doi.org/10.1021/np500317topenalex-snapshot
β-Agarofurans and Sesquiterpene Pyridine Alkaloids from Maytenus spinosa
inferredcites →https://doi.org/10.1021/np500412fopenalex-snapshot
Biotransformation of Huperzine A by a Fungal Endophyte of Huperzia serrata Furnished Sesquiterpenoid–Alkaloid Hybrids
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/np5009569openalex-snapshot
Bisabolane Sesquiterpenoids from the Plant Endophytic Fungus Paraconiothyrium brasiliense
inferredcites →https://doi.org/10.1021/ol301396hopenalex-snapshot
Hybrid Isoprenoids from a Reeds Rhizosphere Soil Derived Actinomycete Streptomyces sp. CHQ-64
inferredcites →https://doi.org/10.1021/ol3014705openalex-snapshot
Halichonadins K and L, New Dimeric Sesquiterpenoids from a Sponge Halichondria sp.
inferredcites →https://doi.org/10.1039/c0np00011fopenalex-snapshot
Xanthane sesquiterpenoids: structure, synthesis and biological activity
inferredcites →https://doi.org/10.1039/c1cc15557aopenalex-snapshot
Halichonines A, B, and C, novel sesquiterpene alkaloids from the marine sponge Halichondria okadai Kadota
inferredcites →https://doi.org/10.1039/c3md00371jopenalex-snapshot
Cytotoxic and antiviral nitrobenzoyl sesquiterpenoids from the marine-derived fungus Aspergillus ochraceus Jcma1F17
inferredcites →https://doi.org/10.1039/c3ra47265eopenalex-snapshot
Dysidaminones A–M, cytotoxic and NF-κB inhibitory sesquiterpene aminoquinones from the South China Sea sponge Dysidea fragilis
inferredcites →https://doi.org/10.1039/c4ra13136copenalex-snapshot
Sesquiterpenoids isolated from an endophyte fungus Diaporthe sp.
inferredcites →https://doi.org/10.1039/c5ob00964bopenalex-snapshot
Natural nitric oxide (NO) inhibitors from the rhizomes of Curcuma phaeocaulis
inferredcites →https://doi.org/10.1039/c6ra01401aopenalex-snapshot
Sporulaminals A and B: a pair of unusual epimeric spiroaminal derivatives from a marine-derived fungus Paraconiothyrium sporulosum YK-03
inferredcites →https://doi.org/10.1039/c8ob01580eopenalex-snapshot
Unusual anti-inflammatory meroterpenoids from the marine sponge Dactylospongia sp.
inferredcites →https://doi.org/10.1039/c9np00062copenalex-snapshot
Natural disesquiterpenoids: an update
inferredcites →https://doi.org/10.1039/c9qo00942fopenalex-snapshot
Nitrogenous cyclonerane sesquiterpenes from an algicolous strain of Trichoderma asperellum
inferredcites →https://doi.org/10.1039/c9qo01248fopenalex-snapshot
Spiroalanpyrroids A and B, sesquiterpene alkaloids with a unique spiro-eudesmanolide–pyrrolizidine skeleton from Inula helenium
inferredcites →https://doi.org/10.1080/10286020.2012.729049openalex-snapshot
Two sesquiterpene pyridine alkaloids and a triterpenoid saponin from the root barks ofTripterygium hypoglaucum
inferredcites →https://doi.org/10.1080/10286020.2012.751098openalex-snapshot
Fasciospyrinadine, a novel sesquiterpene pyridine alkaloid from a Guangxi spongeFasciospongiasp.
inferredcites →https://doi.org/10.1080/10286020.2016.1247810openalex-snapshot
Chemical constituents from the roots of Tripterygium wilfordii and their cytotoxic activity
inferredcites →https://doi.org/10.1080/10286020.2018.1492563openalex-snapshot
Two new sesquiterpene pyridine alkaloids from root barks of Celastrus angulatus
inferredcites →https://doi.org/10.1080/14786419.2012.722086openalex-snapshot
Three bioactive sesquiterpene quinones from the Fijian marine sponge of the genusHippospongia
inferredcites →https://doi.org/10.1080/14786419.2019.1633644openalex-snapshot
Cytotoxic meroterpenoids from the marine sponge Dactylospongia elegans
inferredcites →https://doi.org/10.1080/14786419.2019.1679132openalex-snapshot
Cytotoxic sesquiterpenoid quinones from South China Sea sponge Dysidea sp
inferredcites →https://doi.org/10.1080/14786419.2019.1680669openalex-snapshot
Isolation, structural elucidation, and antimicrobial evaluation of the metabolites from a marine-derived fungus Penicillium sp. ZZ1283
inferredcites →https://doi.org/10.1080/14786419.2020.1712387openalex-snapshot
Phyllanthacidoid U: a new N-glycosyl norbisabolane sesquiterpene from Phyllanthus acidus (L.) skeels
inferredcites →https://doi.org/10.1126/science.1116364openalex-snapshot
The Renaissance of Natural Products as Drug Candidates
inferredcites →https://doi.org/10.1177/1934578x1300800303openalex-snapshot
A New Bioactive Sesquiterpenoid Quinone from the Mediterranean Sea Marine Sponge Dysidea avara
inferredcites →https://doi.org/10.3184/003685017x14876775256129openalex-snapshot
A Hundred Years in the Elucidation of the Structures of Natural Products
inferredcites →https://doi.org/10.3390/ijms140612780openalex-snapshot
Sesquiterpenoids Lactones: Benefits to Plants and People
inferredcites →https://doi.org/10.3390/ijms16059119openalex-snapshot
Further Study on Chemical Constituents of Parnassia wightiana Wall: Four New Dihydro-β-agarofuran Sesquiterpene Polyesters
inferredcites →https://doi.org/10.3390/md13063567openalex-snapshot
Drimane Sesquiterpene-Conjugated Amino Acids from a Marine Isolate of the Fungus Talaromyces minioluteus (Penicillium Minioluteum)
inferredcites →https://doi.org/10.3390/md13095796openalex-snapshot
Nitrogen-Containing Diterpenoids, Sesquiterpenoids, and Nor-Diterpenoids from Cespitularia taeniata
inferredcites →https://doi.org/10.3390/md16040130openalex-snapshot
Antartin, a Cytotoxic Zizaane-Type Sesquiterpenoid from a Streptomyces sp. Isolated from an Antarctic Marine Sediment
inferredcites →https://doi.org/10.3390/md16110438openalex-snapshot
Anti-MRSA Sesquiterpenes from the Semi-Mangrove Plant Myoporum bontioides A. Gray
inferredcites →https://doi.org/10.3390/md17010056openalex-snapshot
Cytotoxic Nitrogenous Terpenoids from Two South China Sea Nudibranchs Phyllidiella pustulosa, Phyllidia coelestis, and Their Sponge-Prey Acanthella cavernosa
inferredcites →https://doi.org/10.3390/md17020098openalex-snapshot
Saccharoquinoline, a Cytotoxic Alkaloidal Meroterpenoid from Marine-Derived Bacterium Saccharomonospora sp.
inferredcites →https://doi.org/10.3390/md17030158openalex-snapshot
A New Sesquiterpenoid Aminoquinone from an Indonesian Marine Sponge
inferredcites →https://doi.org/10.3390/molecules190810898openalex-snapshot
Dereplication Guided Discovery of Secondary Metabolites of Mixed Biosynthetic Origin from Aspergillus aculeatus
inferredcites →https://doi.org/10.3390/molecules21091146openalex-snapshot
Dimacrolide Sesquiterpene Pyridine Alkaloids from the Stems of Tripterygium regelii
inferredcites →https://doi.org/10.3390/molecules24020286openalex-snapshot
Alcyonacea: A Potential Source for Production of Nitrogen-Containing Metabolites
inferredcites →https://doi.org/10.3390/molecules24091817openalex-snapshot
Seven New Drimane-Type Sesquiterpenoids from a Marine-Derived Fungus Paraconiothyrium sporulosum YK-03
inferredcites →https://doi.org/10.3987/com-14-s(k)2openalex-snapshot
Halichonadins M-Q, Sesquiterpenes from an Okinawan Marine Sponge Halichondria sp.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Bisabolane-type sesquiterpenoids: Structural diversity and biological activity
inferred← citeshttps://doi.org/10.1002/cbdv.202100971openalex-snapshot
Endophytic Fungi as a Source of Antiviral Compounds – A Review
inferred← citeshttps://doi.org/10.1007/978-3-032-01098-8_7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.aihch.2022.10.005openalex-snapshot
The literature of heterocyclic chemistry, Part XX, 2020
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104252openalex-snapshot
Cadinane- and drimane-type sesquiterpenoids produced by Paecilomyces sp. TE-540, an endophyte from Nicotiana tabacum L., are acetylcholinesterase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105468openalex-snapshot
Clavipyrrine A, a unique polycyclic nitrogenous meroterpenoid with promising anti-glioma effects isolated from the fungus Clitocybe clavipes
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.105982openalex-snapshot
Cadinane-type sesquiterpenoid dimeric diastereomers hibisceusones A-C from infected stems of Hibiscus tiliaceus with cytotoxic activity against triple-negative breast cancer cells
inferred← citeshttps://doi.org/10.1016/j.fitote.2023.105625openalex-snapshot
Design, synthesis, cytotoxic activity, and in silico studies of nitrogenous stilbenes
inferred← citeshttps://doi.org/10.1016/j.jcou.2020.101325openalex-snapshot
Sustainable synthesis of nitrogen heterocycles from carbon dioxide and aromatic amines over heterogeneous catalysts
inferred← citeshttps://doi.org/10.1016/j.micres.2022.127054openalex-snapshot
Microbiome-based screening and co-fermentation of rhizospheric microorganisms for highly ginsenoside Rg3 production
inferred← citeshttps://doi.org/10.1016/j.pep.2023.106359openalex-snapshot
Identification and characterization of a novel sativene synthase from Fischerella thermalis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114576openalex-snapshot
Eleven undescribed sesquiterpenoids with multiple skeleton types and cytotoxicity from the South China Sea soft coral Lemnalia sp.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114592openalex-snapshot
Norsesquiterpenoids from terrestrial and marine organisms: Chemistry, activity and possible biosynthetic pathways (1963–2024)
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114781openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.phytol.2022.12.008openalex-snapshot
New anti-HBV sesquiterpene glycosides and amino acid–sesquiterpene conjugates from the roots of Saussurea lappa
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.155386openalex-snapshot
The first enantioselective total synthesis of the eremophilane-type sesquiterpenoid (−)-peniroqueforin C
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Nitrogen-Containing Sesquiterpenoids from the Sponge Stellitethya ingens as TRPA1 Antagonists
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02530openalex-snapshot
Electrophotocatalytic Thiocyanation and Sulfonylation Cyclization of Unactivated Alkenes
inferred← citeshttps://doi.org/10.1039/d4ob01589dopenalex-snapshot
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Acidic Ionic Liquids in Ultrasonic Irradiation Conditions Promote the Nucleophilic Addition to Chalcone Derivatives
inferred← citeshttps://doi.org/10.1080/14786419.2021.1888291openalex-snapshot
Alkaloids constituents from the roots of Phragmites australis (Cav.) Trin. ex Steud. with their cytotoxic activities
inferred← citeshttps://doi.org/10.1080/14786419.2025.2586776openalex-snapshot
Two new β -dihydroagarofuran sesquiterpene polyesters from the seeds of Celastrus angulatus Maxim and their nitric oxide inhibitory activity
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Systematic Review of Chemical and Biological Activity Studies of Extracts and Isolated Compounds From Nudibranchs
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1955861/v1openalex-snapshot
Effects of Shading on Photosynthetic Characteristics and Metabolism of Cigar Tobacco Leaves
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Diversity Shifts in the Root Microbiome of Cucumber Under Different Plant Cultivation Substrates
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Integrated characterization of six sesquiterpene synthases unravels diversified terpene biosynthesis in the mint species Leucosceptrum canum
inferred← citeshttps://doi.org/10.3390/biom12081025openalex-snapshot
Structures and Biological Activities of Alkaloids Produced by Mushrooms, a Fungal Subgroup
inferred← citeshttps://doi.org/10.3390/cancers17101625openalex-snapshot
Chemopreventive and Anticancer Activity of Selected Triterpenoids in Melanoma
inferred← citeshttps://doi.org/10.3390/jof11070534openalex-snapshot
Recent Advances in Heterologous Protein Expression and Natural Product Synthesis by Aspergillus
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Bioactive Terpenes from Marine Sponges and Their Associated Organisms
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Bioactive Secondary Metabolites of the Genus Diaporthe and Anamorph Phomopsis from Terrestrial and Marine Habitats and Endophytes: 2010–2019
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In Vitro and In Vivo Toxicity Evaluation of Natural Products with Potential Applications as Biopesticides
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