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Sesquiterpenes from the Sponge Axinyssa isabela
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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/chin.200417290openalex-snapshot
Marine Isocyanides and Related Natural Products — Structure, Biosynthesis and Ecology
inferredcites →https://doi.org/10.1002/hlca.200790044openalex-snapshot
Aristolane Sesquiterpenes and Highly Brominated Indoles from the Marine Red Alga Laurencia similis (Rhodomelaceae)
inferredcites →https://doi.org/10.1002/hlca.200790059openalex-snapshot
New Nitrogenous Bisabolene‐Type Sesquiterpenes from a Hainan Sponge Axinyssa aff. variabilis
inferredcites →https://doi.org/10.1007/978-3-7091-6331-3openalex-snapshot
Progress in the Chemistry of Organic Natural Products
inferredcites →https://doi.org/10.1016/0040-4020(95)01079-3openalex-snapshot
Terpenoids with antifouling activity against barnacle larvae from the marine sponge Acanthella cavernosa
inferredcites →https://doi.org/10.1016/j.bmc.2004.03.067openalex-snapshot
Antitumor agents. Part 227: Studies on novel 4′-O-demethyl-epipodophyllotoxins as antitumor agents targeting topoisomerase II
inferredcites →https://doi.org/10.1016/j.bmcl.2006.11.070openalex-snapshot
Synthesis and anti-HIV-1 activities of novel podophyllotoxin derivatives
inferredcites →https://doi.org/10.1016/j.tet.2006.08.070openalex-snapshot
Stereochemical challenges in characterizing nitrogenous spiro-axane sesquiterpenes from the Indo-Pacific sponges Amorphinopsis and Axinyssa
inferredcites →https://doi.org/10.1016/j.tet.2007.08.028openalex-snapshot
New diastereomeric bis-sesquiterpenes from Hainan marine sponges Axinyssa variabilis and Lipastrotethya ana
inferredcites →https://doi.org/10.1016/s0031-9422(00)83460-3openalex-snapshot
Oxidized aristolane sesquiterpenes from Aristolochia debilis
inferredcites →https://doi.org/10.1016/s0040-4020(01)81280-1openalex-snapshot
Acanthenes A to C: a chloro, isothiocyanate, formamide sesquiterpene triad isolated from the Northeastern Pacific marine sponge Acanthella sp. and the dorid nudibranch Cadlina luteomarginata
inferredcites →https://doi.org/10.1016/s0040-4020(98)00867-9openalex-snapshot
Five new antifouling sesquiterpenes from two marine sponges of the genus Axinyssa and the nudibranch Phyllidia pustulosa
inferredcites →https://doi.org/10.1016/s0040-4039(00)93525-1openalex-snapshot
Cyanopuupehenol, an antiviral metabolite of a sponge of the order Verongida
inferredcites →https://doi.org/10.1016/s0040-4039(98)01251-9openalex-snapshot
New nardosinane and aristolane sesquiterpenes from the fruiting bodies of Russula lepida
inferredcites →https://doi.org/10.1016/s0040-4039(99)01559-2openalex-snapshot
Sandresolides A and B: novel nor-diterpenes from the sea whip Pseudopterogorgia elisabethae (Bayer)
inferredcites →https://doi.org/10.1016/s0957-4166(01)00508-0openalex-snapshot
A practical guide for the assignment of the absolute configuration of alcohols, amines and carboxylic acids by NMR
inferredcites →https://doi.org/10.1021/cr000665jopenalex-snapshot
The Assignment of Absolute Configuration by NMR
inferredcites →https://doi.org/10.1021/jo00076a012openalex-snapshot
Biogenetically diverse, bioactive constituents of a sponge, order Verongida: bromotyramines and sesquiterpene-shikimate derived metabolites
inferredcites →https://doi.org/10.1021/jo00171a057openalex-snapshot
An aristolane sesquiterpenoid from the sea pen Scytalium splendens
inferredcites →https://doi.org/10.1021/jo00282a043openalex-snapshot
5-Isothiocyanatopupukeanane from a sponge of the genus Axinyssa
inferredcites →https://doi.org/10.1021/jo00376a015openalex-snapshot
Nitrogenous bisabolene sesquiterpenes from marine invertebrates
inferredcites →https://doi.org/10.1021/np030237jopenalex-snapshot
New 9-Thiocyanatopupukeanane Sesquiterpenes from the Nudibranch Phyllidia v aricosa and Its Sponge-Prey Axinyssa a culeata
inferredcites →https://doi.org/10.1021/np030349aopenalex-snapshot
New Nitrogenous Germacranes from a Thai Marine Sponge, Axinyssa n. sp.
inferredcites →https://doi.org/10.1021/np0400961openalex-snapshot
Isocyanide Terpene Metabolites of Phyllidiella pustulosa, a Nudibranch from the South China Sea
inferredcites →https://doi.org/10.1021/np049798gopenalex-snapshot
Boneratamides A−C, New Sesquiterpenoids Isolated from the Marine Sponge Axinyssa a plysinoides
inferredcites →https://doi.org/10.1021/np070593sopenalex-snapshot
Isothiocyanate Sesquiterpenes from a Sponge of the GenusAxinyssa
inferredcites →https://doi.org/10.1021/np50083a012openalex-snapshot
Two New Sesquiterpene Isothiocyanates from the Marine Sponge Acanthella klethra
inferredcites →https://doi.org/10.1021/np50094a009openalex-snapshot
Sesquiterpenoids and Norsesquiterpenoids from the Soft Coral Lemnalia africana
inferredcites →https://doi.org/10.1021/np50096a016openalex-snapshot
Bioactive and Other Sesquiterpenoids from Porella cordeana
inferredcites →https://doi.org/10.1021/np50115a024openalex-snapshot
Metabolites of the Palauan Sponge Axinyssa aplysinoides
inferredcites →https://doi.org/10.1021/ol027202fopenalex-snapshot
(−)-Axinyssene: A Novel Cytotoxic Diterpene from a Japanese Marine Sponge Axinyssa sp
inferredcites →https://doi.org/10.1039/b302359copenalex-snapshot
Marine isocyanides and related natural products ? structure, biosynthesis and ecology
inferredcites →https://doi.org/10.1071/ch9800681openalex-snapshot
Studies of Australian soft corals. XVI. Two new sesquiterpenes from Lemnalia humesi
inferredcites →https://doi.org/10.1093/jnci/82.13.1107openalex-snapshot
New Colorimetric Cytotoxicity Assay for Anticancer-Drug Screening
inferredcites →https://doi.org/10.11646/zootaxa.1784.1.4openalex-snapshot
First record of Axinyssa Lendenfeld, 1897 (Demospongiae, Halichondrida) from the East Pacific Ocean, with the description of Axinyssa isabela sp. nov.
inferredcites →https://doi.org/10.1246/bcsj.78.1345openalex-snapshot
Isolation of Two 13-epi-Neoverrucosane-Type Diterpenoids from a Marine Sponge Axinyssa tethyoides
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.2021.112927zenodo-depositor-declared
Bisabolane-type sesquiterpenoids: Structural diversity and biological activity
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod192openalex-snapshot
Porifera (Sponges)–2
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod195openalex-snapshot
Porifera (Sponges)–5
inferred← citeshttps://doi.org/10.1002/ajoc.202200007openalex-snapshot
Me3SiCl‐Catalyzed Electrophilic Thiocyanation/Cyclization of Alkynylbenzoates to Synthesize 4‐Thiocyanatoisocourmarins
inferred← citeshttps://doi.org/10.1002/cbdv.202503741openalex-snapshot
Targeting Staphylococcus aureus Biofilms Through Aurisin Derivatives From Neonothopanus nambi of African Origin
inferred← citeshttps://doi.org/10.1002/chem.202004974openalex-snapshot
Design and Use of Electrophilic Thiocyanating and Selenocyanating Reagents: An Interesting Trend for the Construction of SCN‐ and SeCN‐Containing Compounds
inferred← citeshttps://doi.org/10.1002/ejoc.202101255openalex-snapshot
N‐Thiocyanato‐2,10‐camphorsultam Derivatives: Design and Applications of Original Electrophilic Thiocyanating Reagents
inferred← citeshttps://doi.org/10.1007/s00253-018-9560-xopenalex-snapshot
Hydroperoxides derived from marine sources: origin and biological activities
inferred← citeshttps://doi.org/10.1007/s13659-019-0200-7openalex-snapshot
Aristolane-type Sesquiterpenoids from Nardostachys chinensis and Revised Structure of Aristolanhydride
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00845-4openalex-snapshot
8.29 Spectroscopic Analysis: Diastereomeric Derivatization for Spectroscopy
inferred← citeshttps://doi.org/10.1016/b978-0-32-390644-9.00010-xopenalex-snapshot
Spectroscopic Analysis: Diastereomeric Derivatization for Spectroscopy
inferred← citeshttps://doi.org/10.1016/j.cclet.2023.109447openalex-snapshot
Controlled semi‐Pinacol rearrangement on a strained ring: Efficient access to multi‐substituted cyclopropanes by group migration strategy
inferred← citeshttps://doi.org/10.1016/j.fitote.2021.105093openalex-snapshot
Chlorinated bisabolene sesquiterpenoids from the whole plant of Parasenecio rubescens
inferred← citeshttps://doi.org/10.1016/j.phytochem.2012.07.024openalex-snapshot
Terpenoids from Russula lepida and R. amarissima (Basidiomycota, Russulaceae)
inferred← citeshttps://doi.org/10.1016/j.phytol.2013.04.006openalex-snapshot
Novel spiro-sesquiterpene from the mushroom Anthracophyllum sp. BCC18695
inferred← citeshttps://doi.org/10.1016/j.synbio.2026.01.010openalex-snapshot
Targeted identification of new phaterpenes and elucidation of the relevant biosynthetic pathway in Streptomyces phaeochromogenes OSK-123
inferred← citeshttps://doi.org/10.1016/j.tet.2010.07.029openalex-snapshot
An efficient one-pot four-step domino reaction for the synthesis of C2-substituted 3-methylcyclohex-2-enones
inferred← citeshttps://doi.org/10.1016/j.tet.2011.08.050openalex-snapshot
Cationic cyclization of keto-epoxides mediated by zirconium(IV) tetrachloride: diastereoselective synthesis of cis-decalinols
inferred← citeshttps://doi.org/10.1016/j.tet.2012.07.057openalex-snapshot
Cytotoxic sesquiterpenes from luminescent mushroom Neonothopanus nambi
inferred← citeshttps://doi.org/10.1021/acs.chemrev.1c00143openalex-snapshot
Medicinal Chemistry of Isocyanides
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00502openalex-snapshot
Tricyclic Sesquiterpenes from Marine Origin
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00960openalex-snapshot
Hamigerans R and S: Nitrogenous Diterpenoids from the New Zealand Marine Sponge Hamigera tarangaensis
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02530openalex-snapshot
Electrophotocatalytic Thiocyanation and Sulfonylation Cyclization of Unactivated Alkenes
inferred← citeshttps://doi.org/10.1021/jo2001116openalex-snapshot
Cationic Cyclization of 2-Alkenyl-1,3-dithiolanes: Diastereoselective Synthesis of trans-Decalins
inferred← citeshttps://doi.org/10.1038/s41598-017-15483-6openalex-snapshot
Novel serotonin transporter regulators: Natural aristolane- and nardosinane- types of sesquiterpenoids from Nardostachys chinensis Batal
inferred← citeshttps://doi.org/10.1039/c4np00109eopenalex-snapshot
Syntheses and biological studies of marine terpenoids derived from inorganic cyanide
inferred← citeshttps://doi.org/10.1039/c5np00024fopenalex-snapshot
Biological activity of natural sesquiterpenoids containing a gem-dimethylcyclopropane unit
inferred← citeshttps://doi.org/10.1039/d3np00028aopenalex-snapshot
Nitrile biosynthesis in nature: how and why?
inferred← citeshttps://doi.org/10.1039/d4cc03391dopenalex-snapshot
Metal-free radical selenothiocyanation of terminal and internal alkynes
inferred← citeshttps://doi.org/10.1080/14786419.2019.1578763openalex-snapshot
New p-terphenyl and benzoquinone metabolites from the bioluminescent mushroom Neonothopanus nambi
inferred← citeshttps://doi.org/10.1177/1934578x221099973openalex-snapshot
Natural Products Containing the Nitrile Functional Group and Their Biological Activities
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.c15-00051openalex-snapshot
Sesquiterpenes from the Fruiting Bodies of Ramaria formosa and Their Human Neutrophil Elastase Inhibitory Activity
inferred← citeshttps://doi.org/10.12692/ijb/14.3.30-34openalex-snapshot
The brine shrimp toxicity of the philippine marine sponges Axinyssa sp., Plocamionida sp., Forcepia sp., Pachymatisma sp., and Placospongia sp.
inferred← citeshttps://doi.org/10.3390/biomedicines11102698openalex-snapshot
Steroids Bearing Heteroatom as Potential Drugs for Medicine
inferred← citeshttps://doi.org/10.3390/md14010016openalex-snapshot
Marine Isonitriles and Their Related Compounds
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.53897/li.2018.0014.ucolopenalex-snapshot
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