On the public citation graph

Bioactive Diterpenoids from the Stems of Euphorbia antiquorum

0 signed · 84 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cbdv.201300154openalex-snapshot
Daphnane‐Type Diterpenoid Glucosides and Further Constituents of Euphorbia pilosa
inferredcites →https://doi.org/10.1002/cmdc.201500007openalex-snapshot
Development of Urea and Thiourea Kynurenamine Derivatives: Synthesis, Molecular Modeling, and Biological Evaluation as Nitric Oxide Synthase Inhibitors
inferredcites →https://doi.org/10.1002/hlca.200390043openalex-snapshot
Chemical Transformations of Phyllocladane (=13β‐Kaurane) Diterpenoids
inferredcites →https://doi.org/10.1007/s10787-007-0013-xopenalex-snapshot
Role of nitric oxide in inflammatory diseases
inferredcites →https://doi.org/10.1007/s12264-011-1530-6openalex-snapshot
Nitric oxide in neurodegeneration: potential benefits of non-steroidal anti-inflammatories
inferredcites →https://doi.org/10.1007/s12272-015-0648-xopenalex-snapshot
Involvement of inflammation in Alzheimer’s disease pathogenesis and therapeutic potential of anti-inflammatory agents
inferredcites →https://doi.org/10.1016/j.bioorg.2017.09.007openalex-snapshot
Nitric oxide inhibitory daphnane diterpenoids as potential anti-neuroinflammatory agents for AD from the twigs of Trigonostemon thyrsoideus
inferredcites →https://doi.org/10.1016/j.bioorg.2018.02.007openalex-snapshot
Diterpenoids from the roots of Euphorbia ebracteolata and their anti-tuberculosis effects
inferredcites →https://doi.org/10.1016/j.bmcl.2016.05.035openalex-snapshot
Jatrophane and ingenane-type diterpenoids from Euphorbia kansui inhibit the LPS-induced NO production in RAW 264.7 cells
inferredcites →https://doi.org/10.1016/j.fitote.2017.12.006openalex-snapshot
Four new compounds from the roots of Euphorbia ebracteolata and their inhibitory effect on LPS-induced NO production
inferredcites →https://doi.org/10.1016/j.jep.2015.10.025openalex-snapshot
Global medicinal uses of Euphorbia L. (Euphorbiaceae)
inferredcites →https://doi.org/10.1016/j.phytochem.2017.10.006openalex-snapshot
Diterpenes from the stem bark of Euphorbia neriifolia and their in vitro anti-HIV activity
inferredcites →https://doi.org/10.1016/j.phytochem.2017.10.012openalex-snapshot
Highly oxygenated and structurally diverse diterpenoids from Euphorbia helioscopia
inferredcites →https://doi.org/10.1016/j.phytochem.2017.12.005openalex-snapshot
Diterpenoids from the roots of Euphorbia ebracteolata and their inhibitory effects on human carboxylesterase 2
inferredcites →https://doi.org/10.1016/j.phytochem.2018.01.016openalex-snapshot
Jatrophane diterpenoids with multidrug-resistance modulating activity from the latex of Euphorbia nicaeensis
inferredcites →https://doi.org/10.1016/j.phytochem.2018.02.001openalex-snapshot
Seco-labdane diterpenoids from the leaves of Callicarpa nudiflora showing nitric oxide inhibitory activity
inferredcites →https://doi.org/10.1016/s0040-4020(01)86461-9openalex-snapshot
HIV inhibitory natural products. 3. Diterpenes from and
inferredcites →https://doi.org/10.1016/s0165-0173(00)00018-7openalex-snapshot
Roles of NMDA receptor activity and nitric oxide production in brain development
inferredcites →https://doi.org/10.1016/s0367-326x(99)00011-8openalex-snapshot
Ingol diterpene ester from the latex of Euphorbia lactea
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00583openalex-snapshot
Characterization and Biological Evaluation of Diterpenoids from Casearia graveolens
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00789openalex-snapshot
Diterpenoids from the Roots of Euphorbia fischeriana with Inhibitory Effects on Nitric Oxide Production
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00205openalex-snapshot
Euphorbesulins A–P, Structurally Diverse Diterpenoids from Euphorbia esula
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00206openalex-snapshot
Pepluane and Paraliane Diterpenoids from Euphorbia peplus with Potential Anti-inflammatory Activity
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00260openalex-snapshot
Myrsinane, Premyrsinane, and Cyclomyrsinane Diterpenes from Euphorbia falcata as Potassium Ion Channel Inhibitors with Selective G Protein-Activated Inwardly Rectifying Ion Channel (GIRK) Blocking Effects
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00603openalex-snapshot
Isolation of Phorbol Esters fromEuphorbia grandicornisand Evaluation of Protein Kinase C- and Human Platelet-Activating Effects of Euphorbiaceae Diterpenes
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00627openalex-snapshot
Drug Affinity Responsive Target Stability (DARTS) Identifies Laurifolioside as a New Clathrin Heavy Chain Modulator
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00644openalex-snapshot
Euphorbia dendroides Latex as a Source of Jatrophane Esters: Isolation, Structural Analysis, Conformational Study, and Anti-CHIKV Activity
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00733openalex-snapshot
Bioactive Terpenoids from Salvia plebeia: Structures, NO Inhibitory Activities, and Interactions with iNOS
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00786openalex-snapshot
ent-Abietane and Tigliane Diterpenoids from the Roots of Euphorbia fischeriana and Their Inhibitory Effects against Mycobacterium smegmatis
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00990openalex-snapshot
Evaluation of Jatrophane Esters from Euphorbia spp. as Modulators of Candida albicans Multidrug Transporters
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b01084openalex-snapshot
Exploring Jolkinol D Derivatives To Overcome Multidrug Resistance in Cancer
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b01099openalex-snapshot
Terpenoids from Euphorbia soongarica and Their Multidrug Resistance Reversal Activity
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00113openalex-snapshot
Environmentally Friendly Procedure Based on Supercritical Fluid Chromatography and Tandem Mass Spectrometry Molecular Networking for the Discovery of Potent Antiviral Compounds from Euphorbia semiperfoliata
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00233openalex-snapshot
Isolation of Premyrsinane, Myrsinane, and Tigliane Diterpenoids from Euphorbia pithyusa Using a Chikungunya Virus Cell-Based Assay and Analogue Annotation by Molecular Networking
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00332openalex-snapshot
Gaditanone, a Diterpenoid Based on an Unprecedented Carbon Skeleton Isolated from Euphorbia gaditana
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00595openalex-snapshot
Heterodimeric Diterpenoids Isolated fromEuphorbia ebracteolataRoots and Their Inhibitory Effects on α-Glucosidase
inferredcites →https://doi.org/10.1021/acs.joc.7b02558openalex-snapshot
Secoheliosphanes A and B and Secoheliospholane A, Three Diterpenoids with Unusual seco-Jatrophane and seco-Jatropholane Skeletons from Euphorbia helioscopia
inferredcites →https://doi.org/10.1021/acs.joc.7b02684openalex-snapshot
Quorumolides A–C, Three Cembranoids from Euphorbia antiquorum
inferredcites →https://doi.org/10.1021/acs.orglett.6b01093openalex-snapshot
Euphorikanin A, a Diterpenoid Lactone with a Fused 5/6/7/3 Ring System from Euphorbia kansui
inferredcites →https://doi.org/10.1021/acs.orglett.6b03142openalex-snapshot
Euphomilones A and B, ent-Rosane Diterpenoids with 7/5/6 and 5/7/6 Skeletons from Euphorbia milii
inferredcites →https://doi.org/10.1021/acs.orglett.7b01813openalex-snapshot
Natural and Semisynthetic Tigliane Diterpenoids with New Carbon Skeletons from Euphorbia dracunculoides as a Wnt Signaling Pathway Inhibitor
inferredcites →https://doi.org/10.1021/cr078350sopenalex-snapshot
Chemical and Pharmacological Research of the Plants in Genus Euphorbia
inferredcites →https://doi.org/10.1021/cr400541jopenalex-snapshot
Euphorbia Diterpenes: Isolation, Structure, Biological Activity, and Synthesis (2008–2012)
inferredcites →https://doi.org/10.1021/np200317popenalex-snapshot
Identification and Characterization of GABAA Receptor Modulatory Diterpenes from Biota orientalis That Decrease Locomotor Activity in Mice
inferredcites →https://doi.org/10.1021/np4009893openalex-snapshot
5,10-seco-neo-Clerodanes and neo-Clerodanes from Salvia microphylla
inferredcites →https://doi.org/10.1021/np5004752openalex-snapshot
Eurifoloids A–R, Structurally Diverse Diterpenoids from Euphorbia neriifolia
inferredcites →https://doi.org/10.1021/np800816nopenalex-snapshot
Ingol and Ingenol Diterpenes from the Aerial Parts of Euphorbia royleana and Their Antiangiogenic Activities
inferredcites →https://doi.org/10.1038/jcbfm.1994.25openalex-snapshot
Nitric Oxide Synthase Inhibition and Cerebrovascular Regulation
inferredcites →https://doi.org/10.1038/nchembio.115openalex-snapshot
Anchored plasticity opens doors for selective inhibitor design in nitric oxide synthase
inferredcites →https://doi.org/10.1146/annurev.bi.63.070194.001135openalex-snapshot
NITRIC OXIDE: A Physiologic Messenger Molecule
inferredcites →https://doi.org/10.2174/138527210792927717openalex-snapshot
Determination of Absolute Configuration of Natural Products: Theoretical Calculation of Electronic Circular Dichroism as a Tool

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.2021.112846zenodo-depositor-declared
Diterpenoids from the genus Euphorbia: Structure and biological activity (2013–2019)
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113106zenodo-depositor-declared
Diverse diterpenoids with α-glucosidase and β-glucuronidase inhibitory activities from Euphorbia milii
inferred← citeshttps://doi.org/10.1002/cbdv.71521openalex-snapshot
A Bioactive Fraction of Euphorbia antiquorum Stem Powder Ameliorates High‐Fat High‐Fructose Diet/Streptozotocin‐Induced Diabetes via GLUT‐4 Modulation
inferred← citeshttps://doi.org/10.1007/s00299-026-03799-5openalex-snapshot
Salicylic acid-mediated biosynthesis of anti-oomycete diterpenoids in Euphorbia lathyris L. suspension cells
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103741openalex-snapshot
Diterpenoids from the leaves of Casearia kurzii showing cytotoxic activities
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103966openalex-snapshot
Diterpenoids as potential anti-inflammatory agents from Ajuga pantantha
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.105817openalex-snapshot
Natural terpenoids with anti-inflammatory activities: Potential leads for anti-inflammatory drug discovery
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106067openalex-snapshot
Diterpenoids from the whole plant of Euphorbia wallichii and their protective effects on H2O2-induced BV-2 microglial cells injury
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108207openalex-snapshot
20-Deoxyingenol ester and ether derivatives: Synthesis, properties and cytotoxicity
inferred← citeshttps://doi.org/10.1016/j.bse.2023.104739openalex-snapshot
Chemical constituents from Mallotus tetracoccus (Roxb.) Kurz (Euphorbiaceae) and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106350openalex-snapshot
Ingenane diterpenoids with anti-inflammatory activity from Euphorbia antiquorum
inferred← citeshttps://doi.org/10.1016/j.jep.2022.115574openalex-snapshot
Phytochemical and pharmacological review of diterpenoids from the genus Euphorbia Linn (2012–2021)
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112523openalex-snapshot
Diterpenoids from the aerial parts of Euphorbia antiquorum and their efficacy on nitric oxide inhibition
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113502openalex-snapshot
Secotrijugins A−D, four highly oxidized and rearranged limonoids from Trichilia sinensis and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113745openalex-snapshot
Diterpenoids from Euphorbia lactea and their anti-HIV-1 activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113867openalex-snapshot
Cycloartane-type triterpenoids and steroids from Trichilia connaroides and their multidrug resistance reversal activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114657openalex-snapshot
Euphebranes A−G: higher diterpenoids from the radix of Euphorbia ebracteolata
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114947openalex-snapshot
Terpenoids in Euphorbia milii Ch. des Moulins and their anti-rheumatic potential
inferred← citeshttps://doi.org/10.1021/acs.est.9b07324openalex-snapshot
Novel Pathway for Chloramphenicol Catabolism in the Activated Sludge Bacterial Isolate Sphingobium sp. CAP‑1
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00249openalex-snapshot
Euphnerins A and B, Diterpenoids with a 5/6/6 Rearranged Spirocyclic Carbon Skeleton from the Stems of Euphorbia neriifolia
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00629openalex-snapshot
Anti-inflammatory neo -Clerodane Diterpenoids from Ajuga pantantha
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b01281openalex-snapshot
Anti-Inflammatoryent-Kaurane Diterpenoids fromIsodon serra
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00974openalex-snapshot
Evolutionary Efforts in the Total Synthesis of Pepluacetal
inferred← citeshttps://doi.org/10.1021/jacs.6c01271openalex-snapshot
Divergent Syntheses of the Euphorbia Diterpenoids Pepluanol A and Pepluacetal
inferred← citeshttps://doi.org/10.1038/s41467-025-61188-0openalex-snapshot
Divergent multifunctional P450s-empowered biosynthesis of bioactive tripterifordin and cryptic atiserenoids in Aconitum implies convergent evolution
inferred← citeshttps://doi.org/10.1039/d0np00039fopenalex-snapshot
ent -Atisane diterpenoids: isolation, structure and bioactivity
inferred← citeshttps://doi.org/10.1039/d2np00047dopenalex-snapshot
Euphorbia diterpenoids: isolation, structure, bioactivity, biosynthesis, and synthesis (2013–2021)
inferred← citeshttps://doi.org/10.1039/d3ob01007dopenalex-snapshot
Discovery of two ent -atisane diterpenoid lactones with AChE inhibitory activity from the roots of Euphorbia fischeriana
inferred← citeshttps://doi.org/10.1080/14786419.2020.1789634openalex-snapshot
New diterpenoids from the stems of Euphorbia antiquorum growing in Vietnam
inferred← citeshttps://doi.org/10.3390/md23060238openalex-snapshot
New Bioactive Polyketides from the Mangrove-Derived Fungus Daldinia eschscholzii HJX1P2
inferred← citeshttps://doi.org/10.3390/metabo15030177openalex-snapshot
Untargeted Metabolomics and Targeted Phytohormone Profiling of Sweet Aloes (Euphorbia neriifolia) from Guyana: An Assessment of Asthma Therapy Potential in Leaf Extracts and Latex
inferred← citeshttps://doi.org/10.3390/molecules26082257openalex-snapshot
Alpha-Glucosidase Inhibitory Diterpenes from Euphorbia antiquorum Growing in Vietnam
inferred← citeshttps://doi.org/10.3390/plants15111614openalex-snapshot
Heterologous Expression and In Vivo Functional Analysis of OsTPS2 in Yeast, Tobacco, and Rice
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.