On the public citation graph

Identification of New Diterpenoids from Euphorbia calyptrata Cell Cultures

https://doi.org/10.1021/np960127v
0 signed · 56 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1016/0014-4827(68)90403-5openalex-snapshot
Nutrient requirements of suspension cultures of soybean root cells
inferredcites →https://doi.org/10.1021/np50078a003openalex-snapshot
Structure Elucidation of Helioscopinolides D and E from Euphorbia calyptrata Cell Cultures
inferredcites →https://doi.org/10.1055/s-2006-960200openalex-snapshot
Activity on the CNS of Crude Extracts and of Some Diterpenoids Isolated fromEuphorbia calyptrataSuspended Cultures
inferredcites →https://doi.org/10.1107/s0108270183007696openalex-snapshot
Ring asymmetry parameters from out-of-plane atomic displacements

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.2022.113113zenodo-depositor-declared
Pimarane, abietane, and labdane diterpenoids from Euphorbia pekinensis Rupr. and their anti-tumor activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113486zenodo-depositor-declared
Diterpenoids with anti-inflammatory activity from Euphorbia wallichii
inferred← citeshttps://doi.org/10.1002/cbdv.202502359openalex-snapshot
Novel Neuroprotective Phytochemicals From the Roots of Arnebia euchroma : Isolation and Biological Evaluation
inferred← citeshttps://doi.org/10.1002/cjoc.202100367openalex-snapshot
Discovery of Highly Oxidized Abietane Diterpenoids from the Roots of Euphorbia fischeriana with Anti‐tumor Activities
inferred← citeshttps://doi.org/10.1007/978-3-642-56849-7_13openalex-snapshot
The Metabolic Diversity of Plant Cell and Tissue Cultures
inferred← citeshttps://doi.org/10.1007/s10600-018-2510-0openalex-snapshot
Phytochemical Constituents Isolated from Euphorbia rapulum
inferred← citeshttps://doi.org/10.1007/s10600-022-03741-7openalex-snapshot
Chemical Composition of Euphorbia pekinensis
inferred← citeshttps://doi.org/10.1007/s13659-014-0009-3openalex-snapshot
Antifeedant and Antiviral Diterpenoids from the Fresh Roots of Euphorbia jolkinii
inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.07.032openalex-snapshot
Cytotoxic ent-Abietane-type diterpenoids from the roots of Euphorbia ebracteolata
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105442openalex-snapshot
Diterpenoids from Euphorbia glomerulans with potential reversal activities against P-glycoprotein-mediated multidrug resistance
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107989openalex-snapshot
Highly oxygenated ent-abietane diterpenoid lactones from Euphorbia peplus and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.bse.2009.04.003openalex-snapshot
Ent-abietane diterpenoids from Euphorbia guyoniana Boiss. & Reut.
inferred← citeshttps://doi.org/10.1016/j.fitote.2014.06.013openalex-snapshot
Chemical constituents from Euphorbia stracheyi and their biological activities
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.02.026openalex-snapshot
New isopimarane diterpenes and nortriterpene with cytotoxic activity from Ephorbia alatavica Boiss
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106217openalex-snapshot
Bioactive abietenolide diterpenes from Suregada procera
inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107454openalex-snapshot
Euphiquorins A-E, five new structurally diverse diterpenoids from Euphorbia antiquorum L.
inferred← citeshttps://doi.org/10.1016/j.jep.2010.09.003openalex-snapshot
Anti-inflammatory principles of Suregada multiflora against nitric oxide and prostaglandin E2 releases
inferred← citeshttps://doi.org/10.1016/j.phytochem.2006.09.031openalex-snapshot
Potential anti-allergic ent-kaurene diterpenes from the bark of Suregada multiflora
inferred← citeshttps://doi.org/10.1016/j.phytochem.2007.01.017openalex-snapshot
Diterpenoids and triterpenoids from Euphorbia guyoniana
inferred← citeshttps://doi.org/10.1016/j.phytochem.2011.11.016openalex-snapshot
Diterpenoids from Euphorbia neriifolia
inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.10.012openalex-snapshot
Highly oxygenated and structurally diverse diterpenoids from Euphorbia helioscopia
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112593openalex-snapshot
Eupholides A−H, abietane diterpenoids from the roots of Euphorbia fischeriana, and their bioactivities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114653openalex-snapshot
Diterpenoids and sesquiterpenoids from Euphorbia helioscopia and their neuroprotective activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114842openalex-snapshot
Molecular networking-guided discovery of anti-inflammatory diterpenoids from the roots of Euphorbia prolifera
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114934openalex-snapshot
Structurally diverse diterpenoids from Euphorbia milii: Discovery and RORγt-binding evaluation
inferred← citeshttps://doi.org/10.1016/j.phytol.2020.03.002openalex-snapshot
Cytotoxic diterpenoids from the roots of Euphorbia stracheyi
inferred← citeshttps://doi.org/10.1016/j.phytol.2023.02.009openalex-snapshot
Three new abietane diterpenoids from the aerial parts of Euphorbia fischeriana and their cytotoxic effects
inferred← citeshttps://doi.org/10.1016/j.tet.2014.02.082openalex-snapshot
Efficient transformation of 7,14-dihydroxy-ent-kaurenes to novel ent-abietanes having cis-fused α-methylene γ-lactones under Mitsunobu reaction conditions and their cytotoxicities
inferred← citeshttps://doi.org/10.1016/j.tetlet.2003.12.041openalex-snapshot
Efficient synthesis of novel cytotoxic cis-fused α-methylene γ-lactones from 7,14-dihydroxy-ent-kaurenes by transformation under Mitsunobu reaction conditions
inferred← citeshttps://doi.org/10.1016/s0367-326x(99)00134-3openalex-snapshot
Polycyclic diterpenoids from Euphorbia characias
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00041openalex-snapshot
Euphohelides A–C, ent-Abietane-Type Norditerpene Lactones from Euphorbia helioscopia and Their Anti-Inflammatory Activities
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00580openalex-snapshot
Diterpenoids from Euphorbia fischeriana with Kv1.3 Inhibitory Activity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b01099openalex-snapshot
Terpenoids from Euphorbia soongarica and Their Multidrug Resistance Reversal Activity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00326openalex-snapshot
Terpenoids fromEuphorbia pedroias Multidrug-Resistance Reversers
inferred← citeshttps://doi.org/10.1021/np900127jopenalex-snapshot
Diterpenoids and Triterpenoids from Euphorbia retusa
inferred← citeshttps://doi.org/10.1021/np900305jopenalex-snapshot
Chemical Constituents of the Roots of Euphorbia micractina
inferred← citeshttps://doi.org/10.1021/np980333yopenalex-snapshot
Isoterracinolides A and B, Novel Bishomoditerpene Lactones fromEuphorbia terracina
inferred← citeshttps://doi.org/10.1039/a815093yopenalex-snapshot
Diterpenoids
inferred← citeshttps://doi.org/10.1039/c5ra02174jopenalex-snapshot
Bioactive 18(4 → 3)-abeo-abietanoid derivatives from the leaves of Tripterygium wilfordii
inferred← citeshttps://doi.org/10.1080/10286020.2019.1611787openalex-snapshot
Two new ent-abietane diterpenoids from Euphorbia helioscopia
inferred← citeshttps://doi.org/10.1080/14786419.2023.2169686openalex-snapshot
Antiproliferative ent -abietane diterpenoids from Euphorbia fischeriana
inferred← citeshttps://doi.org/10.1080/14786419.2023.2207134openalex-snapshot
Three new diterpenoids isolated from Euphorbia nematocypha Hand.-Mazz and their anti-fungal activity
inferred← citeshttps://doi.org/10.1155/2012/498373openalex-snapshot
Anti-Inflammatory Effects of Concentrated Ethanol Extracts of Edelweiss (Leontopodium alpinumCass.) Callus Cultures towards Human Keratinocytes and Endothelial Cells
inferred← citeshttps://doi.org/10.1246/cl.130280openalex-snapshot
Jolkinolide F, a Cytotoxic Diterpenoid from Euphorbia jolkinii
inferred← citeshttps://doi.org/10.25259/ajc_253_2026openalex-snapshot
Ent-abietane diterpenoid Enantiomers from Euphorbia helioscopia inhibits liver fibrosis via suppressing the TGF-β1/smad pathway
inferred← citeshttps://doi.org/10.3390/molecules14114454openalex-snapshot
13C-NMR Data of Three Important Diterpenes Isolated from Euphorbia Species
inferred← citeshttps://doi.org/10.3390/molecules17022082openalex-snapshot
Regulated Expressions of MMP-2, -9 by Diterpenoids from Euphorbia formosana Hayata
inferred← citeshttps://doi.org/10.3390/molecules27134282openalex-snapshot
Chemical Composition, Anti-Breast Cancer Activity and Extraction Techniques of Ent-Abietane Diterpenoids from Euphorbia fischeriana Steud
inferred← citeshttps://doi.org/10.3390/molecules29174104openalex-snapshot
Diterpenoids with Potent Anti-Psoriasis Activity from Euphorbia helioscopia L.
inferred← citeshttps://doi.org/10.3390/pharmaceutics16081094openalex-snapshot
Anti-Inflammatory, Antibacterial, Anti-Biofilm, and Anti-Quorum Sensing Activities of the Diterpenes Isolated from Clinopodium bolivianum
inferred← citeshttps://doi.org/10.3390/plants12223836openalex-snapshot
Indonesian Euphorbiaceae: Ethnobotanical Survey, In Vitro Antibacterial, Antitumour Screening and Phytochemical Analysis of Euphorbia atoto
inferred← citeshttps://doi.org/10.4028/www.scientific.net/amr.396-398.1337openalex-snapshot
Chemical Constituents from Euphorbia helioscopia
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.