On the public citation graph

New Bioactive Macrocyclic Diterpenoids from Euphorbia helioscopia

https://doi.org/10.1002/cbdv.201700327
0 signed · 46 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/anie.201000449openalex-snapshot
Glandular Trichomes of Leucosceptrum canum Harbor Defensive Sesterterpenoids
inferredcites →https://doi.org/10.1002/cbdv.201600298openalex-snapshot
Two New Pyripyropenes from the Marine Fungus Fusarium lateritium 2016F18‐1
inferredcites →https://doi.org/10.1002/ejoc.201200733openalex-snapshot
Diterpenes from European Euphorbia Species Serving as Prototypes for Natural‐Product‐Based Drug Discovery
inferredcites →https://doi.org/10.1007/s11250-012-0283-1openalex-snapshot
Anthelmintic and antimicrobial activity of methanolic and aqueous extracts of Euphorbia helioscopia L.
inferredcites →https://doi.org/10.1007/s12272-001-2149-3openalex-snapshot
Cytotoxic macrocyclic diterpenoids from Euphorbia helioscopia
inferredcites →https://doi.org/10.1016/j.aspen.2009.09.002openalex-snapshot
Pesticidal activity of ingenane diterpenes isolated from Euphorbia kansui against Nilaparvata lugens and Tetranychus urticae
inferredcites →https://doi.org/10.1016/j.cclet.2009.09.013openalex-snapshot
A new diterpenoid from Euphorbia helioscopia
inferredcites →https://doi.org/10.1016/j.cclet.2009.10.002openalex-snapshot
A new lathyrane diterpene glycoside from Euphorbia helioscopia L.
inferredcites →https://doi.org/10.1016/j.fitote.2014.03.010openalex-snapshot
Diterpenes inhibiting NO production from Euphorbia helioscopia
inferredcites →https://doi.org/10.1016/j.neulet.2015.12.010openalex-snapshot
15-O-Acetyl-3-O-benzoylcharaciol and helioscopinolide A, two diterpenes isolated from Euphorbia helioscopia suppress microglia activation
inferredcites →https://doi.org/10.1016/j.phytochem.2009.10.005openalex-snapshot
Effects of diterpenes from latex of Euphorbia lactea and Euphorbia laurifolia on human immunodeficiency virus type 1 reactivation
inferredcites →https://doi.org/10.1016/j.phytochem.2015.04.006openalex-snapshot
Ursane-type nortriterpenes with a five-membered A-ring from Rubus innominatus
inferredcites →https://doi.org/10.1016/j.phytochem.2016.12.021openalex-snapshot
Chemical profile and defensive function of the latex of Euphorbia peplus
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/np0706163openalex-snapshot
Cytotoxic Diterpenoids from Euphorbia helioscopia
inferredcites →https://doi.org/10.1055/s-2005-837832openalex-snapshot
Three New Jatrophone-Type Diterpenoids fromEuphorbia helioscopia
inferredcites →https://doi.org/10.1177/1934578x1501001206openalex-snapshot
Macrocyclic Diterpenoids from the Latex of Euphorbia helioscopia
inferredcites →https://doi.org/10.1182/blood.v98.10.3006openalex-snapshot
Prostratin: activation of latent HIV-1 expression suggests a potential inductive adjuvant therapy for HAART
inferredcites →https://doi.org/10.1248/cpb.51.431openalex-snapshot
Three New Ingol Diterpenes from Euphorbia nivulia: Evaluation of Cytotoxic Activity.
inferredcites →https://doi.org/10.1358/dof.2005.030.10.942816openalex-snapshot
PEP-005
inferredcites →https://doi.org/10.3390/molecules16010466openalex-snapshot
Feeding Deterrents against Two Grain Storage Insects from Euphorbia fischeriana
inferredcites →https://doi.org/10.5012/bkcs.2014.35.2.641openalex-snapshot
A New Lathyrane Diterpenoid from the Whole Plant of Euphorbia altotibetica

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.2020.112649zenodo-depositor-declared
Euphorbia helioscopia L.: A phytochemical and pharmacological overview
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/10.22073/pja.v12i2.76943zenodo-depositor-declared
Acaricidal potential of Euphorbia seguieriana and E. helioscopia (Euphorbiaceae) extracts against Tetranychus urticae (Acari: Tetranychidae)
inferred← citeshttps://doi.org/10.1002/cbdv.201800144openalex-snapshot
Lathyrane‐Type Diterpenoids from the Seeds of Euphorbia lathyris L. with Inhibitory Effects on NO Production in RAW 264.7 Cells
inferred← citeshttps://doi.org/10.1002/cbdv.201800386openalex-snapshot
Five New Diterpenoids from the Seeds of Euphorbia lathyris
inferred← citeshttps://doi.org/10.1002/cbdv.202000210openalex-snapshot
Diterpenoids and Flavonoids from the Twigs of Cephalotaxus fortunei var. alpina
inferred← citeshttps://doi.org/10.1002/cbdv.202200918openalex-snapshot
Integration of LC/MS, NMR and Molecular Docking for Profiling of Bioactive Diterpenes from Euphorbia mauritanica L. with in Vitro Anti‐SARS‐CoV‐2 Activity
inferred← citeshttps://doi.org/10.1002/cbdv.202301454openalex-snapshot
ent‐Atisane Diterpenoids from Euphorbia helioscopia and Their Anti‐inflammatory Activities
inferred← citeshttps://doi.org/10.1002/chir.70061openalex-snapshot
Anti‐Inflammatory Jatrophane Diterpenoids With Multiple Chiral Carbon Centers From Jatropha curcas
inferred← citeshttps://doi.org/10.1016/b978-0-12-817905-5.00009-3openalex-snapshot
Jatrophane diterpenes from Euphorbiaceae family
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105139openalex-snapshot
Euphzycopias A−I, macrocyclic diterpenes with NLRP3 inflammasome inhibitory activity from Euphorbia helioscopia L.
inferred← citeshttps://doi.org/10.1016/j.fitote.2023.105614openalex-snapshot
Euphopias G − J, macrocyclic diterpenes with anti-zika virus activity from Euphorbia helioscopia L
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.105821openalex-snapshot
Euphzycopins A − D, macrocyclic diterpenoids with potential anti-inflammatory activity from Euphorbia Helioscopia
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106331openalex-snapshot
Jatrophane diterpenoids from Jatropha curcas with multidrug resistance reversal activity
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.2021.112846openalex-snapshot
Diterpenoids from the genus Euphorbia: Structure and biological activity (2013–2019)
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114233openalex-snapshot
Lathyrane diterpenoids with multidrug resistance reversal activity from the tubers of Euphorbia antiquorum
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00879openalex-snapshot
Jatrophane Diterpenoids with Kv1.3 Ion Channel Inhibitory Effects from Euphorbia helioscopia
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00707openalex-snapshot
Identification of Brassicadiene, a Diterpene Hydrocarbon Attractive to the Invasive Stink Bug Bagrada hilaris, from Volatiles of Cauliflower Seedlings, Brassica oleracea var. botrytis
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c04145openalex-snapshot
Diterpenoids with Rearranged 9(10→11)-abeo-10,12-Cyclojatrophane Skeleton and the First (15S)-Jatrophane from Euphorbia helioscopia: Structural Elucidation, Biomimetic Conversion, and Their Immunosuppressive Effects
inferred← citeshttps://doi.org/10.1039/c8np00079dopenalex-snapshot
Diterpenoids of terrestrial origin
inferred← citeshttps://doi.org/10.1039/d2np00047dopenalex-snapshot
Euphorbia diterpenoids: isolation, structure, bioactivity, biosynthesis, and synthesis (2013–2021)
inferred← citeshttps://doi.org/10.1371/journal.pone.0209870openalex-snapshot
Volatile unsaturated hydrocarbons emitted by seedlings of Brassica species provide host location cues to Bagrada hilaris
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.