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Ingol-Type Diterpenes from Euphorbia antiquorum with Mouse 11β-Hydroxysteroid Dehydrogenase Type 1 Inhibition Activity

https://doi.org/10.1021/np5002237
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What this work says

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

inferredcites →https://doi.org/10.1016/0031-9422(90)80134-3openalex-snapshot
Constituents of the latex of Euphorbia antiquorum
inferredcites →https://doi.org/10.1016/0031-9422(90)85373-nopenalex-snapshot
Revised structure of a diterpene from Euphorbia antiquorum
inferredcites →https://doi.org/10.1016/0040-4039(84)80128-8openalex-snapshot
Five ingol esters and a 17-hydroxyingenol ester from the latex of . Assignment of esters using 13C.N.M.R. methods.
inferredcites →https://doi.org/10.1016/0957-4166(95)00205-4openalex-snapshot
Preparation of (2R,3S)-(−)- and (2S,3R)-(+)-2,3-epoxy-2-methylbutanoic acids and some of their esters
inferredcites →https://doi.org/10.1016/j.bbagen.2006.05.009openalex-snapshot
Ursolic acid and its derivative inhibit protein tyrosine phosphatase 1B, enhancing insulin receptor phosphorylation and stimulating glucose uptake
inferredcites →https://doi.org/10.1016/j.bmc.2009.05.082openalex-snapshot
Discovery of novel dual functional agent as PPARγ agonist and 11β-HSD1 inhibitor for the treatment of diabetes
inferredcites →https://doi.org/10.1016/j.fitote.2010.10.015openalex-snapshot
Macrocyclic diterpenoids from the Iranian plant Euphorbia bungei Boiss.
inferredcites →https://doi.org/10.1016/j.phytochem.2006.06.030openalex-snapshot
Chemistry and biological activity of secondary metabolites in Euphorbia from Iran
inferredcites →https://doi.org/10.1016/s0031-9422(01)00461-7openalex-snapshot
Macrocyclic diterpenes from Euphorbia nivulia
inferredcites →https://doi.org/10.1016/s0031-9422(97)00018-6openalex-snapshot
Ingenane and lathyrane diterpenes from the latex of Euphorbia canariensis
inferredcites →https://doi.org/10.1016/s0040-4039(01)86984-7openalex-snapshot
Ingol - a new macrocyclic diterpene alcohol from euphorbia ingens
inferredcites →https://doi.org/10.1016/s0957-4166(98)00025-1openalex-snapshot
Enantioselective preparation of (2R,3R)-(+)- and (2S,3S)-(−)-2,3-epoxy-2-methylbutanoic acids and some derivatives
inferredcites →https://doi.org/10.1021/cr078350sopenalex-snapshot
Chemical and Pharmacological Research of the Plants in Genus Euphorbia
inferredcites →https://doi.org/10.1021/np100320hopenalex-snapshot
Trigoxyphins A−G: Diterpenes from Trigonostemon xyphophylloides
inferredcites →https://doi.org/10.1021/np400260gopenalex-snapshot
11β-HSD1 Inhibitors from Walsura cochinchinensis
inferredcites →https://doi.org/10.1021/ol050206aopenalex-snapshot
Lathyranoic Acid A: First Secolathyrane Diterpenoid in Nature fromEuphorbia lathyris
inferredcites →https://doi.org/10.1021/ol901506xopenalex-snapshot
Trigochilides A and B, Two Highly Modified Daphnane-Type Diterpenoids from Trigonostemon chinensis
inferredcites →https://doi.org/10.1089/adt.2005.3.367openalex-snapshot
Development and Application of a Scintillation Proximity Assay (SPA) for Identification of Selective Inhibitors of 11β-Hydroxysteroid Dehydrogenase Type 1
inferredcites →https://doi.org/10.1248/cpb.37.1547openalex-snapshot
Four ingol type diterpenes from Euphorbia antiquorum L.

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/10.1002/9781119152125.ch9openalex-snapshot
Use of Medicinal Plants in Aquaculture
inferred← citeshttps://doi.org/10.1002/cbdv.201700560openalex-snapshot
Terpenes from Euphorbia antiquorum and Their in Vitro Anti‐ HIV Activity
inferred← citeshttps://doi.org/10.1002/cbdv.202400331openalex-snapshot
A Review on Ethnobotany, Phytochemistry and Pharmacological Activities of Euphorbia antiquorum L.
inferred← citeshttps://doi.org/10.1007/s11426-016-0233-1openalex-snapshot
Attractive natural products with strained cyclopropane and/or cyclobutane ring systems
inferred← citeshttps://doi.org/10.1016/j.bioorg.2016.12.004openalex-snapshot
Protein tyrosine phosphatase 1B inhibitors as antidiabetic agents – A brief review
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103237openalex-snapshot
NO inhibitory diterpenoids as potential anti-inflammatory agents from Euphorbia antiquorum
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103292openalex-snapshot
Discovery of diverse diterpenoid scaffolds from Euphorbia antiquorum and their activity against RANKL-induced osteoclastogenesis
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103546openalex-snapshot
Ingol diterpenoids as P-glycoprotein-dependent multidrug resistance (MDR) reversal agents from Euphorbia marginata
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104583openalex-snapshot
Diterpenes with potential treatment of vitiligo from the aerials parts of Euphorbia antiquorum L
inferred← citeshttps://doi.org/10.1016/j.jmgm.2016.10.020openalex-snapshot
Multiple machine learning based descriptive and predictive workflow for the identification of potential PTP1B inhibitors
inferred← citeshttps://doi.org/10.1016/j.nexres.2026.102321openalex-snapshot
Euphorbia royleana Boiss., as a source of bioactive compounds: Traditional uses and pharmacological evidence
inferred← citeshttps://doi.org/10.1016/j.phrs.2022.106158openalex-snapshot
Potential of diterpenes as antidiabetic agents: Evidence from clinical and pre-clinical studies
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112395openalex-snapshot
Diterpenoids from Euphorbia royleana reverse P-glycoprotein-mediated multidrug resistance in cancer cells
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.2022.113344openalex-snapshot
Ingol, ent-atisane, and stachane-type diterpenoids from Euphorbia deightonii with multidrug resistance reversing 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.2024.114233openalex-snapshot
Lathyrane diterpenoids with multidrug resistance reversal activity from the tubers of Euphorbia antiquorum
inferred← citeshttps://doi.org/10.1016/j.phytol.2023.03.011openalex-snapshot
Euphpepluone S, a new lathyrane diterpenoid with anti-inflammatory activity from Euphorbia peplus L.
inferred← citeshttps://doi.org/10.1016/j.tet.2022.132955openalex-snapshot
Phonerilins A–K, cytotoxic ingenane and ingol diterpenoids from Euphorbia neriifolia
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152203openalex-snapshot
Saudiarabicains A-E, bioactive 19-acetoxyingol diterpenoids from Euphorbia saudiarabica
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00205openalex-snapshot
Euphorbesulins A–P, Structurally Diverse Diterpenoids from Euphorbia esula
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00365openalex-snapshot
Phytotoxic ent-Isopimarane-Type Diterpenoids from Euphorbia hylonoma
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02684openalex-snapshot
Quorumolides A–C, Three Cembranoids from Euphorbia antiquorum
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00787openalex-snapshot
Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus
inferred← citeshttps://doi.org/10.1021/np500896nopenalex-snapshot
Hupehenols A–E, Selective 11β-Hydroxysteroid Dehydrogenase Type 1 (11β-HSD1) Inhibitors from Viburnum hupehense
inferred← citeshttps://doi.org/10.1039/c5np00087dopenalex-snapshot
Diterpenoids of terrestrial origin
inferred← citeshttps://doi.org/10.1039/c6np00059bopenalex-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/10.1080/10286020.2018.1498084openalex-snapshot
New ingol-type diterpenes from the latex of Euphorbia resinifera
inferred← citeshttps://doi.org/10.1080/14786419.2019.1629917openalex-snapshot
A new ent-atisane diterpenoid from the aerial parts of Euphorbia antiquorum L.
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/10.1080/14786419.2021.1993215openalex-snapshot
New ingenane and ingol diterpenoids from Euphorbia royleana
inferred← citeshttps://doi.org/10.1080/14786419.2023.2183201openalex-snapshot
A partial peroxisome proliferator-activated receptor gamma agonist isolated from the roots of Euphorbia sikkimensis
inferred← citeshttps://doi.org/10.1080/14786419.2026.2663132openalex-snapshot
Terpenoids from Euphorbia ebracteolata (Hayata.) with their multidrug resistance reversal activity
inferred← citeshttps://doi.org/10.1177/1934578x1501001209openalex-snapshot
Terpenoids and Steroids from Euphorbia hypericifolia
inferred← citeshttps://doi.org/10.1360/ssc-2022-0203openalex-snapshot
The discovery and study of structurally intriguing bioactive natural molecules from medicinal plants: from year 2012 to 2022
inferred← citeshttps://doi.org/10.3390/molecules27072206openalex-snapshot
Antimicrobial Triterpenoids and Ingol Diterpenes from Propolis of Semi-Arid Region of Morocco
inferred← citeshttps://doi.org/10.3390/ph15070780openalex-snapshot
Pharmacological Potential of Lathyrane-Type Diterpenoids from Phytochemical Sources
inferred← citeshttps://doi.org/10.70675/de077b36z969az434fz8320zab7d4caed333openalex-snapshot
Host-parasite interactions of coral reef fish
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