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Activity of Macrocyclic Jatrophane Diterpenes from Euphorbia kansui in a TrkA Fibroblast Survival Assay
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0092-8674(91)90629-dopenalex-snapshot
Trkl3 mediates BDNF/NT-3-dependent survival and proliferation in fibroblasts lacking the low affinity NGF receptor
inferredcites →https://doi.org/10.1016/s0031-9422(99)00088-6openalex-snapshot
Jatrophane diterpenoids from Euphorbia peplus
inferredcites →https://doi.org/10.1016/s0040-4020(00)00982-0openalex-snapshot
Euphosalicin, a new diterpene polyester with multidrug resistance reversing activity from Euphorbia salicifolia
inferredcites →https://doi.org/10.1021/np960669copenalex-snapshot
Macrocyclic Diterpene Polyesters of the Jatrophane Type from Euphorbia esula
inferredcites →https://doi.org/10.1351/pac197541010175openalex-snapshot
Toxic substances of Euphorbiaceae
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.2021.112775zenodo-depositor-declared
Ingenane and jatrophane-type diterpenoids from Euphorbia kansui with multidrug resistance reversal activity
inferred← citeshttps://doi.org/10.1002/ange.201302268openalex-snapshot
Neurotrophe Naturstoffe – ihre Chemie und Biologie
inferred← citeshttps://doi.org/10.1002/anie.201302268openalex-snapshot
Neurotrophic Natural Products: Chemistry and Biology
inferred← citeshttps://doi.org/10.1002/bmc.5282openalex-snapshot
LC–MS/MS method for determination of kansuinine a in rat plasma and its application to a rat pharmacokinetic study
inferred← citeshttps://doi.org/10.1002/ejoc.201200733openalex-snapshot
Diterpenes from European Euphorbia Species Serving as Prototypes for Natural‐Product‐Based Drug Discovery
inferred← citeshttps://doi.org/10.1002/jsfa.7380openalex-snapshot
Ingenane‐type diterpene compounds from Euphorbia kansui modulate IFN ‐γ production through NF‐κB activation
inferred← citeshttps://doi.org/10.1002/jssc.202200792openalex-snapshot
Dissecting chemical markers for controlling “Paozhi” method of traditional Chinese medicine with untargeted metabolomics: Vinegar‐baked Euphorbia kansui as a case study
inferred← citeshttps://doi.org/10.1002/ptr.3640openalex-snapshot
Bioactivity‐guided Isolation of Antiproliferative Diterpenoids from Euphorbia kansui
inferred← citeshttps://doi.org/10.1007/978-3-031-42422-9_1openalex-snapshot
Neurotrophic Natural Products
inferred← citeshttps://doi.org/10.1007/s11101-020-09667-8openalex-snapshot
Jatrophane and rearranged jatrophane-type diterpenes: biogenesis, structure, isolation, biological activity and SARs (1984–2019)
inferred← citeshttps://doi.org/10.1007/s11418-009-0366-0openalex-snapshot
Bioassay-guided separation of the proinflammatory constituents from the roots of Euphorbia kansui
inferred← citeshttps://doi.org/10.1007/s12272-012-0905-1openalex-snapshot
Ingenane-type diterpenes with a modulatory effect on IFN-γ production from the roots of Euphorbia kansui
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.bmcl.2016.05.035openalex-snapshot
Jatrophane and ingenane-type diterpenoids from Euphorbia kansui inhibit the LPS-induced NO production in RAW 264.7 cells
inferred← citeshttps://doi.org/10.1016/j.bmcl.2018.02.050openalex-snapshot
Two new lathyrane-type diterpenoid glycosides with IL-6 production inhibitory activity from the roots of Euphorbia kansui
inferred← citeshttps://doi.org/10.1016/j.ejmech.2007.03.016openalex-snapshot
Anti-tumor 12-deoxyphorbol esters from Euphorbia cornigera
inferred← citeshttps://doi.org/10.1016/j.jep.2020.112557openalex-snapshot
Effect of the vinegar-process on chemical compositions and biological activities of Euphorbia kansui: A review
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112257openalex-snapshot
Ingenane and jatrophane diterpenoids from Euphorbia kansui and their antiproliferative effects
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113449openalex-snapshot
Triterpenoids, steroids and other constituents from Euphorbia kansui and their anti-inflammatory and anti-tumor properties
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114369openalex-snapshot
Jatrophane and ingenane diterpenoids with anti-inflammatory activity from Euphorbia esula
inferred← citeshttps://doi.org/10.1016/j.phytol.2021.03.023openalex-snapshot
New ingenane diterpenoids from Euphorbia kansui reverse multi-drug resistance
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.06.046openalex-snapshot
Concise synthesis of a highly functionalized cyclopentane segment: toward the total synthesis of kansuinine A
inferred← citeshttps://doi.org/10.1016/s1875-5364(13)60021-7openalex-snapshot
Euphorbia kansui roots induced-diarrhea in mice correlates with inflammatory response
inferred← citeshttps://doi.org/10.1016/s2225-4110(16)30066-9openalex-snapshot
Recent Progress of Research on Herbal Products Used in Traditional Chinese Medicine: the Herbs belonging to The Divine Husbandman's Herbal Foundation Canon (神農本草經 Shén Nóng Běn Cǎo Jīng)
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1021/cr078350sopenalex-snapshot
Chemical and Pharmacological Research of the Plants in Genus Euphorbia
inferred← citeshttps://doi.org/10.1021/np0706163openalex-snapshot
Cytotoxic Diterpenoids from Euphorbia helioscopia
inferred← citeshttps://doi.org/10.1021/np800816nopenalex-snapshot
Ingol and Ingenol Diterpenes from the Aerial Parts of Euphorbia royleana and Their Antiangiogenic Activities
inferred← citeshttps://doi.org/10.1039/c0np00017eopenalex-snapshot
Bringing natural products into the fold – exploring the therapeutic lead potential of secondary metabolites for the treatment of protein-misfolding-related neurodegenerative diseases
inferred← citeshttps://doi.org/10.1039/c9cc08830jopenalex-snapshot
Concise gram-scale synthesis of Euphorikanin A skeleton through a domino ring-closing metathesis strategy
inferred← citeshttps://doi.org/10.1055/a-0646-4306openalex-snapshot
Anti-inflammatory Ingenane Diterpenoids from the Roots of Euphorbia kansui
inferred← citeshttps://doi.org/10.1080/14786419.2010.496367openalex-snapshot
Triterpenoids with neurotrophic activity fromGanoderma lucidum
inferred← citeshttps://doi.org/10.1142/s0192415x16500154openalex-snapshot
The Chemical and Biological Properties of Euphorbia kansui
inferred← citeshttps://doi.org/10.1186/s12906-016-1039-7openalex-snapshot
Ultra-performance liquid chromatography-quadrupole/time-of-flight mass spectrometry analysis of the impact of processing on toxic components of Kansui Radix
inferred← citeshttps://doi.org/10.1365/s10337-009-1258-xopenalex-snapshot
LC–DAD–ESI-MS–MS Separation and Chemical Characterization of the Inflammatory Fraction of the Roots of Euphorbia kansui
inferred← citeshttps://doi.org/10.1515/znc-2008-1-210openalex-snapshot
Termiticidal Activity of Diterpenes from the Roots of Euphorbia kansui
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4158295/v1openalex-snapshot
Transcriptome profiling on Euphorbia kansui elicited with methyl jasmonate
inferred← citeshttps://doi.org/10.3390/ijms130911247openalex-snapshot
Bio-Guided Isolation of the Cytotoxic Terpenoids from the Roots of Euphorbia kansui against Human Normal Cell Lines L-O2 and GES-1
inferred← citeshttps://doi.org/10.3390/ijms160818956openalex-snapshot
A Natural Triterpene Derivative from Euphorbia kansui Inhibits Cell Proliferation and Induces Apoptosis against Rat Intestinal Epithelioid Cell Line in Vitro
inferred← citeshttps://doi.org/10.3390/molecules21060813openalex-snapshot
An Ingenol Derived from Euphorbia kansui Induces Hepatocyte Cytotoxicity by Triggering G0/G1 Cell Cycle Arrest and Regulating the Mitochondrial Apoptosis Pathway in Vitro
inferred← citeshttps://doi.org/10.3390/molecules31173024openalex-snapshot
Jatrophane Diterpenoids from Euphorbia peplus with LysoTracker-Associated Cellular Activity
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