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Four New Diterpenoids from the Roots of Euphorbia pekinensis

https://doi.org/10.1002/cbdv.201600091
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What this work says

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

inferredcites →https://doi.org/10.1002/hlca.200890230openalex-snapshot
Eight New Diterpenoids from the Roots of Euphorbia nematocypha
inferredcites →https://doi.org/10.1016/j.bmc.2009.11.055openalex-snapshot
Isolation, structure, and bioactivities of abiesadines A–Y, 25 new diterpenes from Abies georgei Orr
inferredcites →https://doi.org/10.1016/j.fitote.2009.06.014openalex-snapshot
A new cytotoxic casbane diterpene from Euphorbia pekinensis
inferredcites →https://doi.org/10.1016/j.fitote.2013.07.004openalex-snapshot
A new cytotoxic cembrane diterpene from the roots of Euphorbia pekinensis Rupr
inferredcites →https://doi.org/10.1016/j.fitote.2016.03.008openalex-snapshot
Diterpenoids from the branch and leaf of Abies fargesii
inferredcites →https://doi.org/10.1016/j.phytochem.2013.06.009openalex-snapshot
Casbane diterpenoids from the roots of Euphorbia pekinensis
inferredcites →https://doi.org/10.1016/j.tet.2008.02.069openalex-snapshot
Abiesanordines A–N: fourteen new norditerpenes from Abies georgei
inferredcites →https://doi.org/10.1016/j.tet.2012.11.089openalex-snapshot
Anti-Coxsackie virus B diterpenes from the roots of Illicium jiadifengpi
inferredcites →https://doi.org/10.1016/j.tet.2014.05.006openalex-snapshot
Diterpenes and sesquiterpenes with anti-Coxsackie virus B3 activity from the stems of Illicium jiadifengpi
inferredcites →https://doi.org/10.1016/s0031-9422(00)90652-6openalex-snapshot
Abietanes from leaves of Juniperus chinensis
inferredcites →https://doi.org/10.1016/s0031-9422(03)00154-7openalex-snapshot
Antifungal isopimaranes from Hypoestes serpens
inferredcites →https://doi.org/10.1021/np000595bopenalex-snapshot
Cytotoxic Pheophorbide-Related Compounds from Clerodendrum calamitosum and C. cyrtophyllum
inferredcites →https://doi.org/10.1021/np0202475openalex-snapshot
New Chemical Constituents of Euphorbia q uinquecostata and Absolute Configuration Assignment by a Convenient Mosher Ester Procedure Carried Out in NMR Tubes
inferredcites →https://doi.org/10.1021/np060325eopenalex-snapshot
Fungal Biotransformation Products of Dehydroabietic Acid
inferredcites →https://doi.org/10.1021/np3006925openalex-snapshot
Antidepressant Abietane Diterpenoids from Chinese Eaglewood
inferredcites →https://doi.org/10.1021/np5004752openalex-snapshot
Eurifoloids A–R, Structurally Diverse Diterpenoids from Euphorbia neriifolia
inferredcites →https://doi.org/10.1021/np50078a003openalex-snapshot
Structure Elucidation of Helioscopinolides D and E from Euphorbia calyptrata Cell Cultures
inferredcites →https://doi.org/10.1021/np8002063openalex-snapshot
Abietane Diterpenoids from the Bark of Cryptomeria fortunei
inferredcites →https://doi.org/10.1055/s-2002-23132openalex-snapshot
Cytotoxic Diterpenoids from Euphorbia pekinensis
inferredcites →https://doi.org/10.1080/10286020.2011.596828openalex-snapshot
Two new casbane diterpenoids from the roots ofEuphorbia pekinensis
inferredcites →https://doi.org/10.1080/10286020008041364openalex-snapshot
An Isopimarane Diterpene fromEuphorbia EbracteolataHayata
inferredcites →https://doi.org/10.1080/14786419.2015.1027704openalex-snapshot
A new casbane diterpene fromEuphorbia pekinensis
inferredcites →https://doi.org/10.1093/jnci/82.13.1107openalex-snapshot
New Colorimetric Cytotoxicity Assay for Anticancer-Drug Screening
inferredcites →https://doi.org/10.1590/s0100-40422010000100006openalex-snapshot
Abietatrienes diterpenoids from Sagittaria montevidensis SSP Montevidensis
inferredcites →https://doi.org/10.3109/13880209.2013.818039openalex-snapshot
Cytotoxic and potential anticancer constituents from the stems ofSchisandra pubescens
inferredcites →https://doi.org/10.3390/molecules17089716openalex-snapshot
Diterpenoids from the Buds of Pinus banksiana Lamb.
inferredcites →https://doi.org/10.3724/sp.j.1009.2013.00177openalex-snapshot
Isolation of an anti-complementary polysaccharide from the root of Bupleurum chinense and identification of its targets in complement activation cascade

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.2022.113113zenodo-depositor-declared
Pimarane, abietane, and labdane diterpenoids from Euphorbia pekinensis Rupr. and their anti-tumor activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113154zenodo-depositor-declared
Characterization of undescribed melanoma inhibitors from Euphorbia mauritanica L. cultivated in Egypt targeting BRAFV600E and MEK 1 kinases via in-silico study and ADME prediction
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/10.1007/s11418-024-01816-zopenalex-snapshot
Hinokione: an abietene diterpene with pancreatic β cells regeneration and hypoglycemic activity, and other derivatives with novel structures from the woods of Agathis dammara
inferred← citeshttps://doi.org/10.1016/j.arabjc.2024.106012openalex-snapshot
Cytotoxic diterpenoids from the roots of Euphorbia jolkinii Boiss against human pancreatic cancer SW1990 cells by regulating the expressions of Bcl-2, Bax, and Caspase-3 proteins
inferred← citeshttps://doi.org/10.1016/j.biochi.2017.11.006openalex-snapshot
Upregulation of aquaporin 3 expression by diterpenoids in Euphorbia pekinensis is associated with activation of the NF-κB signaling pathway in the co-culture system of HT-29 and RAW 264.7 cells
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103256openalex-snapshot
Anti-inflammatory evaluation and structure-activity relationships of diterpenoids isolated from Euphorbia hylonoma
inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107119openalex-snapshot
New terpenoids from Euphorbia pekinensis with potent and selective anti-hepatocellular carcinoma 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.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.2023.113784openalex-snapshot
Yuexiandajisu diterpenoids from Euphorbia ebracteolata Hayata (Langdu roots): An overview
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.plgene.2017.07.001openalex-snapshot
De novo transcriptome sequencing and analysis of Euphorbia pekinensis Rupr. and identification of genes involved in diterpenoid biosynthesis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00365openalex-snapshot
Phytotoxic ent-Isopimarane-Type Diterpenoids from Euphorbia hylonoma
inferred← citeshttps://doi.org/10.1039/c6np00059bopenalex-snapshot
Diterpenoids of terrestrial origin
inferred← citeshttps://doi.org/10.1039/c7np00040eopenalex-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/10.1080/14786419.2020.1765342openalex-snapshot
Euphopanes A–C, three new diterpenoids from Euphorbia pekinensis
inferred← citeshttps://doi.org/10.1080/14786419.2024.2397554openalex-snapshot
Euphorbia pekinensis Rupr. roots: a comprehensive review of botany, traditional uses, phytochemistry, pharmacology, quality control, and toxicology
inferred← citeshttps://doi.org/10.3390/molecules22030465openalex-snapshot
Laxative Effects of Total Diterpenoids Extracted from the Roots of Euphorbia pekinensis Are Attributable to Alterations of Aquaporins in the Colon
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