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ent-Abietane and Tigliane Diterpenoids from the Roots of Euphorbia fischeriana and Their Inhibitory Effects against Mycobacterium smegmatis

https://doi.org/10.1021/acs.jnatprod.6b00786

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What this work says

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

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cclib: A library for package‐independent computational chemistry algorithms

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Inhibitory effects of Lang-du extract on the in vitro and in vivo growth of melanoma cells and its molecular mechanisms of action

inferredcites →https://doi.org/10.1016/j.carbpol.2011.09.007openalex-snapshot

Chemical structure of one low molecular weight and water-soluble polysaccharide (EFP-W1) from the roots of Euphorbia fischeriana

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A water-soluble polysaccharide (EFP-AW1) from the alkaline extract of the roots of a traditional Chinese medicine, Euphorbia fischeriana: Fraction and characterization

inferredcites →https://doi.org/10.1016/j.chroma.2011.12.017openalex-snapshot

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inferredcites →https://doi.org/10.1016/j.ijbiomac.2011.05.029openalex-snapshot

The extraction process optimization and physicochemical properties of polysaccharides from the roots of Euphorbia fischeriana

inferredcites →https://doi.org/10.1016/j.intimp.2011.10.020openalex-snapshot

17-Hydroxy-jolkinolide B, a diterpenoid from Euphorbia fischeriana, inhibits inflammatory mediators but activates heme oxygenase-1 expression in lipopolysaccharide-stimulated murine macrophages

inferredcites →https://doi.org/10.1016/s0031-9422(00)90670-8openalex-snapshot

A highly oxygenated phenanthrofuran skeleton diterpene from Euphorbia acaulis

inferredcites →https://doi.org/10.1016/s0031-9422(96)00605-xopenalex-snapshot

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Diterpenes and aromatic compounds from Euphorbia fischeriana

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The π-π circular dichroism of δβ-unsaturated γ-lactones

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Langduin C, a novel dimeric diterpenoid from the roots of Euphorbia fischeriana

inferredcites →https://doi.org/10.1016/s0040-4039(98)02455-1openalex-snapshot

Fischeria A, a novel norditerpene lactone from Euphorbia fischeriana

inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00789openalex-snapshot

Diterpenoids from the Roots of Euphorbia fischeriana with Inhibitory Effects on Nitric Oxide Production

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Cytotoxic Sterol Derivatives from a Marine Sponge Homaxinella sp.

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Diterpenoids from the Roots of Euphorbia fischeriana

inferredcites →https://doi.org/10.1021/np200058copenalex-snapshot

Tigliane-Type Diterpenoid Glycosides from Euphorbia fischeriana

inferredcites →https://doi.org/10.1021/np50078a003openalex-snapshot

Structure Elucidation of Helioscopinolides D and E from Euphorbia calyptrata Cell Cultures

inferredcites →https://doi.org/10.1039/c6ay00656fopenalex-snapshot

Microwave-assisted extraction and ionic liquid-based dispersive liquid–liquid microextraction followed by HPLC for the determination of trace components in a Langdu preparation

inferredcites →https://doi.org/10.1055/s-2005-864102openalex-snapshot

Cytotoxic Diterpenoids from the Roots ofEuphorbia ebracteolata

inferredcites →https://doi.org/10.1055/s-2007-969515openalex-snapshot

Isolation of Prostratin fromEuphorbia cornigera

inferredcites →https://doi.org/10.1128/jcm.36.2.362-366.1998openalex-snapshot

Rapid, Low-Technology MIC Determination with Clinical Mycobacterium tuberculosis Isolates by Using the Microplate Alamar Blue Assay

inferredcites →https://doi.org/10.3724/sp.j.1009.2012.00299openalex-snapshot

Chemical constituents of Euphorbia fischeriana

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.2021.112867zenodo-depositor-declared

Euphorfinoids E-L: Diterpenoids from the roots of Euphorbia fischeriana with acetylcholinesterase inhibitory activity

inferred← citeshttps://doi.org/10.1002/cbdv.202000919openalex-snapshot

Cytotoxic Diterpenoids from Euphorbia fischeriana

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

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Naturally Occurring [4+2] Type Terpenoid Dimers Assembled through Unmatched‐electron‐demand Cycloaddition

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inferred← citeshttps://doi.org/10.1007/978-3-031-67180-7_1openalex-snapshot

Tigliane Diterpenoids

inferred← citeshttps://doi.org/10.1007/s10600-023-04091-8openalex-snapshot

A New Diterpenoid with Cytotoxic Activities from the Roots of Euphorbia fischeriana

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Three new ent-abietane diterpenoids from the roots of Euphorbia fischeriana and their cytotoxicity in human tumor cell lines

inferred← citeshttps://doi.org/10.1016/b978-0-443-18611-0.00011-5openalex-snapshot

Natural resource of anti–human immunodeficiency virus leading compounds

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NO inhibitory diterpenoids as potential anti-inflammatory agents from Euphorbia antiquorum

inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105356openalex-snapshot

Bisfischoids A and B, dimeric ent-abietane-type diterpenoids with anti-inflammatory potential from Euphorbia fischeriana Steud.

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Tigliane and rhamnofolane glycosides from Euphorbia wallichii prevent oxidative stress-induced neuronal death in PC-12 cells

inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108851openalex-snapshot

Anti-Mycobacterium tuberculosis activity of 17-hydroxy-jolkinolide B by interacting with RNA polymerase

inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108961openalex-snapshot

Tigliane glycosides from Euphorbia tirucalli as multidrug resistance modulators

inferred← citeshttps://doi.org/10.1016/j.bmc.2025.118294openalex-snapshot

Jolkinolide B inhibits mycobacterial growth by down-regulating ribosomal proteins and interfering with protein synthesis

inferred← citeshttps://doi.org/10.1016/j.cclet.2022.03.003openalex-snapshot

Octacyclic and decacyclic ent‑abietane dimers with cytotoxic activity from Euphorbia fischeriana steud.

inferred← citeshttps://doi.org/10.1016/j.cclet.2024.109955openalex-snapshot

Highly anticipated natural diterpenoids as an important source of new drugs in 2013–2023

inferred← citeshttps://doi.org/10.1016/j.engmic.2022.100058openalex-snapshot

Sustainable biosynthesis of valuable diterpenes in microbes

inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105195openalex-snapshot

An unusual indole-diterpenoid with C-17 norcassane skeleton from Euphorbia fischeriana induces HEL cell cycle arrest and apoptosis

inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107177openalex-snapshot

Tigliane and daphnane diterpenoid glucosides from the roots of Euphorbia fischeriana: isolation, structural elucidation, and anti-inflammatory activity

inferred← citeshttps://doi.org/10.1016/j.jep.2021.114095openalex-snapshot

Existing knowledge on Euphorbia fischeriana Steud. (Euphorbiaceae): Traditional uses, clinical applications, phytochemistry, pharmacology and toxicology

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.micpath.2019.04.002openalex-snapshot

Characterization of serine acetyltransferase (CysE) from methicillin-resistant Staphylococcus aureus and inhibitory effect of two natural products on CysE

inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.112064openalex-snapshot

Euphonoids A−G, cytotoxic diterpenoids from Euphorbia fischeriana

inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112360openalex-snapshot

Anti-HIV tigliane diterpenoids from Reutealis trisperma

inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112437openalex-snapshot

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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.2022.113372openalex-snapshot

Euphorfiatnoids A−I: Diterpenoids from the roots of Euphorbia fischeriana with cytotoxic effects

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113382openalex-snapshot

Diterpene glycosides, acetophenone glycosides and tannins from polar extracts of the root of Euphorbia fischeriana with cytotoxicity and antibacterial activities

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113448openalex-snapshot

Jolkinolide B: A comprehensive review of its physicochemical properties, analytical methods, synthesis and pharmacological activity

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113468openalex-snapshot

Targeted isolation of diterpenoids and sesquiterpenoids from Daphne gemmata E. Pritz. ex Diels using molecular networking together with network annotation propagation and MS2LDA

inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113725openalex-snapshot

Daphnane-type diterpenoids from Stellera chamaejasme L. and their inhibitory activity against hepatocellular carcinoma cells

inferred← citeshttps://doi.org/10.1016/j.phytol.2021.12.002openalex-snapshot

Triterpenoids from Euphorbia fischeriana

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.tube.2017.11.005openalex-snapshot

Quercetin 3-O-glucoside recovered from the wild Egyptian Sahara plant, Euphorbia paralias L., inhibits glutamine synthetase and has antimycobacterial activity

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00147openalex-snapshot

Modified ent-Abietane Diterpenoids from the Leaves of Suregada zanzibariensis

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.jnatprod.9b00134openalex-snapshot

Bioactive Diterpenoids from the Stems of Euphorbia antiquorum

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01114openalex-snapshot

Pepluanols C–D, Two Diterpenoids with Two Skeletons from Euphorbia peplus

inferred← citeshttps://doi.org/10.1039/c7ra11982hopenalex-snapshot

Ent -abietane diterpenoids and their probable biogenetic precursors from the roots of Euphorbia fischeriana

inferred← citeshttps://doi.org/10.1039/c8np00079dopenalex-snapshot

Diterpenoids of terrestrial origin

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Fischernolides A–D, four novel diterpene-based meroterpenoid scaffolds with antitumor activities from Euphorbia fischeriana

inferred← citeshttps://doi.org/10.1039/c9ob00013eopenalex-snapshot

Fischeriana A, a meroterpenoid with an unusual 6/6/5/5/5/6/6 heptacyclic carbon skeleton from the roots of Euphorbia fischeriana

inferred← citeshttps://doi.org/10.1039/d2np00047dopenalex-snapshot

Euphorbia diterpenoids: isolation, structure, bioactivity, biosynthesis, and synthesis (2013–2021)

inferred← citeshttps://doi.org/10.1039/d2ob00053aopenalex-snapshot

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inferred← citeshttps://doi.org/10.1039/d3ob01007dopenalex-snapshot

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inferred← citeshttps://doi.org/10.1039/d4np00021hopenalex-snapshot

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inferred← citeshttps://doi.org/10.1080/10286020.2020.1758931openalex-snapshot

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inferred← citeshttps://doi.org/10.1080/14786419.2018.1470628openalex-snapshot

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inferred← citeshttps://doi.org/10.1080/14786419.2019.1607331openalex-snapshot

A new highly oxygenated abietane diterpenoid and a new lysosome generating phorbol ester from the roots of Euphorbia fischeriana Steud

inferred← citeshttps://doi.org/10.1080/14786419.2019.1616728openalex-snapshot

Bioactive tigliane diterpenoids from the latex of Euphorbia fischeriana

inferred← citeshttps://doi.org/10.1080/14786419.2023.2169686openalex-snapshot

Antiproliferative ent -abietane diterpenoids from Euphorbia fischeriana

inferred← citeshttps://doi.org/10.1097/md.0000000000028348openalex-snapshot

Gastrointestinal discomfort and hypotension in a patient with Reutealis trisperma seeds intoxication

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Integrated Strategy of UHPLC-Q-TOF-MS and Molecular Networking for Identification of Diterpenoids from Euphorbia fischeriana Steud. and Prediction of the Anti-Breast-Cancer Mechanism by the Network Pharmacological Method

inferred← citeshttps://doi.org/10.21577/0100-4042.20170932openalex-snapshot

DITERPENOS ENT-ABIETANOS DE Euphorbia phosphorea (EUPHORBIACEAE)

inferred← citeshttps://doi.org/10.2174/0115680266276938240108060247openalex-snapshot

Tackling Nontuberculous Mycobacteria by Repurposable Drugs and Potential Leads from Natural Products

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First insights into herbivore–plant interaction of the spurge hawkmoth and Euphorbia cyparissias

inferred← citeshttps://doi.org/10.3389/fmicb.2019.01799openalex-snapshot

Action of Dicumarol on Glucosamine-1-Phosphate Acetyltransferase of GlmU and Mycobacterium tuberculosis

inferred← citeshttps://doi.org/10.3389/fphar.2020.00397openalex-snapshot

Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes

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inferred← citeshttps://doi.org/10.3389/fpls.2022.905275openalex-snapshot

Comparative Transcriptomics and Metabolites Analysis of Two Closely Related Euphorbia Species Reveal Environmental Adaptation Mechanism and Active Ingredients Difference

inferred← citeshttps://doi.org/10.3390/molecules23040935openalex-snapshot

Structural Diversity and Biological Activities of Diterpenoids Derived from Euphorbia fischeriana Steud

inferred← citeshttps://doi.org/10.3390/molecules28093873openalex-snapshot

Antibacterial and Antifungal Terpenes from the Medicinal Angiosperms of Asia and the Pacific: Haystacks and Gold Needles

inferred← citeshttps://doi.org/10.3390/molecules28135172openalex-snapshot

Phytochemical Analysis, Antioxidant Activities In Vitro and In Vivo, and Theoretical Calculation of Different Extracts of Euphorbia fischeriana

inferred← citeshttps://doi.org/10.3987/com-20-14223openalex-snapshot

Absolute Configuration of the Butenolide of Abietane

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