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Bioactive Segetane, Ingenane, and Jatrophane Diterpenes from Euphorbia taurinensis

https://doi.org/10.1055/a-0589-0525
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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/ejoc.201200733openalex-snapshot
Diterpenes from European Euphorbia Species Serving as Prototypes for Natural‐Product‐Based Drug Discovery
inferredcites →https://doi.org/10.1002/ptr.3640openalex-snapshot
Bioactivity‐guided Isolation of Antiproliferative Diterpenoids from Euphorbia kansui
inferredcites →https://doi.org/10.1007/978-3-7091-8714-2_1openalex-snapshot
Pro-Inflammatory, Tumour-Promoting and Anti-Tumour Diterpenes of the Plant Families Euphorbiaceae and Thymelaeaceae
inferredcites →https://doi.org/10.1016/j.bcp.2008.11.025openalex-snapshot
SJ23B, a jatrophane diterpene activates classical PKCs and displays strong activity against HIV in vitro
inferredcites →https://doi.org/10.1016/j.bmcl.2016.04.064openalex-snapshot
Identification of selenocompounds with promising properties to reverse cancer multidrug resistance
inferredcites →https://doi.org/10.1016/j.fitote.2015.05.012openalex-snapshot
Cyparissins A and B, jatrophane diterpenes from Euphorbia cyparissias as Pgp inhibitors and cytotoxic agents against ovarian cancer cell lines
inferredcites →https://doi.org/10.1016/j.phymed.2016.05.007openalex-snapshot
Jatrophane diterpenes and cancer multidrug resistance – ABCB1 efflux modulation and selective cell death induction
inferredcites →https://doi.org/10.1016/j.tet.2005.02.031openalex-snapshot
Amygdaloidins A–L, twelve new 13 α-OH jatrophane diterpenes from Euphorbia amygdaloides L.
inferredcites →https://doi.org/10.1016/s0021-9258(18)61633-3openalex-snapshot
Certain calcium channel blockers bind specifically to multidrug-resistant human KB carcinoma membrane vesicles and inhibit drug binding to P-glycoprotein.
inferredcites →https://doi.org/10.1016/s0031-9422(01)00393-4openalex-snapshot
Diterpenoids from Euphorbia paralias
inferredcites →https://doi.org/10.1016/s0031-9422(97)00830-3openalex-snapshot
Diterpenes from Euphorbia segetalis
inferredcites →https://doi.org/10.1016/s0031-9422(97)00832-7openalex-snapshot
Diterpenes from Euphorbia paralias
inferredcites →https://doi.org/10.1016/s0040-4020(97)00032-xopenalex-snapshot
Paralinones A and B, novel diterpene esters from Euphorbia paralias
inferredcites →https://doi.org/10.1021/acs.jmedchem.5b01233openalex-snapshot
Gnidimacrin, a Potent Anti-HIV Diterpene, Can Eliminate Latent HIV-1 Ex Vivo by Activation of Protein Kinase C β
inferredcites →https://doi.org/10.1021/acs.orglett.5b03473openalex-snapshot
One-Step Semisynthesis of a Segetane Diterpenoid from a Jatrophane Precursor via a Diels–Alder Reaction
inferredcites →https://doi.org/10.1021/ci200145popenalex-snapshot
Toward a Better Pharmacophore Description of P-Glycoprotein Modulators, Based on Macrocyclic Diterpenes fromEuphorbiaSpecies
inferredcites →https://doi.org/10.1021/cr400541jopenalex-snapshot
Euphorbia Diterpenes: Isolation, Structure, Biological Activity, and Synthesis (2008–2012)
inferredcites →https://doi.org/10.1021/jm0111301openalex-snapshot
Discovery and Biological Evaluation of a New Family of Potent Modulators of Multidrug Resistance: Reversal of Multidrug Resistance of Mouse Lymphoma Cells by New Natural Jatrophane Diterpenoids Isolated from Euphorbia Species
inferredcites →https://doi.org/10.1021/np060046ropenalex-snapshot
Euphoportlandols A and B, Tetracylic Diterpene Polyesters from Euphorbia p ortlandica and Their Anti-MDR Effects in Cancer Cells
inferredcites →https://doi.org/10.1021/np070174vopenalex-snapshot
Antimalarial and Antituberculous Poly-O-acylated Jatrophane Diterpenoids from Pedilanthus tithymaloides
inferredcites →https://doi.org/10.1021/np500271uopenalex-snapshot
Jatrophane Diterpenes as Inhibitors of Chikungunya Virus Replication: Structure–Activity Relationship and Discovery of a Potent Lead
inferredcites →https://doi.org/10.1021/ol701454vopenalex-snapshot
Biogenetical Related Highly Oxygenated Macrocyclic Diterpenes from Sea Spurge Euphorbia paralias
inferredcites →https://doi.org/10.1074/jbc.m402124200openalex-snapshot
Prostratin Antagonizes HIV Latency by Activating NF-κB
inferredcites →https://doi.org/10.12705/622.3openalex-snapshot
A worldwide molecular phylogeny and classification of the leafy spurges, Euphorbia subgenus Esula (Euphorbiaceae)
inferredcites →https://doi.org/10.1371/journal.pone.0108887openalex-snapshot
Intra-Lesional Injection of the Novel PKC Activator EBC-46 Rapidly Ablates Tumors in Mouse Models
inferredcites →https://doi.org/10.1515/znb-1984-0525openalex-snapshot
On the Active Principles of the Euphorbiaceae, IXa Ingenane Type Diterpene Esters from Five Euphorbia Species
inferredcites →https://doi.org/10.2174/156802611796904924openalex-snapshot
Therapeutic Targeting of TRPV1 by Resiniferatoxin, from Preclinical Studies to Clinical Trials

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/10.1007/s11101-020-09667-8openalex-snapshot
Jatrophane and rearranged jatrophane-type diterpenes: biogenesis, structure, isolation, biological activity and SARs (1984–2019)
inferred← citeshttps://doi.org/10.1016/b978-0-12-817905-5.00009-3openalex-snapshot
Jatrophane diterpenes from Euphorbiaceae family
inferred← citeshttps://doi.org/10.1016/b978-0-12-819541-3.00009-8openalex-snapshot
Potential for cancer treatment: natural products from the Balkans
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107194openalex-snapshot
Diterpenoids from Euphorbia peplus possessing cytotoxic and anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108207openalex-snapshot
20-Deoxyingenol ester and ether derivatives: Synthesis, properties and cytotoxicity
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2020.10.192openalex-snapshot
Aerodynamic properties and in silico deposition of isoniazid loaded chitosan/thiolated chitosan and hyaluronic acid hybrid nanoplex DPIs as a potential TB treatment
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.tet.2022.132955openalex-snapshot
Phonerilins A–K, cytotoxic ingenane and ingol diterpenoids from Euphorbia neriifolia
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00654openalex-snapshot
Macrocyclic Diterpenoid Constituents of Euphorbia deflexa, an Endemic Spurge from Greece
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00500openalex-snapshot
Diterpenoids from Euphorbia dulcis with Potassium Ion Channel Inhibitory Activity with Selective G Protein-Activated Inwardly Rectifying Ion Channel (GIRK) Blocking Effect
inferred← citeshttps://doi.org/10.1039/d2np00047dopenalex-snapshot
Euphorbia diterpenoids: isolation, structure, bioactivity, biosynthesis, and synthesis (2013–2021)
inferred← citeshttps://doi.org/10.14232/phd.11777openalex-snapshot
Isolation and structure elucidation of biological active compounds from Euphorbia deightonii and Centrapalus pauciflorus
inferred← citeshttps://doi.org/10.3389/fphar.2020.00397openalex-snapshot
Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes
inferred← citeshttps://doi.org/10.3389/fphar.2022.815603openalex-snapshot
Research Progress on Natural Diterpenoids in Reversing Multidrug Resistance
inferred← citeshttps://doi.org/10.3390/cancers16010114openalex-snapshot
Nature’s Green Potential: Anticancer Properties of Plants of the Euphorbiaceae Family
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