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Diterpenoids from the Roots of Euphorbia fischeriana

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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/s0040-4039(01)92614-0openalex-snapshot

Crystal and molecular structure of jolkinolide B, a novel oxidolactone diterpene

inferredcites →https://doi.org/10.1016/s0223-5234(01)01302-2openalex-snapshot

Medicinal natural products: A biosynthetic approach

inferredcites →https://doi.org/10.1021/ja9532345openalex-snapshot

Structure Determination of an Endogenous Sleep-Inducing Lipid, cis-9-Octadecenamide (Oleamide): A Synthetic Approach to the Chemical Analysis of Trace Quantities of a Natural Product

inferredcites →https://doi.org/10.1021/jm00089a006openalex-snapshot

A nonpromoting phorbol from the Samoan medicinal plant Homalanthus nutans inhibits cell killing by HIV-1

inferredcites →https://doi.org/10.1021/jm950509iopenalex-snapshot

Selectively Cytotoxic Diterpenes from Euphorbia poisonii

inferredcites →https://doi.org/10.1093/jnci/83.11.757openalex-snapshot

Feasibility of a High-Flux Anticancer Drug Screen Using a Diverse Panel of Cultured Human Tumor Cell Lines

inferredcites →https://doi.org/10.1093/jnci/83.11.766openalex-snapshot

Effects of a Low-Fat Diet on Levels of Oxidative Damage to DNA in Human Peripheral Nucleated Blood Cells

inferredcites →https://doi.org/10.1139/v99-218openalex-snapshot

New abietane diterpenoids from the cones of Larix kaempferi

inferredcites →https://doi.org/10.1182/blood.v98.10.3006openalex-snapshot

Prostratin: activation of latent HIV-1 expression suggests a potential inductive adjuvant therapy for HAART

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.2022.113142zenodo-depositor-declared

Phorneroids A–M, diverse types of diterpenoids from Euphorbia neriifolia

inferred← citeshttps://doi.org/10.1002/bmc.3000openalex-snapshot

LC‐ESI‐MS/MS analysis and pharmacokinetics of jolkinolide B, a potential antitumor active component isolated from Euphorbia fischeriana, in rat plasma

inferred← citeshttps://doi.org/10.1002/cbdv.201000115openalex-snapshot

Chemical Constituents and Biological Activities of Euphorbia fischeriana Steud .

inferred← citeshttps://doi.org/10.1002/cbdv.201300154openalex-snapshot

Daphnane‐Type Diterpenoid Glucosides and Further Constituents of Euphorbia pilosa

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

Cytotoxic Diterpenoids from Euphorbia fischeriana

inferred← citeshttps://doi.org/10.1002/mc.22948openalex-snapshot

Ethyl gallate as a novel ERK1/2 inhibitor suppresses patient‐derived esophageal tumor growth

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

Tigliane Diterpenoids

inferred← citeshttps://doi.org/10.1007/978-3-319-20397-3_3openalex-snapshot

Jatropha Natural Products as Potential Therapeutic Leads

inferred← citeshttps://doi.org/10.1007/s10616-010-9283-zopenalex-snapshot

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

inferred← citeshttps://doi.org/10.1007/s11418-015-0940-6openalex-snapshot

ent-Atisane diterpenoids from Euphorbia fischeriana inhibit mammosphere formation in MCF-7 cells

inferred← citeshttps://doi.org/10.1007/s11904-024-00712-1openalex-snapshot

Medicinal Plant and Traditional Knowledge-guided Strategies to Combat HIV Persistence

inferred← citeshttps://doi.org/10.1007/s12272-019-01151-yopenalex-snapshot

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/b978-0-12-398371-8.00002-7openalex-snapshot

Terpenes

inferred← citeshttps://doi.org/10.1016/b978-0-443-18611-0.00007-3openalex-snapshot

Casbene-derived diterpenoids

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

Natural resource of anti–human immunodeficiency virus leading compounds

inferred← citeshttps://doi.org/10.1016/j.amjms.2024.09.004openalex-snapshot

Study on the mechanism of 17-Hydroxy-jolkinolide B on anaplastic thyroid cancer cell

inferred← citeshttps://doi.org/10.1016/j.aquaculture.2013.09.022openalex-snapshot

The efficacy of four common anthelmintic drugs and traditional Chinese medicinal plant extracts to control Dactylogyrus vastator (Monogenea)

inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.109020openalex-snapshot

Terpenoids from of Euphorbia helioscopia L. with anti-Zika virus activity

inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.11.063openalex-snapshot

Phytochemical and cytotoxic studies on the roots of Euphorbia fischeriana

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1016/j.carbpol.2012.02.004openalex-snapshot

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

inferred← citeshttps://doi.org/10.1016/j.cclet.2019.07.068openalex-snapshot

Euphoractone, a cytotoxic meroterpenoid with an unusual ent-abietane-phloroglucinol skeleton, from Euphorbia fischeriana Steud.

inferred← citeshttps://doi.org/10.1016/j.chempr.2018.10.002openalex-snapshot

Total Synthesis of (±)-Prostratin

inferred← citeshttps://doi.org/10.1016/j.fitote.2011.10.020openalex-snapshot

Comparative characteristic of the inflammatory diterpenes in the roots of Euphorbia fischeriana with different preparation method using HPLC–ELSD

inferred← citeshttps://doi.org/10.1016/j.fitote.2013.09.003openalex-snapshot

Four new diterpenoids from the roots of Euphorbia fischeriana

inferred← citeshttps://doi.org/10.1016/j.fitote.2017.12.006openalex-snapshot

Four new compounds from the roots of Euphorbia ebracteolata and their inhibitory effect on LPS-induced NO production

inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106171openalex-snapshot

Three new diterpenoids from the roots of Euphorbia fischeriana and their cytotoxicity

inferred← citeshttps://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

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1016/j.intimp.2014.06.002openalex-snapshot

HJB-1, a 17-hydroxy-jolkinolide B derivative, inhibits LPS-induced inflammation in mouse peritoneal macrophages

inferred← citeshttps://doi.org/10.1016/j.jep.2013.01.007openalex-snapshot

12-Deoxyphorbol 13-palmitate inhibit VEGF-induced angiogenesis via suppression of VEGFR-2-signaling pathway

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.jpba.2017.12.051openalex-snapshot

Chemical profiling of Euphorbia fischeriana Steud. by UHPLC-Q/TOF-MS

inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2019.111705openalex-snapshot

Gold nanoparticles synthesized from Euphorbia fischeriana root by green route method alleviates the isoprenaline hydrochloride induced myocardial infarction in rats

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.2023.113923openalex-snapshot

Diverse terpenoid glycosides with in vitro cytotoxicity from Glechoma longituba

inferred← citeshttps://doi.org/10.1016/j.phytol.2011.12.011openalex-snapshot

LC–MS method for detecting prostratin in plant extracts and identification of a high-yielding population of Euphorbia fischeriana

inferred← citeshttps://doi.org/10.1016/j.tet.2008.09.019openalex-snapshot

A tandem Baylis–Hillman-singlet oxygen oxidation reaction for facile synthesis of γ-substituted γ-hydroxybutenolides

inferred← citeshttps://doi.org/10.1016/j.tet.2009.03.014openalex-snapshot

Isolation and structure determination of new 4,12-dideoxyphorbol esters from Euphorbia pannonica Host.

inferred← citeshttps://doi.org/10.1016/s1875-5364(09)60008-xopenalex-snapshot

Natural Products Chemistry Research 2006's Progress in China

inferred← citeshttps://doi.org/10.1016/s1875-5364(12)60061-2openalex-snapshot

Chemical constituents of Euphorbia fischeriana

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.jmedchem.0c01449openalex-snapshot

Development of Potential Antitumor Agents from the Scaffolds of Plant-Derived Terpenoid Lactones

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00789openalex-snapshot

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

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00786openalex-snapshot

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

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b01096openalex-snapshot

Inflammation Modulatory Phorbol Esters from the Seeds of Aquilaria malaccensis

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00251openalex-snapshot

Tri- and Diterpenoids from Stillingia loranthacea as Inhibitors of Zika Virus Replication

inferred← citeshttps://doi.org/10.1021/acs.joc.0c00022openalex-snapshot

Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol

inferred← citeshttps://doi.org/10.1021/cr078350sopenalex-snapshot

Chemical and Pharmacological Research of the Plants in Genus Euphorbia

inferred← citeshttps://doi.org/10.1021/cr200397nopenalex-snapshot

Tigliane Diterpenoids from the Euphorbiaceae and Thymelaeaceae Families

inferred← citeshttps://doi.org/10.1021/np0705211openalex-snapshot

Diterpenoids from the Roots of Suregada glomerulata

inferred← citeshttps://doi.org/10.1021/np100673sopenalex-snapshot

Unusual Tigliane Diterpenes from Euphorbia grandicornis

inferred← citeshttps://doi.org/10.1021/np200058copenalex-snapshot

Tigliane-Type Diterpenoid Glycosides from Euphorbia fischeriana

inferred← citeshttps://doi.org/10.1021/np300832nopenalex-snapshot

Cytotoxic Phorbol Esters of Croton tiglium

inferred← citeshttps://doi.org/10.1039/b705951popenalex-snapshot

Diterpenoids

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/c9ob00649dopenalex-snapshot

TiCl 4 - n -Bu 3 N-mediated cascade annulation of ketones with α-ketoesters: a facile synthesis of highly substituted fused γ-alkylidene-butenolides

inferred← citeshttps://doi.org/10.1039/d1qo01312bopenalex-snapshot

Catalytic radical cascade cyclization of alkene-tethered enones to fused bicyclic cyclopropanols

inferred← citeshttps://doi.org/10.1042/bsr20181707openalex-snapshot

The role of chamaejasmine in cellular apoptosis and autophagy in MG-63 cells

inferred← citeshttps://doi.org/10.1080/10286020.2010.512007openalex-snapshot

Isolation and characterization of cytotoxic compounds fromEuphorbia cornigeraBoiss.

inferred← citeshttps://doi.org/10.1080/10286020.2010.532490openalex-snapshot

Diterpenoids from the roots ofEuphorbia fischeriana

inferred← citeshttps://doi.org/10.1080/10286020.2015.1039998openalex-snapshot

Two new diterpenes from the seeds ofCaesalpinia minaxHance

inferred← citeshttps://doi.org/10.1080/10286020.2017.1367923openalex-snapshot

Diterpenoids from the roots of Euphorbia fischeriana and their inhibitory effects on α-glucosidase

inferred← citeshttps://doi.org/10.1080/14786419.2015.1045904openalex-snapshot

Two new ent-atisanes from the root of Euphorbia fischeriana Steud.

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/10.1080/14786419.2021.2003796openalex-snapshot

Euphorfinoids A and B, a pair of ent-atisane diterpenoid epimers from the roots of Euphorbia fischeriana, and their bioactivities

inferred← citeshttps://doi.org/10.1080/14786419.2022.2158463openalex-snapshot

Antiplasmodial and antimicrobial activities of e nt -abietane diterpenoids from the roots of Suregada zanzibariensis

inferred← citeshttps://doi.org/10.1080/23308249.2020.1712325openalex-snapshot

Medicinal Herbs and Plants: Potential Treatment of Monogenean Infections in Fish

inferred← citeshttps://doi.org/10.1097/md.0000000000035118openalex-snapshot

Analysis of the mechanism of action of Euphorbia fischeriana Steud on cirrhosis based on network pharmacology

inferred← citeshttps://doi.org/10.1155/2021/3829434openalex-snapshot

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/10.1158/0008-5472.can-09-0462openalex-snapshot

17-Hydroxy-jolkinolide B Inhibits Signal Transducers and Activators of Transcription 3 Signaling by Covalently Cross-Linking Janus Kinases and Induces Apoptosis of Human Cancer Cells

inferred← citeshttps://doi.org/10.1158/1535-7163.mct-08-0263openalex-snapshot

17-Acetoxyjolkinolide B irreversibly inhibits IκB kinase and induces apoptosis of tumor cells

inferred← citeshttps://doi.org/10.1186/1471-2164-12-600openalex-snapshot

De novo assembly of Euphorbia fischeriana root transcriptome identifies prostratin pathway related genes

inferred← citeshttps://doi.org/10.1201/b12527-15openalex-snapshot

Advances in Medicinal Plants with Antitumoral Activity

inferred← citeshttps://doi.org/10.1201/b12527-18openalex-snapshot

Recent Advances to Evaluate Anti-Diabetic Medicinal Plants

inferred← citeshttps://doi.org/10.14258/jcprm.2020035628openalex-snapshot

ISOLATION AND IDENTIFICATION OF EUPHORBIA TRIODONTA PLANT POLYPHENOLS BY CHROMATO-MASS SPECTROMETRY

inferred← citeshttps://doi.org/10.1590/s0102-695x2011005000096openalex-snapshot

The crude latex of Euphorbia tirucalli modulates the cytokine response of leukocytes, especially CD4+ T lymphocytes

inferred← citeshttps://doi.org/10.3389/fcimb.2017.00456openalex-snapshot

E. fischeriana Root Compound Dpo Activates Antiviral Innate Immunity

inferred← citeshttps://doi.org/10.3390/molecules14114454openalex-snapshot

13C-NMR Data of Three Important Diterpenes Isolated from Euphorbia Species

inferred← citeshttps://doi.org/10.3390/molecules16010466openalex-snapshot

Feeding Deterrents against Two Grain Storage Insects from Euphorbia fischeriana

inferred← citeshttps://doi.org/10.3390/molecules22091524openalex-snapshot

Development of a Matrix Solid-Phase Dispersion Extraction Combined with UPLC/Q-TOF-MS for Determination of Phenolics and Terpenoids from the Euphorbia fischeriana

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/molecules27134282openalex-snapshot

Chemical Composition, Anti-Breast Cancer Activity and Extraction Techniques of Ent-Abietane Diterpenoids from Euphorbia fischeriana Steud

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/10.3724/sp.j.1009.2010.00101openalex-snapshot

Diterpenes and Triterpenes from the Roots of Euphorbia fischeriana

inferred← citeshttps://doi.org/10.3724/sp.j.1009.2012.00299openalex-snapshot

Chemical constituents of Euphorbia fischeriana

inferred← citeshttps://doi.org/10.3892/etm.2016.3061openalex-snapshot

Euphorbia fischeriana Steud inhibits malignant melanoma via modulation of the phosphoinositide-3-kinase/Akt signaling pathway

inferred← citeshttps://doi.org/10.3892/ol.2015.3310openalex-snapshot

Anti-metastatic effect of jolkinolide B and the mechanism of activity in breast cancer MDA-MB-231 cells

inferred← citeshttps://doi.org/10.3892/or.2012.2113openalex-snapshot

Jolkinolide B induces apoptosis in MCF-7 cells through inhibition of the PI3K/Akt/mTOR signaling pathway

inferred← citeshttps://doi.org/10.3892/or.2014.3682openalex-snapshot

Ethyl gallate suppresses proliferation and invasion in human breast cancer cells via Akt-NF-κB signaling

inferred← citeshttps://doi.org/10.5376/mpr.2012.02.0001openalex-snapshot

Casbene Synthase Gene Cloned from Euphorbia fischeriana Steud.

inferred← citeshttps://doi.org/10.5772/intechopen.1010654openalex-snapshot

Phorbol Esters in the Euphorbiaceae Family (Croton, Euphorbia, and Sapium)

inferred← citeshttps://doi.org/10.5897/ajpp11.180openalex-snapshot

In vitro cytotoxic screening of 300 selected Chinese medicinal herbs against human gastric adenocarcinoma SGC-7901 cells

inferred← citeshttps://doi.org/10.5897/ajpp2014.4162openalex-snapshot

Phytochemical profile, antibacterial, antioxidant and cytotoxicity activities of Euphorbia cotinifolia

inferred← citeshttps://doi.org/10.5897/jmpr11.1096openalex-snapshot

Cytotoxic activities of some selected medicinal plants of the genus Euphorbia

inferred← citeshttps://doi.org/10.7150/ijbs.85158openalex-snapshot

IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors

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