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ent-Rosane diterpenoids from Euphorbia milii showing an Epstein–Barr virus lytic replication assay

https://doi.org/10.1039/c7ra08877a
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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/prac.19973390126openalex-snapshot
Determination of the Absolute Configuration of Chiral 1,3-Diols by CD spectroscopy of their [Mo2(OAc)4] complexes
inferredcites →https://doi.org/10.1007/bf00325835openalex-snapshot
Chiroptical properties of steroid 1,3-diaxial diols in the presence of [Mo2(OAc)4]
inferredcites →https://doi.org/10.1007/s00044-017-1937-3openalex-snapshot
Labdane diterpene lactones of Vitex pubescens and their antileukemic properties
inferredcites →https://doi.org/10.1007/s13659-015-0055-5openalex-snapshot
New Diterpenes from Cultures of the Fungus Engleromyces goetzii and Their CETP Inhibitory Activity
inferredcites →https://doi.org/10.1016/0304-3835(81)90066-5openalex-snapshot
Combined effect of the extracts from Croton tiglium, Euphorbia lathyris or Euphorbia tirucalli and n-butyrate on Epstein-Barr virus expression in human lymphoblastoid P3HR-1 and Raji cells
inferredcites →https://doi.org/10.1016/j.antiviral.2014.05.003openalex-snapshot
Antiviral activity of topoisomerase II catalytic inhibitors against Epstein–Barr virus
inferredcites →https://doi.org/10.1016/j.phytochem.2009.10.005openalex-snapshot
Effects of diterpenes from latex of Euphorbia lactea and Euphorbia laurifolia on human immunodeficiency virus type 1 reactivation
inferredcites →https://doi.org/10.1016/s0031-9422(00)90437-0openalex-snapshot
Ent-14β-hydroxy-8(17),12-labdadien-16,15-olide-3β,19-oxide: A diterpene from the aerial parts of Andrographis paniculata
inferredcites →https://doi.org/10.1016/s0166-3542(96)01004-2openalex-snapshot
Antireplicative and anticytopathic activities of prostratin, a non-tumor-promoting phorbol ester, against human immunodeficiency virus (HIV)1
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b01012openalex-snapshot
Carolignans from the Aerial Parts of Euphorbia sikkimensis and Their Anti-HIV Activity
inferredcites →https://doi.org/10.1021/acs.orglett.6b03142openalex-snapshot
Euphomilones A and B, ent-Rosane Diterpenoids with 7/5/6 and 5/7/6 Skeletons from Euphorbia milii
inferredcites →https://doi.org/10.1021/cr078350sopenalex-snapshot
Chemical and Pharmacological Research of the Plants in Genus Euphorbia
inferredcites →https://doi.org/10.1021/cr200397nopenalex-snapshot
Tigliane Diterpenoids from the Euphorbiaceae and Thymelaeaceae Families
inferredcites →https://doi.org/10.1021/cr400541jopenalex-snapshot
Euphorbia Diterpenes: Isolation, Structure, Biological Activity, and Synthesis (2008–2012)
inferredcites →https://doi.org/10.1021/np010377yopenalex-snapshot
Eupha-7,9(11),24-trien-3β-ol (“Antiquol C”) and Other Triterpenes fromEuphorbiaantiquorumLatex and Their Inhibitory Effects on Epstein−Barr Virus Activation
inferredcites →https://doi.org/10.1021/np400757kopenalex-snapshot
Potential Antiviral Lignans from the Roots of Saururus chinensis with Activity against Epstein–Barr Virus Lytic Replication
inferredcites →https://doi.org/10.1021/np400873vopenalex-snapshot
Anti-inflammatory Diterpenoids from the Roots of Euphorbia ebracteolata
inferredcites →https://doi.org/10.1021/np500988mopenalex-snapshot
neo-Clerodane Diterpenoids from Scutellaria barbata with Activity against Epstein–Barr Virus Lytic Replication
inferredcites →https://doi.org/10.1055/s-2001-17368openalex-snapshot
Cytotoxicities and Anti-Herpes Simplex Virus Activities of Diterpenes Isolated from Euphorbia Species
inferredcites →https://doi.org/10.1055/s-2002-32070openalex-snapshot
Inhibition of HIV-1 Integrase by Galloyl Glucoses from Terminalia chebula and Flavonol Glycoside Gallates from Euphorbia pekinensis
inferredcites →https://doi.org/10.1080/14786410310001605841openalex-snapshot
Evaluation of the Antiviral and Antimicrobial Activities of Triterpenes Isolated fromEuphorbia segetalis
inferredcites →https://doi.org/10.1093/jac/dkh136openalex-snapshot
Putranjivain A from Euphorbia jolkini inhibits both virus entry and late stage replication of herpes simplex virus type 2 in vitro
inferredcites →https://doi.org/10.1111/j.1440-1681.2005.04194.xopenalex-snapshot
EUPHORBIA THYMIFOLIA SUPPRESSES HERPES SIMPLEX VIRUS‐2 INFECTION BY DIRECTLY INACTIVATING VIRUS INFECTIVITY

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.2022.113106zenodo-depositor-declared
Diverse diterpenoids with α-glucosidase and β-glucuronidase inhibitory activities from Euphorbia milii
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/10.1002/cbdv.202300013openalex-snapshot
New Rosane Diterpenoids and Their Analogs from Euphorbia ebracteolata Hayata
inferred← citeshttps://doi.org/10.1002/cjoc.202400749openalex-snapshot
Skeleton Rearranged and Oxygenated ent ‐Rosane Diterpenoids with Antiadipogenic Activity from Euphorbia milii
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107253openalex-snapshot
Identification and structural modification of ent-rosane diterpenoids from Euphorbia milii inhibiting RANKL-induced osteoclastogenesis
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.02.028openalex-snapshot
Triterpenoids from Euphorbia pulcherrima with inhibitory effects on osteoclastogenesis
inferred← citeshttps://doi.org/10.1016/j.jep.2026.121772openalex-snapshot
Traditional Herbal Medicine Euphorbia milii Des Moul: Research progress in chemical constituents and pharmacological activities
inferred← citeshttps://doi.org/10.1016/j.phymed.2024.155634openalex-snapshot
Anticancer diterpenes of African natural products: Mechanistic pathways and preclinical developments
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114934openalex-snapshot
Structurally diverse diterpenoids from Euphorbia milii: Discovery and RORγt-binding evaluation
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114947openalex-snapshot
Terpenoids in Euphorbia milii Ch. des Moulins and their anti-rheumatic potential
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00929openalex-snapshot
Jatrophane Diterpenoids from Euphorbia esula as Inhibitors of RANKL-Induced Osteoclastogenesis
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03935openalex-snapshot
Fluvirosaones A and B, Two Indolizidine Alkaloids with a Pentacyclic Skeleton from Flueggea virosa
inferred← citeshttps://doi.org/10.1039/c8np00079dopenalex-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/10.1039/d3cy00115fopenalex-snapshot
Harnessing the catalytic plasticity of the ent -kaurene synthase from Bradyrhizobium japonicum to produce the ent -rosane and ent -pimarane scaffolds
inferred← citeshttps://doi.org/10.1080/14786419.2021.1948846openalex-snapshot
A new ingol diterpenoid from the seeds of Euphorbia marginata Pursh
inferred← citeshttps://doi.org/10.1186/s43094-026-00945-4openalex-snapshot
Therapeutic potential of rutamarin: preclinical evidence of its biological properties through in silico, in vitro, and in vivo studies
inferred← citeshttps://doi.org/10.1248/cpb.c22-00648openalex-snapshot
Omphalines A–E: ent-Rosane-Type Diterpenoids from the Madagascar Endemic Plant, Omphalea oppositifolia
inferred← citeshttps://doi.org/10.3390/ijms24021716openalex-snapshot
The Fight against the Carcinogenic Epstein-Barr Virus: Gut Microbiota, Natural Medicines, and Beyond
inferred← citeshttps://doi.org/10.3390/molecules26165055openalex-snapshot
Euphorbia Diterpenes: An Update of Isolation, Structure, Pharmacological Activities and Structure–Activity Relationship
inferred← citeshttps://doi.org/10.52711/0974-360x.2023.00507openalex-snapshot
Antiangiogenic activity and the isolation of five phenolic compounds from Euphorbia milii ethyl acetate solvent extract
inferred← citeshttps://doi.org/10.5599/admet.3165openalex-snapshot
Rosanoid diterpenoids: structural diversity, classification and biological activities
inferred← citeshttps://doi.org/10.57634/rcr5056openalex-snapshot
Antiviral properties of diterpenes and their derivatives
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