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Terpenes from Euphorbia antiquorum and Their in Vitro Anti‐ HIV Activity
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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/oms.1210201102openalex-snapshot
McLafferty reactions in even‐electron ions?
inferredcites →https://doi.org/10.1016/0031-9422(89)80049-4openalex-snapshot
A diterpene from Euphorbia antiquorum
inferredcites →https://doi.org/10.1016/0031-9422(90)80134-3openalex-snapshot
Constituents of the latex of Euphorbia antiquorum
inferredcites →https://doi.org/10.1016/0031-9422(95)00765-2openalex-snapshot
Antibacterial hydroperoxysterols from Xanthosoma robustum
inferredcites →https://doi.org/10.1016/0040-4039(84)80128-8openalex-snapshot
Five ingol esters and a 17-hydroxyingenol ester from the latex of . Assignment of esters using 13C.N.M.R. methods.
inferredcites →https://doi.org/10.1016/s0031-9422(00)00165-5openalex-snapshot
Constituents of various wood-rotting basidiomycetes
inferredcites →https://doi.org/10.1016/s0031-9422(97)01065-0openalex-snapshot
Ingenane and lathyrane diterpenes from the latex of euphorbia acrurensis
inferredcites →https://doi.org/10.1016/s0305-1978(02)00174-6openalex-snapshot
Diterpenes from the latex of Euphorbia nivulia
inferredcites →https://doi.org/10.1021/acsmedchemlett.5b00339openalex-snapshot
Aloperine and Its Derivatives as a New Class of HIV-1 Entry Inhibitors
inferredcites →https://doi.org/10.1021/cr078350sopenalex-snapshot
Chemical and Pharmacological Research of the Plants in Genus Euphorbia
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/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/np0205396openalex-snapshot
Euphane and Tirucallane Triterpenes from the Roots of Euphorbia kansui and Their in Vitro Effects on the Cell Division of Xenopus
inferredcites →https://doi.org/10.1021/np5002237openalex-snapshot
Ingol-Type Diterpenes from Euphorbia antiquorum with Mouse 11β-Hydroxysteroid Dehydrogenase Type 1 Inhibition Activity
inferredcites →https://doi.org/10.1021/np5004752openalex-snapshot
Eurifoloids A–R, Structurally Diverse Diterpenoids from Euphorbia neriifolia
inferredcites →https://doi.org/10.1021/np800816nopenalex-snapshot
Ingol and Ingenol Diterpenes from the Aerial Parts of Euphorbia royleana and Their Antiangiogenic Activities
inferredcites →https://doi.org/10.1021/np900305jopenalex-snapshot
Chemical Constituents of the Roots of Euphorbia micractina
inferredcites →https://doi.org/10.1055/s-0029-1234578openalex-snapshot
Diterpenoids with antitumor activity from Euphorbia esula L.
inferredcites →https://doi.org/10.1055/s-2006-960208openalex-snapshot
New Diterpenoids fromEuphorbia sieboldiana
inferredcites →https://doi.org/10.1080/14786419.2015.1012717openalex-snapshot
A new labdane diterpene from the rhizomes of Alpinia officinarum
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
inferredcites →https://doi.org/10.1248/cpb.37.1547openalex-snapshot
Four ingol type diterpenes from Euphorbia antiquorum L.
inferredcites →https://doi.org/10.3390/molecules171011826openalex-snapshot
Inhibition of 11b-HSD1 by Tetracyclic Triterpenoids from Euphorbia kansui
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.2021.112775zenodo-depositor-declared
Ingenane and jatrophane-type diterpenoids from Euphorbia kansui with multidrug resistance reversal activity
inferred← citeshttps://doi.org/10.1002/cbdv.201900495openalex-snapshot
Diterpenoids from Euphorbia neriifolia and Their Related Anti‐HIV and Cytotoxic Activity
inferred← citeshttps://doi.org/10.1002/cbdv.202301061openalex-snapshot
Terpenoids from Euphorbia helioscopia and Their Cytotoxic Activities against H1975 Cells
inferred← citeshttps://doi.org/10.1002/cbdv.202500736openalex-snapshot
Eupholine A and B, A Pair of Lathyrane Epimers with Inhibitory Activity of Fibrinogen from Euphorbia helioscopia L.
inferred← citeshttps://doi.org/10.1007/s10600-020-02948-wopenalex-snapshot
Diterpenoids from the Seeds of Euphorbia lathyris and their in Vitro Anti-HIV Activity
inferred← citeshttps://doi.org/10.1016/b978-0-443-18866-4.00009-2openalex-snapshot
Antiviral history and viral targets for antiviral therapy
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105296openalex-snapshot
Structurally diverse diterpenoids from the roots of Euphorbia fischeriana Steud
inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107454openalex-snapshot
Euphiquorins A-E, five new structurally diverse diterpenoids from Euphorbia antiquorum L.
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2018.09.206openalex-snapshot
Isolation and characterization of a galactose-specific lectin (EantH) with antimicrobial activity from Euphorbia antiquorum L. latex
inferred← citeshttps://doi.org/10.1016/j.jtcme.2019.08.002openalex-snapshot
HIV-1 protease and reverse transcriptase inhibition by tiger milk mushroom (Lignosus rhinocerus) sclerotium extracts: In vitro and in silico studies
inferred← citeshttps://doi.org/10.1016/j.micpath.2025.107625openalex-snapshot
Harnessing nanotechnology in HIV therapy: Exploring molecular pathogenesis and treatment strategies with special reference to chemotherapy and immunotherapy
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112373openalex-snapshot
Bioactive ent-isopimarane diterpenoids from Euphorbia neriifolia
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112846openalex-snapshot
Diterpenoids from the genus Euphorbia: Structure and biological activity (2013–2019)
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.phytochem.2024.113996openalex-snapshot
Ent-atisane diterpenoids from Euphorbia wallichii and their anti-influenza A virus activity
inferred← citeshttps://doi.org/10.1016/j.phytol.2019.09.003openalex-snapshot
Six new ent-abietane-type diterpenoids from the stem bark of Euphorbia neriifolia
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00087openalex-snapshot
Synthesis of Thioloformate-Containing Lathyrane Diterpene Derivates via a [3,3] Sigmatropic Rearrangement and Their Anti-HIV Activity
inferred← citeshttps://doi.org/10.1039/d0np00039fopenalex-snapshot
ent -Atisane diterpenoids: isolation, structure and bioactivity
inferred← citeshttps://doi.org/10.1039/d2np00047dopenalex-snapshot
Euphorbia diterpenoids: isolation, structure, bioactivity, biosynthesis, and synthesis (2013–2021)
inferred← citeshttps://doi.org/10.1080/14786419.2020.1789634openalex-snapshot
New diterpenoids from the stems of Euphorbia antiquorum growing in Vietnam
inferred← citeshttps://doi.org/10.25259/ajc_253_2026openalex-snapshot
Ent-abietane diterpenoid Enantiomers from Euphorbia helioscopia inhibits liver fibrosis via suppressing the TGF-β1/smad pathway
inferred← citeshttps://doi.org/10.3390/molecules25174019openalex-snapshot
A Review of the Ethnomedicinal Uses, Biological Activities, and Triterpenoids of Euphorbia Species
inferred← citeshttps://doi.org/10.3390/molecules26082257openalex-snapshot
Alpha-Glucosidase Inhibitory Diterpenes from Euphorbia antiquorum Growing in Vietnam
inferred← citeshttps://doi.org/10.57634/rcr5056openalex-snapshot
Antiviral properties of diterpenes and their derivatives
inferred← citeshttps://doi.org/10.5772/intechopen.1010654openalex-snapshot
Phorbol Esters in the Euphorbiaceae Family (Croton, Euphorbia, and Sapium)
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