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Fischdiabietane A, an Antitumoral Diterpenoid Dimer Featuring an Unprecedented Carbon Skeleton from 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/10.1002/anie.201700838openalex-snapshot
Bioinspired Asymmetric Synthesis of Hispidanin A
inferredcites →https://doi.org/10.1002/anie.201700958openalex-snapshot
Asymmetric Total Synthesis of Hispidanin A
inferredcites →https://doi.org/10.1002/chem.201801156openalex-snapshot
Asymmetric Synthesis of Hispidanin A and Related Diterpenoids
inferredcites →https://doi.org/10.1002/hlca.201200092openalex-snapshot
Bisyinshanic Acids A and B, Two Novel Diterpene Dimers from the Roots of Euphorbia yinshanica
inferredcites →https://doi.org/10.1016/s0040-4039(02)02505-4openalex-snapshot
Langduin C, a novel dimeric diterpenoid from the roots of Euphorbia fischeriana
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00595openalex-snapshot
Heterodimeric Diterpenoids Isolated fromEuphorbia ebracteolataRoots and Their Inhibitory Effects on α-Glucosidase
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00909openalex-snapshot
Modified Abietane Diterpenoids from Whole Plants of Selaginella moellendorffii
inferredcites →https://doi.org/10.1021/acs.orglett.0c00898openalex-snapshot
Terpenoids from Resina Commiphora Regulating Lipid Metabolism via Activating PPARα and CPT1 Expression
inferredcites →https://doi.org/10.1021/acs.orglett.6b03597openalex-snapshot
Taxodikaloids A and B, Two Dimeric Abietane-Type Diterpenoids from Taxodium ascendens Possessing an Oxazoline Ring Linkage
inferredcites →https://doi.org/10.1021/acs.orglett.9b03133openalex-snapshot
Alterbrassinoids A–D: Fusicoccane-Derived Diterpenoid Dimers Featuring Different Carbon Skeletons from Alternaria brassicicola
inferredcites →https://doi.org/10.1021/cr078350sopenalex-snapshot
Chemical and Pharmacological Research of the Plants in Genus Euphorbia
inferredcites →https://doi.org/10.1021/cr400541jopenalex-snapshot
Euphorbia Diterpenes: Isolation, Structure, Biological Activity, and Synthesis (2008–2012)
inferredcites →https://doi.org/10.1021/ol501417kopenalex-snapshot
Hispidanins A–D: Four New Asymmetric Dimeric Diterpenoids from the Rhizomes of Isodon hispida
inferredcites →https://doi.org/10.1038/s41598-017-14637-wopenalex-snapshot
Two novel diterpenoid heterodimers, Bisebracteolasins A and B, from Euphorbia ebracteolata Hayata, and the cancer chemotherapeutic potential of Bisebracteolasin A
inferredcites →https://doi.org/10.1039/c7ra11982hopenalex-snapshot
Ent -abietane diterpenoids and their probable biogenetic precursors from the roots of Euphorbia fischeriana
inferredcites →https://doi.org/10.1039/c8qo01379aopenalex-snapshot
Fischernolides A–D, four novel diterpene-based meroterpenoid scaffolds with antitumor activities from Euphorbia fischeriana
inferredcites →https://doi.org/10.1039/c9np00037bopenalex-snapshot
Naturally occurring [4 + 2] type terpenoid dimers: sources, bioactivities and total syntheses
inferredcites →https://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
inferredcites →https://doi.org/10.1055/s-0042-114573openalex-snapshot
Naturally Occurring Diterpenoid Dimers: Source, Biosynthesis, Chemistry and Bioactivities
inferredcites →https://doi.org/10.1080/10286020500480308openalex-snapshot
Yuexiandajisu D, a novel 18-nor-rosane-type dimeric diterpenoid fromEuphorbiaebracteolataHayata
inferredcites →https://doi.org/10.2147/dddt.s210220openalex-snapshot
Aucubin Protects Chondrocytes Against IL-1β-Induced Apoptosis In Vitro And Inhibits Osteoarthritis In Mice Model
inferredcites →https://doi.org/10.2174/1389557516666160923130814openalex-snapshot
ent-Abietane Lactones from Euphorbia
inferredcites →https://doi.org/10.3390/molecules23020387openalex-snapshot
Anti-Cancer Activities of Diterpenoids Derived from Euphorbia fischeriana Steud
inferredcites →https://doi.org/10.3390/molecules23040935openalex-snapshot
Structural Diversity and Biological Activities of Diterpenoids Derived from Euphorbia fischeriana Steud
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.2022.113304zenodo-depositor-declared
Diverse gallotannins with α-glucosidase and α-amylase inhibitory activity from the roots of Euphorbia fischeriana steud.
inferred← citeshttps://doi.org/10.1002/cbdv.202400808openalex-snapshot
Abietane‐Type Diterpenoids: Insights into Structural Diversity and Therapeutic Potential
inferred← citeshttps://doi.org/10.1002/cjoc.202300275openalex-snapshot
Natural Sesquiterpenoids, Diterpenoids, Sesterterpenoids, and Triterpenoids with Intriguing Structures from 2017 to 2022
inferred← citeshttps://doi.org/10.1002/cjoc.202400697openalex-snapshot
Recent Advances of Terpenoids with Intriguing Chemical Skeletons and Biological Activities
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_3openalex-snapshot
Classification of Diverse Novel Diterpenoids
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.
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.2022.115574openalex-snapshot
Phytochemical and pharmacological review of diterpenoids from the genus Euphorbia Linn (2012–2021)
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113784openalex-snapshot
Yuexiandajisu diterpenoids from Euphorbia ebracteolata Hayata (Langdu roots): An overview
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00580openalex-snapshot
Diterpenoids from Euphorbia fischeriana with Kv1.3 Inhibitory Activity
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01831openalex-snapshot
Scandium-Catalyzed Skeleton Conversion of Lathyrane to Lathyranone-Type Euphorbia Diterpenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03852openalex-snapshot
Catalytic Enantioselective Synthesis of 2,3-Dihydrobenzo[b]oxepines via Asymmetric Oxetane Opening by Internal Carbon Nucleophiles
inferred← citeshttps://doi.org/10.1039/d2np00039copenalex-snapshot
Biogenetic and biomimetic synthesis of natural bisditerpenoids: hypothesis and practices
inferred← citeshttps://doi.org/10.1039/d2np00047dopenalex-snapshot
Euphorbia diterpenoids: isolation, structure, bioactivity, biosynthesis, and synthesis (2013–2021)
inferred← citeshttps://doi.org/10.1039/d3ob01007dopenalex-snapshot
Discovery of two ent -atisane diterpenoid lactones with AChE inhibitory activity from the roots of Euphorbia fischeriana
inferred← citeshttps://doi.org/10.1080/10286020.2022.2117169openalex-snapshot
Survey of natural products reported by Asian research groups in 2021
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/10.3389/fntpr.2022.1086897openalex-snapshot
Computational methods and points for attention in absolute configuration determination
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