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Quorumolides A–C, Three Cembranoids from Euphorbia antiquorum

https://doi.org/10.1021/acs.joc.7b02684

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/0031-9422(90)80134-3openalex-snapshot

Constituents of the latex of Euphorbia antiquorum

inferredcites →https://doi.org/10.1016/0031-9422(90)85373-nopenalex-snapshot

Revised structure of a diterpene from Euphorbia antiquorum

inferredcites →https://doi.org/10.1016/0960-894x(96)00142-4openalex-snapshot

A cembranolide diterpene farnesyl protein transferase inhibitor from the marine soft coral Lobophytum cristagalli

inferredcites →https://doi.org/10.1016/j.bmcl.2005.11.071openalex-snapshot

Protein tyrosine phosphatase 1B inhibitors from Morus root bark

inferredcites →https://doi.org/10.1016/j.fitote.2013.07.004openalex-snapshot

A new cytotoxic cembrane diterpene from the roots of Euphorbia pekinensis Rupr

inferredcites →https://doi.org/10.1016/j.phytochem.2006.06.030openalex-snapshot

Chemistry and biological activity of secondary metabolites in Euphorbia from Iran

inferredcites →https://doi.org/10.1016/j.tet.2004.09.108openalex-snapshot

Antiplasmodial cembradiene diterpenoids from a Southwestern Caribbean gorgonian octocoral of the genus Eunicea

inferredcites →https://doi.org/10.1016/j.tet.2008.07.104openalex-snapshot

Durumolides A–E, anti-inflammatory and antibacterial cembranolides from the soft coral Lobophytum durum

inferredcites →https://doi.org/10.1016/j.tet.2010.06.094openalex-snapshot

Steroid and cembranoids from the Dongsha atoll soft coral Lobophytum sarcophytoides

inferredcites →https://doi.org/10.1016/j.tetlet.2011.03.023openalex-snapshot

Cembradienes from the Caribbean sea whip Eunicea sp.

inferredcites →https://doi.org/10.1021/jf401303qopenalex-snapshot

Cembranoids from the Soft Coral Sinularia rigida with Antifouling Activities

inferredcites →https://doi.org/10.1021/np100044topenalex-snapshot

Lactonecembranoids from Croton laevigatus

inferredcites →https://doi.org/10.1021/np2002012openalex-snapshot

Cembranolides from the Leaves of Croton gratissimus

inferredcites →https://doi.org/10.1021/np300313kopenalex-snapshot

Disruption in Quorum-Sensing Systems and Bacterial Biofilm Inhibition by Cembranoid Diterpenes Isolated from the Octocoral Eunicea knighti

inferredcites →https://doi.org/10.1021/np300636kopenalex-snapshot

Clerodane Diterpenoids from Croton crassifolius

inferredcites →https://doi.org/10.1021/np400260gopenalex-snapshot

11β-HSD1 Inhibitors from Walsura cochinchinensis

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/np900693ropenalex-snapshot

Cembranoids from the Octocoral Sarcophyton ehrenbergi

inferredcites →https://doi.org/10.1021/ol050206aopenalex-snapshot

Lathyranoic Acid A: First Secolathyrane Diterpenoid in Nature fromEuphorbia lathyris

inferredcites →https://doi.org/10.1093/jnci/82.13.1107openalex-snapshot

New Colorimetric Cytotoxicity Assay for Anticancer-Drug Screening

inferredcites →https://doi.org/10.1248/cpb.37.1547openalex-snapshot

Four ingol type diterpenes from Euphorbia antiquorum L.

inferredcites →https://doi.org/10.2174/138527212800672583openalex-snapshot

Cembrane Diterpenes Chemistry and Biological Properties

inferredcites →https://doi.org/10.3390/md8112848openalex-snapshot

Lobophytones O–T, New Biscembranoids and Cembranoid from Soft Coral Lobophytum pauciflorum

inferredcites →https://doi.org/10.4161/cbt.6.5.3960openalex-snapshot

Caspase-8 preferentially senses the apoptosis-inducing action of NG-18, A gambogic acid derivative, in human leukemia HL-60 cells

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/10.1002/ajoc.201800517openalex-snapshot

DABCO‐Mediated C−O Bond Formation from Csp2‐Halogen Bond‐Containing Compounds and Alkyl Alcohols

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.2019.103292openalex-snapshot

Discovery of diverse diterpenoid scaffolds from Euphorbia antiquorum and their activity against RANKL-induced osteoclastogenesis

inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106619openalex-snapshot

Diterpenoids with an unusual tricyclo[10.3.0.02,9]pentadecane skeleton from Pedilanthus tithymaloides as multidrug resistance modulators

inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108961openalex-snapshot

Tigliane glycosides from Euphorbia tirucalli as multidrug resistance modulators

inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104699openalex-snapshot

Bioactive cembrane diterpenoids from the gum resin of Boswellia carterii

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.nexres.2026.102321openalex-snapshot

Euphorbia royleana Boiss., as a source of bioactive compounds: Traditional uses and pharmacological evidence

inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112395openalex-snapshot

Diterpenoids from Euphorbia royleana reverse P-glycoprotein-mediated multidrug resistance in cancer cells

inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114233openalex-snapshot

Lathyrane diterpenoids with multidrug resistance reversal activity from the tubers of Euphorbia antiquorum

inferred← citeshttps://doi.org/10.1021/acs.jafc.5c11512openalex-snapshot

Genome Mining Guided Discovery of Macrocyclic Sesterterpenoids with Anti-MRSA and Anti-Neuroinflammatory Activities

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00134openalex-snapshot

Bioactive Diterpenoids from the Stems of Euphorbia antiquorum

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00519openalex-snapshot

Macrocyclic Diterpenoids from Euphorbia helioscopia and Their Potential Anti-inflammatory Activity

inferred← citeshttps://doi.org/10.1021/acs.joc.6c01073openalex-snapshot

Cascade Construction of Cinnoline and Furanone Skeletons from Phenylhydrazine and Maleimide Featuring a Formal Oxygen Swap

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01114openalex-snapshot

Pepluanols C–D, Two Diterpenoids with Two Skeletons from Euphorbia peplus

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02363openalex-snapshot

Rapid Construction of the Scaffold of Quorumolide A Enabled by a Tandem ROM/RCM Strategy and a Tandem Oxidative Cyclization Strategy

inferred← citeshttps://doi.org/10.1039/c9gc01811eopenalex-snapshot

A copper-catalyzed diastereoselective O-transfer reaction of N -vinyl-α,β-unsaturated nitrones with ketenes into γ-lactones through [5 + 2] cycloaddition and N–O bond cleavage

inferred← citeshttps://doi.org/10.1039/c9ra03403jopenalex-snapshot

Quick construction of a C–N bond from arylsulfonyl hydrazides and C sp2 –X compounds promoted by DMAP at room temperature

inferred← citeshttps://doi.org/10.1039/d2np00047dopenalex-snapshot

Euphorbia diterpenoids: isolation, structure, bioactivity, biosynthesis, and synthesis (2013–2021)

inferred← citeshttps://doi.org/10.1039/d3cc05888copenalex-snapshot

Pyridine-catalyzed ring-opening reaction of cyclopropenone with bromomethyl carbonyl compounds toward furan-2(5 H )-ones

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Survey of natural products reported by Asian research groups in 2018

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Diterpenes and sterols from the Red Sea soft coral Sarcophyton trocheliophorum and their cytotoxicity and anti-leishmanial activities

inferred← citeshttps://doi.org/10.1360/ssc-2022-0203openalex-snapshot

The discovery and study of structurally intriguing bioactive natural molecules from medicinal plants: from year 2012 to 2022

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Traditional Uses, Pharmacological, and Phytochemical Studies of Euphorbia: A Review

inferred← citeshttps://doi.org/10.3390/molecules26082257openalex-snapshot

Alpha-Glucosidase Inhibitory Diterpenes from Euphorbia antiquorum Growing in Vietnam

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