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Fischernolides A–D, four novel diterpene-based meroterpenoid scaffolds with antitumor activities 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/10.1002/0470846275openalex-snapshot

Medicinal Natural Products

inferredcites →https://doi.org/10.1002/anie.201708333openalex-snapshot

One‐Step Multigram‐Scale Biomimetic Synthesis of Psiguadial B

inferredcites →https://doi.org/10.1002/chir.20733openalex-snapshot

ECD cotton effect approximated by the Gaussian curve and other methods

inferredcites →https://doi.org/10.1016/0031-9422(95)00752-0openalex-snapshot

Diterpenes and phloracetophenones from Euphorbia portulacoides

inferredcites →https://doi.org/10.1016/j.fitote.2013.09.003openalex-snapshot

Four new diterpenoids from the roots of Euphorbia fischeriana

inferredcites →https://doi.org/10.1016/j.jcyt.2017.03.003openalex-snapshot

Manufacture and preparation of human placenta-derived mesenchymal stromal cells for local tissue delivery

inferredcites →https://doi.org/10.1016/s0031-9422(99)00169-7openalex-snapshot

Diterpenes and aromatic compounds from Euphorbia fischeriana

inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00789openalex-snapshot

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

inferredcites →https://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

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00606openalex-snapshot

Rearranged Phloroglucinol-Monoterpenoid Adducts from Callistemon rigidus

inferredcites →https://doi.org/10.1021/acs.orglett.5b03117openalex-snapshot

Guajavadimer A, a Dimeric Caryophyllene-Derived Meroterpenoid with a New Carbon Skeleton from the Leaves of Psidium guajava

inferredcites →https://doi.org/10.1021/acs.orglett.6b00362openalex-snapshot

Himalensines A and B, Alkaloids from Daphniphyllum himalense

inferredcites →https://doi.org/10.1021/acs.orglett.6b00906openalex-snapshot

Filicinic Acid Based Meroterpenoids with Anti-Epstein–Barr Virus Activities from Hypericum japonicum

inferredcites →https://doi.org/10.1021/acs.orglett.6b01817openalex-snapshot

Meroterpenoids with New Skeletons from Myrtus communis and Structure Revision of Myrtucommulone K

inferredcites →https://doi.org/10.1021/acs.orglett.7b02955openalex-snapshot

Manginoids A–G: Seven Monoterpene–Shikimate-Conjugated Meroterpenoids with a Spiro Ring System from Guignardia mangiferae

inferredcites →https://doi.org/10.1021/acs.orglett.8b00561openalex-snapshot

Commiphoratones A and B, Two Sesquiterpene Dimers from Resina Commiphora

inferredcites →https://doi.org/10.1021/acs.orglett.8b01476openalex-snapshot

Magterpenoids A–C, Three Polycyclic Meroterpenoids with PTP1B Inhibitory Activity from the Bark of Magnolia officinalis var. biloba

inferredcites →https://doi.org/10.1021/acs.orglett.8b02259openalex-snapshot

Eucalyptusdimers A–C, Dimeric Phloroglucinol–Phellandrene Meroterpenoids from Eucalyptus robusta

inferredcites →https://doi.org/10.1021/acsami.6b09542openalex-snapshot

Zinc-Doped Copper Oxide Nanocomposites Inhibit the Growth of Human Cancer Cells through Reactive Oxygen Species-Mediated NF-κB Activations

inferredcites →https://doi.org/10.1021/jacs.6b07229openalex-snapshot

Enantioselective Total Synthesis of (+)-Psiguadial B

inferredcites →https://doi.org/10.1021/np200058copenalex-snapshot

Tigliane-Type Diterpenoid Glycosides from Euphorbia fischeriana

inferredcites →https://doi.org/10.1021/ol102179uopenalex-snapshot

Psiguadials A and B, Two Novel Meroterpenoids with Unusual Skeletons from the Leaves of Psidium guajava

inferredcites →https://doi.org/10.1039/c7ra11982hopenalex-snapshot

Ent -abietane diterpenoids and their probable biogenetic precursors from the roots of Euphorbia fischeriana

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.2020.112519zenodo-depositor-declared

Bond reactivity indices approach analysis of the [2+2] cycloaddition of jatrophane skeleton diterpenoids from Euphorbia gaditana Coss to tetracyclic gaditanone

inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112867zenodo-depositor-declared

Euphorfinoids E-L: Diterpenoids from the roots of Euphorbia fischeriana with acetylcholinesterase inhibitory activity

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113154zenodo-depositor-declared

Characterization of undescribed melanoma inhibitors from Euphorbia mauritanica L. cultivated in Egypt targeting BRAFV600E and MEK 1 kinases via in-silico study and ADME prediction

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/10.1007/978-981-99-7329-3_14openalex-snapshot

Biological Activities

inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_8openalex-snapshot

Classification of Diverse Novel Meroterpenoids

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.bioorg.2021.105395openalex-snapshot

Euphorfistrines A-G, cytotoxic and AChE inhibiting triterpenoids from the roots of Euphorbia fischeriana

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.jep.2021.114095openalex-snapshot

Existing knowledge on Euphorbia fischeriana Steud. (Euphorbiaceae): Traditional uses, clinical applications, phytochemistry, pharmacology and toxicology

inferred← citeshttps://doi.org/10.1021/acs.joc.1c00305openalex-snapshot

Fischdiabietane A, an Antitumoral Diterpenoid Dimer Featuring an Unprecedented Carbon Skeleton from Euphorbia fischeriana

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

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

inferred← citeshttps://doi.org/10.1039/d2ob00053aopenalex-snapshot

Unprecedented diterpenoid dimers with soluble epoxide hydrolase inhibitory effect from Euphorbia fischeriana

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/10.1039/d4ob01548gopenalex-snapshot

Isolation and biomimetic synthesis of acylphloroglucinol meroterpenoids as anti-breast cancer agents from Dryopteris crassirhizoma

inferred← citeshttps://doi.org/10.1080/14786419.2021.2013215openalex-snapshot

Four sesquiterpenoids from the vegetable raw material Schisandra chinensis (Turcz.) Baill.: leaves and stems

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/10.21577/0100-4042.20170932openalex-snapshot

DITERPENOS ENT-ABIETANOS DE Euphorbia phosphorea (EUPHORBIACEAE)

inferred← citeshttps://doi.org/10.3389/fphar.2022.830103openalex-snapshot

Biological activities of meroterpenoids isolated from different sources

inferred← citeshttps://doi.org/10.3390/biom11070957openalex-snapshot

Meroterpenoids: A Comprehensive Update Insight on Structural Diversity and Biology

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/10.3390/molecules28135172openalex-snapshot

Phytochemical Analysis, Antioxidant Activities In Vitro and In Vivo, and Theoretical Calculation of Different Extracts of Euphorbia fischeriana

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