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neo-Clerodane Diterpenoids from Scutellaria barbata with Activity against Epstein–Barr Virus Lytic Replication

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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.200900431openalex-snapshot

Novel Antioxidant neo‐Clerodane Diterpenoids from Scutellaria barbata

inferredcites →https://doi.org/10.1007/s13659-011-0016-6openalex-snapshot

neo-Clerodane diterpenoids from Salvia dugesii and their bioactive studies

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.bmcl.2009.10.116openalex-snapshot

Two novel neo-clerodane diterpenoids from Scutellaria barbata

inferredcites →https://doi.org/10.1016/j.bse.2013.12.012openalex-snapshot

Chemical constituents from the roots of Elephantopus scaber L.

inferredcites →https://doi.org/10.1016/j.fitote.2010.01.001openalex-snapshot

New neo-clerodane diterpenoids from Scutellaria barbata with cytotoxic activities

inferredcites →https://doi.org/10.1016/j.phytochem.2004.02.005openalex-snapshot

Chemical composition and antimicrobial activity of the essential oil of Scutellaria barbata

inferredcites →https://doi.org/10.1016/j.phytochem.2006.04.024openalex-snapshot

neo-Clerodane diterpenoids from Scutellaria barbata with cytotoxic activities

inferredcites →https://doi.org/10.1016/s0378-8741(00)00265-8openalex-snapshot

Phytochemical flavones isolated from Scutellaria barbata and antibacterial activity against methicillin-resistant Staphylococcus aureus

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/np900309popenalex-snapshot

Cytotoxic Neoclerodane Diterpenoids from Scutellaria barbata

inferredcites →https://doi.org/10.1021/np900362zopenalex-snapshot

Cytotoxic neo-Clerodane Diterpenoid Alkaloids from Scutellaria barbata

inferredcites →https://doi.org/10.1038/sj.onc.1210240openalex-snapshot

Epstein–Barr virus infection in humans: from harmless to life endangering virus–lymphocyte interactions

inferredcites →https://doi.org/10.1039/c3ra23172kopenalex-snapshot

Chrysanolide A, an unprecedented sesquiterpenoid trimer from the flowers of Chrysanthemum indicum L

inferredcites →https://doi.org/10.1055/s-0030-1270797openalex-snapshot

Neoclerodane Diterpenoids fromScutellaria barbata

inferredcites →https://doi.org/10.1055/s-2007-990215openalex-snapshot

Bioactive ent-Clerodane Diterpenoids from Scutellaria barbata

inferredcites →https://doi.org/10.1080/10286020.2013.821983openalex-snapshot

Bioassay-guided isolation of neo-clerodane diterpenoids fromScutellaria barbata

inferredcites →https://doi.org/10.1081/iph-200026840openalex-snapshot

Inhibitory Effects ofScutellaria BarbataD. Don. andEuonymus Alatus Sieb. on Aromatase Activity of Human Leiomyomal Cells

inferredcites →https://doi.org/10.1111/j.1744-7909.2008.00672.xopenalex-snapshot

Two New neo‐Clerodane Diterpenoids from Scutellaria barbata

inferredcites →https://doi.org/10.1177/1934578x1100600410openalex-snapshot

Diterpene Lactones with Labdane, Halimane and Clerodane Frameworks

inferredcites →https://doi.org/10.1248/cpb.54.869openalex-snapshot

Four New neo-Clerodane Diterpenoid Alkaloids from Scutellaria barbata with Cytotoxic Activities

inferredcites →https://doi.org/10.1248/cpb.55.1218openalex-snapshot

Five New neo-Clerodane Diterpenoid Alkaloids from Scutellaria barbata with Cytotoxic Activities

inferredcites →https://doi.org/10.1248/cpb.56.207openalex-snapshot

New neo-Clerodane Diterpenoid Alkaloids from Scutellaria barbata with Cytotoxic Activities

inferredcites →https://doi.org/10.1248/cpb.58.1267openalex-snapshot

Scutebarbatines W-Z, New neo-Clerodane Diterpenoids from Scutellaria barbata and Structure Revision of a Series of 13-Spiro neo-Clerodanes

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.2022.113285zenodo-depositor-declared

Diterpenes of Scutellaria spp.: Phytochemistry and pharmacology

inferred← citeshttps://doi.org/10.1002/cbdv.202100693openalex-snapshot

neo ‐Clerodane Diterpenoids from the Aerial Parts of Scutellaria barbata with Anti‐Inflammatory Activity

inferred← citeshttps://doi.org/10.1007/978-981-13-0289-3_6openalex-snapshot

Neuropharmacology of Scutellaria baicalensis Georgi

inferred← citeshttps://doi.org/10.1007/s10600-022-03726-6openalex-snapshot

Chemical Constituents of Hedyotis diffusa and Their Anti-Inflammatory Activity

inferred← citeshttps://doi.org/10.1016/b978-0-443-15589-5.00004-9openalex-snapshot

Progress in the study of natural neo-clerodane diterpenoids

inferred← citeshttps://doi.org/10.1016/j.bioorg.2017.10.008openalex-snapshot

Nitric oxide inhibitors with a spiro diterpenoid skeleton from Scutellaria formosana : Structures, NO inhibitory effects, and interactions with iNOS

inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.02.045openalex-snapshot

New cytotoxic neo-clerodane diterpenoids from Scutellaria strigillosa

inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.05.045openalex-snapshot

neo-Clerodane diterpenoids from Scutellaria barbata mediated inhibition of P-glycoprotein in MCF-7/ADR cells

inferred← citeshttps://doi.org/10.1016/j.fitote.2017.03.012openalex-snapshot

Scubatines A–F, new cytotoxic neo -clerodane diterpenoids from Scutellaria barbata D. Don

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2019.04.055openalex-snapshot

Phytochemical constituents from Scutellaria baicalensis in soluble epoxide hydrolase inhibition: Kinetics and interaction mechanism merged with simulations

inferred← citeshttps://doi.org/10.1016/j.jep.2019.112260openalex-snapshot

A review of the ethnopharmacology, phytochemistry, pharmacology, and quality control of Scutellaria barbata D. Don

inferred← citeshttps://doi.org/10.1016/j.jep.2020.113198openalex-snapshot

Traditional uses, ten-years research progress on phytochemistry and pharmacology, and clinical studies of the genus Scutellaria

inferred← citeshttps://doi.org/10.1016/j.jics.2021.100041openalex-snapshot

A molecular docking study of potential inhibitors and repurposed drugs against SARS-CoV-2 main protease enzyme

inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.09.002openalex-snapshot

Neo-clerodane diterpenoids from the whole plants of Scutellaria formosana

inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.09.005openalex-snapshot

Clerodane diterpenoids from Scutellaria formosana with inhibitory effects on NO production and interactions with iNOS protein

inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.112230openalex-snapshot

Phytotoxic neo-clerodane diterpenoids from the aerial parts of Scutellaria barbata

inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113771openalex-snapshot

Structure and anti-inflammatory activity of neo-clerodane diterpenoids from Scutellaria barbata

inferred← citeshttps://doi.org/10.1016/j.phytol.2016.10.020openalex-snapshot

Neoclerodane diterpenoids from aerial parts of Scutellaria barbata

inferred← citeshttps://doi.org/10.1016/j.phytol.2018.11.008openalex-snapshot

Scutebarbatolides A-C, new neo-clerodane diterpenoids from Scutellaria barbata D. Don with cytotoxic activity

inferred← citeshttps://doi.org/10.1016/j.phytol.2019.06.004openalex-snapshot

New acylated iridoid glucosides from Scutellaria glaphyrostachys Rech.f. and chemotaxonomic importance for the genus Scutellaria

inferred← citeshttps://doi.org/10.1016/j.tet.2016.10.034openalex-snapshot

Antiviral clerodane diterpenoids from Dodonaea viscosa

inferred← citeshttps://doi.org/10.1016/j.tet.2018.10.017openalex-snapshot

Vinyl nosylates as partner in copper and silver co-catalyzed Sonogashira cross-coupling reactions

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Advanced natural products chemistry research in China between 2015 and 2017

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00126openalex-snapshot

neo -Clerodane Diterpenoids from Scutellaria barbata and Their Inhibitory Effects on LPS-Induced Nitric Oxide Production

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00415openalex-snapshot

Semisynthesis of (−)-Rutamarin Derivatives and Their Inhibitory Activity on Epstein–Barr Virus Lytic Replication

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.6b03142openalex-snapshot

Euphomilones A and B, ent-Rosane Diterpenoids with 7/5/6 and 5/7/6 Skeletons from Euphorbia milii

inferred← citeshttps://doi.org/10.1039/c5ra22568jopenalex-snapshot

Discovering new DNA gyrase inhibitors using machine learning approaches

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FeCl 3 ·6H 2 O/acetaldehyde, a versatile system for the deprotection of ketals and acetals via a transacetalization process

inferred← citeshttps://doi.org/10.1039/c6np00059bopenalex-snapshot

Diterpenoids of terrestrial origin

inferred← citeshttps://doi.org/10.1039/c7ra08877aopenalex-snapshot

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

inferred← citeshttps://doi.org/10.1080/08927022.2019.1709638openalex-snapshot

Design and molecular docking studies of new inhibitor candidates for EBNA1 DNA binding site: a computational study

inferred← citeshttps://doi.org/10.1177/1934578x20933785openalex-snapshot

The NMR Spin Systems of Scutellaria 8β,13-Epoxy- neo -clerod-3-en-15,16-olides and Revision of 1 H and 13 C NMR Spectra Reported Data

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Therapeutic potential of rutamarin: preclinical evidence of its biological properties through in silico, in vitro, and in vivo studies

inferred← citeshttps://doi.org/10.2174/1381612825666191216124310openalex-snapshot

Scutellaria barbata: A Review on Chemical Constituents, Pharmacological Activities and Clinical Applications

inferred← citeshttps://doi.org/10.3389/fmicb.2026.1945077openalex-snapshot

Exploration of the mechanisms and active compounds of Scutellaria barbata D. Don against influenza A (H1N1) virus

inferred← citeshttps://doi.org/10.3389/fphar.2022.816029openalex-snapshot

Ethnobotanical Survey on Bitter Tea in Taiwan

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Comprehensive review of tujia “Lian” medicinal botanical drugs: traditional classification system, phytochemical, and pharmacological profile

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/molecules23112952openalex-snapshot

Transcriptomic Insight into Terpenoid Biosynthesis and Functional Characterization of Three Diterpene Synthases in Scutellaria barbata

inferred← citeshttps://doi.org/10.3390/molecules29174134openalex-snapshot

Chemical Constituents, Anti-Tumor Mechanisms, and Clinical Application: A Comprehensive Review on Scutellaria barbata

inferred← citeshttps://doi.org/10.3390/v13050826openalex-snapshot

Scutellaria barbata D. Don Inhibits the Main Proteases (Mpro and TMPRSS2) of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection

inferred← citeshttps://doi.org/10.3390/v16010124openalex-snapshot

Update of Natural Products and Their Derivatives Targeting Epstein–Barr Infection

inferred← citeshttps://doi.org/10.57634/rcr5056openalex-snapshot

Antiviral properties of diterpenes and their derivatives

inferred← citeshttps://doi.org/10.6023/cjoc202202016openalex-snapshot

Study on the Secondary Metabolites of the Endophytic Fungus Aspergillus terreus HQ100X-1 in Scutellaria formosana

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