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hERG Channel Inhibitory Daphnane Diterpenoid Orthoesters and Polycephalones A and B with Unprecedented Skeletons from Gnidia polycephala
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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/jat.1395openalex-snapshot
Collation, assessment and analysis of literature in vitro data on hERG receptor blocking potency for subsequent modeling of drugs' cardiotoxic properties
inferredcites →https://doi.org/10.1002/mrc.1260310208openalex-snapshot
NMR assignments and conformational analysis of yuanhuacin
inferredcites →https://doi.org/10.1007/s00424-006-0125-yopenalex-snapshot
Automated fast perfusion of Xenopus oocytes for drug screening
inferredcites →https://doi.org/10.1007/s00424-010-0868-3openalex-snapshot
Effects of lobeline, a nicotinic receptor ligand, on the cloned Kv1.5
inferredcites →https://doi.org/10.1016/j.bmc.2014.05.042openalex-snapshot
Topoisomerase II inhibitors from the roots of Stellera chamaejasme L.
inferredcites →https://doi.org/10.1016/j.pharmthera.2008.05.009openalex-snapshot
The hERG potassium channel and hERG screening for drug-induced torsades de pointes
inferredcites →https://doi.org/10.1016/j.phytochem.2014.05.008openalex-snapshot
Rare biscoumarin derivatives and flavonoids from Hypericum riparium
inferredcites →https://doi.org/10.1016/j.tetlet.2014.05.007openalex-snapshot
Daphnauranols A–C, new antifeedant sesquiterpenoids with a 5/6/7 ring system from Daphne aurantiaca
inferredcites →https://doi.org/10.1016/s0031-9422(03)00211-5openalex-snapshot
Phenylpropanoid glycosides of Gnidia polycephala
inferredcites →https://doi.org/10.1016/s0040-4039(00)72079-xopenalex-snapshot
Rearrangements of C11H10O ketones catalyzed by boron trifluoride
inferredcites →https://doi.org/10.1016/s0040-4039(01)96649-3openalex-snapshot
Structure and stereochemistry of huratoxin, a piscicidal constituent of
inferredcites →https://doi.org/10.1021/np200855dopenalex-snapshot
Library-Based Discovery and Characterization of Daphnane Diterpenes as Potent and Selective HIV Inhibitors in Daphne gnidium
inferredcites →https://doi.org/10.1021/np50037a018openalex-snapshot
Daphnane Diterpenes from Diarthron vesiculosum: Vesiculosin and Isovesiculosin
inferredcites →https://doi.org/10.1038/nature04710openalex-snapshot
hERG potassium channels and cardiac arrhythmia
inferredcites →https://doi.org/10.1038/sj.bjp.0707356openalex-snapshot
State dependent dissociation of HERG channel inhibitors
inferredcites →https://doi.org/10.1055/s-0030-1270920openalex-snapshot
hERG Channel Inhibitors in Extracts of Coptidis Rhizoma
inferredcites →https://doi.org/10.1055/s-0034-1368590openalex-snapshot
Natural Products as Potential Human Ether-A-Go-Go-Related Gene Channel Inhibitors – Screening of Plant-Derived Alkaloids
inferredcites →https://doi.org/10.1055/s-0034-1382900openalex-snapshot
Combined Use of Extract Libraries and HPLC-Based Activity Profiling for Lead Discovery: Potential, Challenges, and Practical Considerations
inferredcites →https://doi.org/10.1055/s-0034-1382907openalex-snapshot
Natural Products as Potential Human Ether-a-Go-Go-Related Gene Channel Inhibitors – Outcomes from a Screening of Widely Used Herbal Medicines and Edible Plants
inferredcites →https://doi.org/10.1080/00021369.1974.10861290openalex-snapshot
A Piscicidal Constituent ofExcoecaria agallocha
inferredcites →https://doi.org/10.1080/10286020701394431openalex-snapshot
Four new terpenoids from the roots of Ligularia narynensis
inferredcites →https://doi.org/10.1107/s0021889803021800openalex-snapshot
CRYSTALS version 12: software for guided crystal structure analysis
inferredcites →https://doi.org/10.1107/s0021889807029238openalex-snapshot
SUPERFLIP – a computer program for the solution of crystal structures by charge flipping in arbitrary dimensions
inferredcites →https://doi.org/10.1107/s0021889807067908openalex-snapshot
Mercury CSD 2.0 – new features for the visualization and investigation of crystal structures
inferredcites →https://doi.org/10.1107/s0108767393012784openalex-snapshot
The control of difficult refinements
inferredcites →https://doi.org/10.1111/j.1476-5381.2010.01159.xopenalex-snapshot
Trapping and dissociation of propafenone derivatives in HERG channels
inferredcites →https://doi.org/10.1136/heart.89.11.1363openalex-snapshot
Drug induced QT prolongation and torsades de pointes
inferredcites →https://doi.org/10.1161/01.cir.0000155617.54749.09openalex-snapshot
QTc Prolongation by Grapefruit Juice and Its Potential Pharmacological Basis
inferredcites →https://doi.org/10.1248/cpb.28.708openalex-snapshot
13C-nuclear magnetic resonance (NMR) spectral studies on polysubstituted flavonoids. I. 13C-NMR spectra of flavones.
inferredcites →https://doi.org/10.1248/cpb.48.964openalex-snapshot
Synthesis and Anti-platelet, Anti-inflammatory and Anti-allergic Activities of Methoxyisoflavanquinone and Related Compounds.
inferredcites →https://doi.org/10.1590/s0074-02761991000600049openalex-snapshot
Some progress on the chemistry of natural bioactive terpenoids form Chinese medicinal plants
inferredcites →https://doi.org/10.3987/com-98-8193openalex-snapshot
Regiospecific Demethylation-Sulfonation of 2',3'-Dimethoxyflavones
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.2020.112554zenodo-depositor-declared
Neuroprotective compounds from the resinous heartwood of Aquilaria sinensis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112628zenodo-depositor-declared
Guaiane-type sesquiterpenoids from the roots of Stellera chamaejasme L. and their neuroprotective activities
inferred← citeshttps://doi.org/10.1016/b978-0-443-40578-5.00002-7openalex-snapshot
Drug discovery from daphnane-type diterpenoids: a balance between the anti-HIV effect and toxicity
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106208openalex-snapshot
Guaiane-type sesquiterpenoids with various ring skeletons from Daphne bholua uncovered by molecular networking and structural revisions of previously reported analogues
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107208openalex-snapshot
New daphnane diterpenoidal 1,3,4-oxdiazole derivatives as potential anti-hepatoma agents: Synthesis, biological evaluation and molecular modeling studies
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.08.012openalex-snapshot
Chemical constituents from Daphne tangutica and their cytotoxicity against nasopharyngeal carcinoma cells
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.115540openalex-snapshot
Phytochemicals from Stellera chamaejasme alleviate psoriasis by modulating the immune microenvironment via the JAK2/PI3K/AKT pathway
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113523openalex-snapshot
Guide isolation of guaiane-type sesquiterpenoids from Daphne tangutica maxim. And their anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113950openalex-snapshot
Structurally diverse rearranged sesquiterpenoids, including a pair of rare tautomers, from the aerial parts of Daphne penicillata
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114376openalex-snapshot
Natural promising daphnane diterpenoids: An integrated review of their sources, structural classification, biological activities, and synthesis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.115018openalex-snapshot
Diterpenoids from the flower buds of Daphne genkwa induced the pyroptosis of HCT-116 cells by inhibiting STAT3 phosphorylation
inferred← citeshttps://doi.org/10.1016/j.trac.2019.01.002openalex-snapshot
Recent applications of high resolution mass spectrometry for the characterization of plant natural products
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00003openalex-snapshot
Daphnane Diterpenoids from Daphne genkwa Inhibit PI3K/Akt/mTOR Signaling and Induce Cell Cycle Arrest and Apoptosis in Human Colon Cancer Cells
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00527openalex-snapshot
Sesquiterpenoids from Seriphidium transiliense and Their Melanogenic Activity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00462openalex-snapshot
Aquilanols A and B, Macrocyclic Humulene-Type Sesquiterpenoids from the Agarwood of Aquilaria malaccensis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00690openalex-snapshot
Absolute Configurations and Bioactivities of Guaiane-Type Sesquiterpenoids Isolated fromPogostemon cablin
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00500openalex-snapshot
Diterpenoids from Euphorbia dulcis with Potassium Ion Channel Inhibitory Activity with Selective G Protein-Activated Inwardly Rectifying Ion Channel (GIRK) Blocking Effect
inferred← citeshttps://doi.org/10.1039/c6np00059bopenalex-snapshot
Diterpenoids of terrestrial origin
inferred← citeshttps://doi.org/10.1039/c7np00014fopenalex-snapshot
Natural products modulating the hERG channel: heartaches and hope
inferred← citeshttps://doi.org/10.1080/14786419.2022.2062349openalex-snapshot
A new gnidiflavanone-flavonol dimer and other constituents from Gnidia apiculata
inferred← citeshttps://doi.org/10.1177/1934578x1701201103openalex-snapshot
New Primula -type Flavones from Exudates of Selected Dionysia spp. (Primulaceae)
inferred← citeshttps://doi.org/10.3390/v14071437openalex-snapshot
HPLC-Based Purification and Isolation of Potent Anti-HIV and Latency Reversing Daphnane Diterpenes from the Medicinal Plant Gnidia sericocephala (Thymelaeaceae)
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