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Neolignans and Sesquiterpenoid from Piper yunnanense
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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/cbdv.201300208openalex-snapshot
Three New Phenylpropanoids from the Roots of Piper taiwanense and Their Inhibitory Activities on Platelet Aggregation and Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1002/cbdv.201600133openalex-snapshot
Chemodiversity Associated with Cytotoxicity and Antimicrobial Activity ofPiper aduncumvar.ossanum
inferredcites →https://doi.org/10.1002/cbdv.202000144openalex-snapshot
MsrA Efflux Pump Inhibitory Activity of Piper cubeba L.f. and its Phytoconstituents against Staphylococcus aureus RN4220
inferredcites →https://doi.org/10.1002/cbdv.202000245openalex-snapshot
Analysis of Chemical Composition and Assessment of Antioxidant, Cytotoxic and Synergistic Antibacterial Activities of Essential Oils from Different Plant Parts of Piper boehmeriifolium
inferredcites →https://doi.org/10.1016/j.bioorg.2019.103099openalex-snapshot
(±)-Meliviticines A and B: Rearranged prenylated acetophenone derivatives from Melicope viticina and their antimicrobial activity
inferredcites →https://doi.org/10.1016/j.bmcl.2020.127682openalex-snapshot
A new sesquineolignan and four new neolignans isolated from the leaves of Piper betle, a traditional medicinal plant in Myanmar
inferredcites →https://doi.org/10.1016/j.fitote.2020.104544openalex-snapshot
Four new chemical constituents from Piper pleiocarpum
inferredcites →https://doi.org/10.1021/acs.jafc.0c02885openalex-snapshot
Lignans and Neolignans with Antioxidant and Human Cancer Cell Proliferation Inhibitory Activities from Cinnamomum bejolghota Confirm Its Functional Food Property
inferredcites →https://doi.org/10.1021/acs.jafc.8b05359openalex-snapshot
Development of a Validated High-Performance Liquid Chromatography Method and Optimization of the Extraction of Lignans fromPiper cubeba
inferredcites →https://doi.org/10.1021/acs.jafc.9b01320openalex-snapshot
Alkaloids from Piper nigrum Synergistically Enhanced the Effect of Paclitaxel against Paclitaxel-Resistant Cervical Cancer Cells through the Downregulation of Mcl-1
inferredcites →https://doi.org/10.1021/acs.jafc.9b07754openalex-snapshot
Alkaloids from Black Pepper (Piper nigrum L.) Exhibit Anti-Inflammatory Activity in Murine Macrophages by Inhibiting Activation of NF-κB Pathway
inferredcites →https://doi.org/10.1021/acs.jnatprod.1c00055openalex-snapshot
New Tyramine- and Aporphine-Type Alkamides with NO Release Inhibitory Activities from Piper puberulum
inferredcites →https://doi.org/10.1021/acs.jnatprod.8b00589openalex-snapshot
Prenylated Indole Diterpene Alkaloids from a Mine-Soil-Derived Tolypocladium sp.
inferredcites →https://doi.org/10.1021/acs.joc.0c02682openalex-snapshot
Neolignans from Piper betle Have Synergistic Activity against Antibiotic-Resistant Staphylococcus aureus
inferredcites →https://doi.org/10.1021/acs.joc.1c00240openalex-snapshot
Piperhancins A and B, Two Pairs of Antineuroinflammatory Cycloneolignane Enantiomers from Piper hancei
inferredcites →https://doi.org/10.1021/jp992097lopenalex-snapshot
A Smooth Solvation Potential Based on the Conductor-Like Screening Model
inferredcites →https://doi.org/10.1021/np100004vopenalex-snapshot
AC-Glycosylflavone fromPiper ossanum, a Compound Conformationally Controlled by CH/π and Other Weak Intramolecular Interactions
inferredcites →https://doi.org/10.1021/np100606uopenalex-snapshot
Cytotoxic Amide Alkaloids from Piper boehmeriaefolium
inferredcites →https://doi.org/10.1021/np200557eopenalex-snapshot
Bioassay-Guided Isolation of Constituents of Piper sarmentosum Using a Mitochondrial Transmembrane Potential Assay
inferredcites →https://doi.org/10.1021/np300703uopenalex-snapshot
Nudibaccatumone, a Trimer Comprising a Phenylpropanoid and Two Sesquiterpene Moieties from Piper nudibaccatum
inferredcites →https://doi.org/10.1021/np300911bopenalex-snapshot
Evaluation of Constituents of Piper retrofractum Fruits on Neurotrophic Activity
inferredcites →https://doi.org/10.1021/np400886sopenalex-snapshot
Antiherbivore Prenylated Benzoic Acid Derivatives from Piper kelleyi
inferredcites →https://doi.org/10.1021/np800104popenalex-snapshot
Benzoic Acid Derivatives from Piper Species and Their Antiparasitic Activity
inferredcites →https://doi.org/10.1080/14786419.2018.1495634openalex-snapshot
The new ether derivative of phenylpropanoid and bioactivity was investigated from the leaves of Piper betle L.
inferredcites →https://doi.org/10.1080/14786419.2018.1539982openalex-snapshot
N-Alkylamides from Piper longum L. and their stimulative effects on the melanin content and tyrosinase activity in B16 melanoma cells
inferredcites →https://doi.org/10.1080/14786419.2019.1593167openalex-snapshot
Pleiocarpumlignan A, a new dineolignan from Piper pleiocarpum Chang ex Tseng
inferredcites →https://doi.org/10.1103/physreva.38.3098openalex-snapshot
Density-functional exchange-energy approximation with correct asymptotic behavior
inferredcites →https://doi.org/10.3390/molecules24071364openalex-snapshot
Piper Species: A Comprehensive Review on Their Phytochemistry, Biological Activities and Applications
inferredcites →https://doi.org/10.60692/m8f95-jtj33openalex-snapshot
N-Alkylamides from Piper longum L. and their stimulative effects on the melanin content and tyrosinase activity in B16 melanoma 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.2022.113326zenodo-depositor-declared
Review of lignans from 2019 to 2021: Newly reported compounds, diverse activities, structure-activity relationships and clinical applications
inferred← citeshttps://doi.org/10.1002/ecy.3765openalex-snapshot
Testing the role of local plant chemical diversity on plant–herbivore interactions and plant species coexistence
inferred← citeshttps://doi.org/10.1007/s10600-026-05056-3openalex-snapshot
Phytochemical Constituents from Piper yunnanense with Anti-Inflammatory Activity
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105403openalex-snapshot
Lignans from the genus Piper L. and their pharmacological activities: An updated review
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.139070openalex-snapshot
Structural elucidation of two new ursane-type triterpenoids from Syzygium handelii by spectroscopic analyses and calculations
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114409openalex-snapshot
Artemyriantholidimers A-G, undescribed guaiane-type sesquiterpenoid dimers from Artemisia myriantha and their antihepatoma activities
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