On the public citation graph
Medicinal Attributes of Lignans Extracted from Piper Cubeba: Current Developments
0 signed · 87 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archinte.1997.00440400063008openalex-snapshot
Stress Management and Exercise Training in Cardiac Patients With Myocardial Ischemia
inferredcites →https://doi.org/10.1002/ardp.19873200416openalex-snapshot
Orientierung der Hydroxyl‐Gruppe des (−)‐Cubebins und seines Epimeren Orientation of the Hydroxyl Group of (−)‐Cubebin and its Epimer
inferredcites →https://doi.org/10.1002/open.201700182openalex-snapshot
Medicinal Attributes of Lignans Extracted from Piper Cubeba: Current Developments
inferredcites →https://doi.org/10.1002/ptr.4932openalex-snapshot
The Lignan (‐)‐Cubebin Inhibits Vascular Contraction and Induces Relaxation Via Nitric Oxide Activation in Isolated Rat Aorta
inferredcites →https://doi.org/10.1007/bf01623898openalex-snapshot
Antioxidant activity of secoisolariciresinol diglucoside-derived metabolites, secoisolariciresinol, Enterodiol, and enterolactone
inferredcites →https://doi.org/10.1007/s00436-010-1725-1openalex-snapshot
(−)−Hinokinin-loaded poly(d,l-lactide-co-glycolide) microparticles for Chagas disease
inferredcites →https://doi.org/10.1007/s00436-010-1885-zopenalex-snapshot
Reduction of parasitism tissue by treatment of mice chronically infected with Trypanosoma cruzi with lignano lactones
inferredcites →https://doi.org/10.1007/s10086-007-0892-xopenalex-snapshot
Biosynthesis of lignans and norlignans
inferredcites →https://doi.org/10.1007/s13659-015-0073-3openalex-snapshot
Total Synthesis of Lignan Lactone (–)-Hinokinin
inferredcites →https://doi.org/10.1016/0031-9422(88)80219-xopenalex-snapshot
Lignans of Piper trichostachyon
inferredcites →https://doi.org/10.1016/0040-4039(88)85304-8openalex-snapshot
Total synthesis of the lignans (-)- and (+)-burseran, (-)-cubebin, and (-)-hinokinin by diastereoselective conjugate addition of benzyl anions to 2-(R) and (s)-benzyloxy-2,5-dihydro-4-(3,4-methylenedioxybenzoyzfuran
inferredcites →https://doi.org/10.1016/j.bjp.2015.12.006openalex-snapshot
Antibacterial activity of (−)-cubebin isolated from Piper cubeba and its semisynthetic derivatives against microorganisms that cause endodontic infections
inferredcites →https://doi.org/10.1016/j.bmcl.2004.10.079openalex-snapshot
Trypanocidal activity of (−)-cubebin derivatives against free amastigote forms of Trypanosoma cruzi
inferredcites →https://doi.org/10.1016/j.bmcl.2004.12.035openalex-snapshot
Synthesis and biological activity evaluation of lignan lactones derived from (−)-cubebin
inferredcites →https://doi.org/10.1016/j.bmcl.2016.02.041openalex-snapshot
Anticancer activity studies of cubebin isolated from Piper cubeba and its synthetic derivatives
inferredcites →https://doi.org/10.1016/j.bmcl.2016.11.081openalex-snapshot
In vivo and in silico anti-inflammatory mechanism of action of the semisynthetic (−)-cubebin derivatives (−)-hinokinin and (−)-O-benzylcubebin
inferredcites →https://doi.org/10.1016/j.bse.2007.01.003openalex-snapshot
Lignan profile of Piper cubeba, an Indonesian medicinal plant
inferredcites →https://doi.org/10.1016/j.catcom.2008.11.013openalex-snapshot
Synthesis of (−)-hinokinin by oxidation of (−)-cubebin catalyzed by biomimetic metalloporphyrin catalytic systems
inferredcites →https://doi.org/10.1016/j.exppara.2012.12.005openalex-snapshot
Evaluation of the in vivo therapeutic properties of (−)-cubebin and (−)-hinokinin against Trypanosoma cruzi
inferredcites →https://doi.org/10.1016/j.fct.2006.10.012openalex-snapshot
(−)-Hinokinin causes antigenotoxicity but not genotoxicity in peripheral blood of Wistar rats
inferredcites →https://doi.org/10.1016/j.fct.2010.05.056openalex-snapshot
Lignans inhibit cell growth via regulation of Wnt/β-catenin signaling
inferredcites →https://doi.org/10.1016/j.fct.2013.01.050openalex-snapshot
A comparative study of the modulatory effects of (−)-cubebin on the mutagenicity/recombinogenicity induced by different chemical agents
inferredcites →https://doi.org/10.1016/j.jpha.2014.03.001openalex-snapshot
Quantitative estimation of (-)-hinokinin, a trypanosomicidal marker in Piper cubeba, and some of its commercial formulations using HPLC-PDA
inferredcites →https://doi.org/10.1016/j.mrgentox.2010.04.023openalex-snapshot
Effect of the dibenzylbutyrolactone lignan (−)-hinokinin on doxorubicin and methyl methanesulfonate clastogenicity in V79 Chinese hamster lung fibroblasts
inferredcites →https://doi.org/10.1016/j.phcgj.2012.12.001openalex-snapshot
Anti-inflammatory and analgesic evaluation of hydroalcoholic extract and fractions from seeds of Piper cubeba L. (Piperaceae)
inferredcites →https://doi.org/10.1016/j.phytochem.2006.01.019openalex-snapshot
Configurational analysis of cubebins and bicubebin from Aristolochia lagesiana and Aristolochia pubescens
inferredcites →https://doi.org/10.1016/j.tifs.2016.06.007openalex-snapshot
Biological effects induced by estrogenic activity of lignans
inferredcites →https://doi.org/10.1016/s0031-9422(00)81752-5openalex-snapshot
Lignans of Piper cubeba☆
inferredcites →https://doi.org/10.1016/s0031-9422(00)83546-3openalex-snapshot
Lignans from Piper cubeba
inferredcites →https://doi.org/10.1016/s0031-9422(00)84055-8openalex-snapshot
Dibenzylbutyrolactone lignans from Virola sebifera
inferredcites →https://doi.org/10.1016/s0031-9422(97)00199-4openalex-snapshot
Lignoids, flavanoids and polyketides of Virola surinamensis
inferredcites →https://doi.org/10.1016/s0378-8741(01)00171-4openalex-snapshot
Anti-inflammatory activity of cubebin, a lignan from the leaves of Zanthoxyllum naranjillo Griseb
inferredcites →https://doi.org/10.1016/s0378-8741(03)00280-0openalex-snapshot
Investigations of anti-inflammatory and antinociceptive activities of Piper cubeba, Physalis angulata and Rosa hybrida
inferredcites →https://doi.org/10.1017/s0007114509992753openalex-snapshot
Health effects with consumption of the flax lignan secoisolariciresinol diglucoside
inferredcites →https://doi.org/10.1021/acs.orglett.7b02644openalex-snapshot
Total Synthesis of (−)-Bicubebin A, B, (+)-Bicubebin C and Structural Reassignment of (−)-cis-Cubebin
inferredcites →https://doi.org/10.1021/jf0629134openalex-snapshot
Quantification of a Broad Spectrum of Lignans in Cereals, Oilseeds, and Nuts
inferredcites →https://doi.org/10.1021/np400452nopenalex-snapshot
The Lignan (−)-Hinokinin Displays Modulatory Effects on Human Monoamine and GABA Transporter Activities
inferredcites →https://doi.org/10.1038/298659a0openalex-snapshot
Origin of lignans in mammals and identification of a precursor from plants
inferredcites →https://doi.org/10.1039/c6np00021eopenalex-snapshot
Recent advances in research on lignans and neolignans
inferredcites →https://doi.org/10.1039/j39690002470openalex-snapshot
Chemistry and synthesis of the lignan (–)-cubebin
inferredcites →https://doi.org/10.1039/p19880001603openalex-snapshot
Synthesis of lignans related to the podophyllotoxin series
inferredcites →https://doi.org/10.1039/p19880001615openalex-snapshot
A short versatile synthesis of aryltetralin lignans including deoxyisopodophyllotoxin and epi-isopodophyllotoxin
inferredcites →https://doi.org/10.1055/s-0042-101761openalex-snapshot
(−)-Hinokinin Induces G2/M Arrest and Contributes to the Antiproliferative Effects of Doxorubicin in Breast Cancer Cells
inferredcites →https://doi.org/10.1080/14786419.2014.905563openalex-snapshot
Isolation, structural elucidation and anti-inflammatory activity of astragalin, ( − )hinokinin, aristolactam I and aristolochic acids (I & II) fromAristolochia indica
inferredcites →https://doi.org/10.1080/14786419.2017.1380017openalex-snapshot
Biotransformation of (-)-cubebin byAspergillusspp. into (-)-hinokinin and (-)-parabenzlactone, and their evaluation against oral pathogenic bacteria
inferredcites →https://doi.org/10.1080/15287394.2015.1110067openalex-snapshot
Evaluation of lignan (–)-cubebin extracted fromPiper cubebaon human colon adenocarcinoma cells (HT29)
inferredcites →https://doi.org/10.1093/carcin/bgm255openalex-snapshot
Chemopreventive properties of pinoresinol-rich olive oil involve a selective activation of the ATM–p53 cascade in colon cancer cell lines
inferredcites →https://doi.org/10.1093/jn/135.5.1056openalex-snapshot
Dietary Sesamin Is Converted to Enterolactone in Humans
inferredcites →https://doi.org/10.1111/j.1365-2672.1985.tb01427.xopenalex-snapshot
Production and metabolism of lignans by the human faecal flora
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03558.xopenalex-snapshot
Hinokinin biosynthesis in Linum corymbulosum Reichenb.
inferredcites →https://doi.org/10.1155/2012/593403openalex-snapshot
Antiprotozoal and Antimycobacterial Activities of Pure Compounds fromAristolochia elegansRhizomes
inferredcites →https://doi.org/10.1158/1535-7163.mct-07-0220openalex-snapshot
Enterolactone induces apoptosis in human prostate carcinoma LNCaP cells via a mitochondrial-mediated, caspase-dependent pathway
inferredcites →https://doi.org/10.1158/1541-7786.mcr-09-0565openalex-snapshot
Sesamin Manifests Chemopreventive Effects through the Suppression of NF-κB–Regulated Cell Survival, Proliferation, Invasion, and Angiogenic Gene Products
inferredcites →https://doi.org/10.1159/000443655openalex-snapshot
Heilpflanze des Jahres 2016: Kubeben-Pfeffer (Piper cubeba)
inferredcites →https://doi.org/10.1177/1557988306298623openalex-snapshot
Treatment of Erectile Dysfunction: Update
inferredcites →https://doi.org/10.1186/1472-6882-12-203openalex-snapshot
Mutagenicity and antimutagenicity of (−)-hinokinin a trypanosomicidal compound measured by Salmonella microsome and comet assays
inferredcites →https://doi.org/10.1515/znb-2007-0117openalex-snapshot
Asymmetric Synthesis of (+)-Hinokinin, (+)-Dihydrocubebin and Cubebin Dimethyl Ether, a New Lignan from Phyllanthus niruri
inferredcites →https://doi.org/10.1515/znc-2009-11-1204openalex-snapshot
Antimycobacterial Activity of Natural and Semi-Synthetic Lignans
inferredcites →https://doi.org/10.1590/1983-084x/14_085openalex-snapshot
Avaliação da atividade antimicobacteriana da lignana diidrocubebina extraída da Piper cubeba e de seus derivados semissintéticos
inferredcites →https://doi.org/10.21577/1984-6835.20170039openalex-snapshot
Cubebin: A Small Molecule with Great Potential
inferredcites →https://doi.org/10.3390/molecules190914862openalex-snapshot
Hinokinin, an Emerging Bioactive Lignan
inferredcites →https://doi.org/10.3390/nu7042707openalex-snapshot
Cytotoxic Activity of Piper cubeba Extract in Breast Cancer Cell Lines
inferredcites →https://doi.org/10.4103/2225-4110.124811openalex-snapshot
Anticancer Principles from Medicinal Piper (胡椒 Hú Jiāo) Plants
inferredcites →https://doi.org/10.4103/2229-5119.110340openalex-snapshot
Phytoconstituents responsible for anti-inflammatory activity
inferredcites →https://doi.org/10.5897/ajpp2015.4490openalex-snapshot
Cubebin and semisynthetic dibenzyl butyrolactone derivatives: Biological activities
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/pharmacia.72.e144711zenodo-depositor-declared
The potential of kemukus (Piper cubeba L.f.) seed essential oil nanoemulsion on behavior and biochemical parameters in a rat model of scopolamine-induced Alzheimer’s disease
inferred← citeshttps://doi.org/10.1002/cbdv.202401065openalex-snapshot
Inhibitory Activity of Compounds Isolated from Ligustrum robustum (Roxb.) Against HepG2 Liver Cancer Cells: Isocubein and 4‐(2‐Acetoxyethyl)phenol as Potential Candidates
inferred← citeshttps://doi.org/10.1007/s00203-021-02417-0openalex-snapshot
Optimization of (–)-cubebin biotransformation to (–)-hinokinin by the marine fungus Absidia coerulea 3A9
inferred← citeshttps://doi.org/10.1016/b978-0-443-30170-4.00011-5openalex-snapshot
Chemistry and pharmacology of lignans and stilbenes reported in African medicinal plants
inferred← citeshttps://doi.org/10.1016/j.jgeb.2026.100724openalex-snapshot
Investigating the prognostics and theranostic cell cycle-related genes of Hinokinin in high-grade glioma: an integrated network pharmacology, bioinformatics, and molecular docking approach
inferred← citeshttps://doi.org/10.1016/j.jphs.2021.09.002openalex-snapshot
Effect of Piper cubeba total extract and isolated lignans on head and neck cancer cell lines and normal fibroblasts
inferred← citeshttps://doi.org/10.1016/j.vetpar.2019.108932openalex-snapshot
In vitro anthelmintic activity of the crude hydroalcoholic extract of Piper cubeba fruits and isolated natural products against gastrointestinal nematodes in sheep
inferred← citeshttps://doi.org/10.1016/j.vetpar.2023.110001openalex-snapshot
Molecular interaction analysis of the lignans from Piper cubeba in complex with Haemonchus contortus phosphomethyltransferase
inferred← citeshttps://doi.org/10.1016/j.vetpar.2024.110348openalex-snapshot
In vivo anthelmintic activity of hydroethanolic extract of Piper cubeba fruits in sheep naturally infected with gastrointestinal nematodes
inferred← citeshttps://doi.org/10.1080/14786419.2022.2131784openalex-snapshot
Larvicidal potential of extracts and isolated compounds from Piper cubeba fruits against Aedes aegypti (Diptera: Culicidae) larvae
inferred← citeshttps://doi.org/10.1080/14786419.2023.2177849openalex-snapshot
A review on multi-therapeutic potential of (-)-cubebin: experimental evidences
inferred← citeshttps://doi.org/10.13005/bpj/2908openalex-snapshot
Computational Investigation of Bioactive Phytoconstituents as SarS-Cov-2 Main Protease Inhibitors Through Molecular Docking and Interaction Fingerprint Studies
inferred← citeshttps://doi.org/10.1515/tjb-2023-0032openalex-snapshot
Neuroprotective effects of Cubebin and Hinokinin lignan fractions of Piper cubeba fruit in Alzheimer’s disease in vitro model
inferred← citeshttps://doi.org/10.1590/1519-6984.266573openalex-snapshot
Neuroprotective potential of lignan-rich fraction of Piper cubeba L. by improving antioxidant capacity in the rat's brain
inferred← citeshttps://doi.org/10.18311/jnr/2024/43896openalex-snapshot
Stability Indicating HPTLC Method for Estimation of Cubebin in Crude Drug and Marketed Formulations
inferred← citeshttps://doi.org/10.2174/0113862073316439240515072946openalex-snapshot
Lignans: Advances in Biosynthesis, Bioavailability, and Pharmacological Activity
inferred← citeshttps://doi.org/10.3389/fphar.2021.685116openalex-snapshot
Plant-Derived Compounds as Promising Therapeutics for Vitiligo
inferred← citeshttps://doi.org/10.4103/pm.pm_288_19openalex-snapshot
Anticancer effects of piperine-free Piper nigrum extract on cholangiocarcinoma cell lines
inferred← citeshttps://doi.org/10.4314/bcse.v33i3.19openalex-snapshot
Chemical constituents and lipoxygenase inhibitory activity of Piper stylosum Miq.
inferred← citeshttps://doi.org/10.47749/t/unicamp.2019.1157151openalex-snapshot
Estudo comparativo de métodos de extração e cromatográficos para a obtenção da cubebina e da hinoquinina a partir das sementes de Piper cubeba L.
showing the first 20 of 21 · page through all 21
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.