On the public citation graph
Pteryxin - A promising butyrylcholinesterase-inhibiting coumarin derivative from Mutellina purpurea
0 signed · 78 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known work and none has been retracted — and get a dated CiteStamped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/10.1007/bf02906767openalex-snapshot
Extractive studies of the roots of Pteryxia terebinthina var. terebinthina and the isolation of Pteryxin
inferredcites →https://doi.org/10.1016/0006-2952(61)90145-9openalex-snapshot
A new and rapid colorimetric determination of acetylcholinesterase activity
inferredcites →https://doi.org/10.1016/j.bioorg.2015.08.002openalex-snapshot
Synthesis, molecular docking, acetylcholinesterase and butyrylcholinesterase inhibitory potential of thiazole analogs as new inhibitors for Alzheimer disease
inferredcites →https://doi.org/10.1016/j.bmc.2005.08.038openalex-snapshot
Inhibitory effects of coumarin and acetylene constituents from the roots of Angelica furcijuga on d-galactosamine/lipopolysaccharide-induced liver injury in mice and on nitric oxide production in lipopolysaccharide-activated mouse peritoneal macrophages
inferredcites →https://doi.org/10.1016/j.cbi.2016.05.001openalex-snapshot
Coumarins as cholinesterase inhibitors: A review
inferredcites →https://doi.org/10.1016/j.ejmech.2014.05.056openalex-snapshot
Synthesis and anti-cholinesterase activity of new 7-hydroxycoumarin derivatives
inferredcites →https://doi.org/10.1016/j.foodchem.2013.12.026openalex-snapshot
Quantitative analysis of phenolic metabolites from different parts of Angelica keiskei by HPLC–ESI MS/MS and their xanthine oxidase inhibition
inferredcites →https://doi.org/10.1016/j.jep.2013.12.053openalex-snapshot
The treatment of Alzheimer's disease using Chinese Medicinal Plants: From disease models to potential clinical applications
inferredcites →https://doi.org/10.1016/j.jff.2016.11.030openalex-snapshot
In vivo and in vitro anti-obesity activities of dihydropyranocoumarins derivatives from Peucedanum japonicum Thunb
inferredcites →https://doi.org/10.1016/j.nut.2014.01.015openalex-snapshot
Pteryxin: A coumarin in Peucedanum japonicum Thunb leaves exerts antiobesity activity through modulation of adipogenic gene network
inferredcites →https://doi.org/10.1016/j.phytol.2011.08.016openalex-snapshot
An in vitro and in silico approach to cholinesterase inhibitory and antioxidant effects of the methanol extract, furanocoumarin fraction, and major coumarins of Angelica officinalis L. fruits
inferredcites →https://doi.org/10.1021/jm300871xopenalex-snapshot
Structures of Human Acetylcholinesterase in Complex with Pharmacologically Important Ligands
inferredcites →https://doi.org/10.1021/jm501195eopenalex-snapshot
Discovery, Biological Evaluation, and Crystal Structure of a Novel Nanomolar Selective Butyrylcholinesterase Inhibitor
inferredcites →https://doi.org/10.1021/np000441wopenalex-snapshot
Coumarins Isolated from Angelica gigas Inhibit Acetylcholinesterase: Structure−Activity Relationships
inferredcites →https://doi.org/10.1055/s-0042-108738openalex-snapshot
Efficient Isolation of Dihydropyranocoumarins and Simple Coumarins from Mutellina purpurea Fruits
inferredcites →https://doi.org/10.1073/pnas.0508575102openalex-snapshot
Selective butyrylcholinesterase inhibition elevates brain acetylcholine, augments learning and lowers Alzheimer β-amyloid peptide in rodent
inferredcites →https://doi.org/10.1074/jbc.m210241200openalex-snapshot
Crystal Structure of Human Butyrylcholinesterase and of Its Complexes with Substrate and Products
inferredcites →https://doi.org/10.1111/j.1600-0773.1983.tb01095.xopenalex-snapshot
Coronary Vasodilatory, Spasmolytic and cAMP‐Phosphodiesterase Inhibitory Properties of Dihydropyranocoumarins and Dihydrofuranocoumarins
inferredcites →https://doi.org/10.1248/cpb.48.1429openalex-snapshot
Medicinal Foodstuffs. XX. Vasorelaxant Active Constituents from the Roots of Angelica furcijuga KITAGAWA: Structures of Hyuganins A, B, C, and D.
inferredcites →https://doi.org/10.1515/znc-2008-5-610openalex-snapshot
Coumarin, Anthroquinone and Stilbene Derivatives with Anticholinesterase Activity
inferredcites →https://doi.org/10.1586/ern.12.43openalex-snapshot
New and emerging treatments for Alzheimer’s disease
inferredcites →https://doi.org/10.2174/138955711796575434openalex-snapshot
An Overview on Natural Cholinesterase Inhibitors - A Multi-Targeted Drug Class - and Their Mass Production
inferredcites →https://doi.org/10.2174/15680266113139990142openalex-snapshot
Natural Products as Sources of New Lead Compounds for the Treatment of Alzheimer’s Disease
inferredcites →https://doi.org/10.2174/1568026615666150427113103openalex-snapshot
Coumarins: Auspicious Cholinesterase and Monoamine Oxidase Inhibitors
inferredcites →https://doi.org/10.2174/1568026615666150610143510openalex-snapshot
Computer Aided Drug Design Studies in the Discovery of Secondary Metabolites Targeted Against Age-Related Neurodegenerative Diseases
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4633265openalex-extracted
Carltonine-Derived Compounds for Targeted Butyrylcholinesterase Inhibition
inferred← citeshttps://doi.org/10.1002/9780470027318.a9925.pub2openalex-snapshot
Coumarins: Analytical and Preparative Techniques
inferred← citeshttps://doi.org/10.1002/9781119794127.ch3openalex-snapshot
Drug Discovery from Medicinal Plants against Alzheimer's Disease
inferred← citeshttps://doi.org/10.1002/ardp.201800247openalex-snapshot
Synthesis, CYP 450 evaluation, and docking simulation of novel 4‐aminopyridine and coumarin derivatives
inferred← citeshttps://doi.org/10.1002/cbdv.201800662openalex-snapshot
Clinanthus microstephium, an Amaryllidaceae Species with Cholinesterase Inhibitor Alkaloids: Structure−Activity Analysis of Haemanthamine Skeleton Derivatives
inferred← citeshttps://doi.org/10.1002/cbdv.201900017openalex-snapshot
Profiling Auspicious Butyrylcholinesterase Inhibitory Activity of Two Herbal Molecules: Hyperforin and Hyuganin C
inferred← citeshttps://doi.org/10.1002/cbdv.201900333openalex-snapshot
Metabolite Profiling by Hyphenated Liquid Chromatographic Mass Spectrometric Technique (HPLC‐DAD‐ESI‐Q‐TOF‐MS/MS) and Neurobiological Potential of Haplophyllum sahinii and H. vulcanicum Extracts
inferred← citeshttps://doi.org/10.1002/cbdv.202200315openalex-snapshot
Evaluation of Anti‐Alzheimer Activity of Synthetic Coumarins by Combination of in Vitro and in Silico Approaches
inferred← citeshttps://doi.org/10.1002/slct.201803672openalex-snapshot
Phyto‐Tacrine Hybrids as Promising Drugs to Treat Alzheimer's Disease
inferred← citeshttps://doi.org/10.1007/978-3-030-04624-8_26openalex-snapshot
Nutraceuticals for Cognitive Dysfunction
inferred← citeshttps://doi.org/10.1007/s10876-021-02099-0openalex-snapshot
Bioactive Molecules Coated Silver Oxide Nanoparticle Synthesis from Curcuma zanthorrhiza and HR-LCMS Monitored Validation of Its Photocatalytic Potency Towards Malachite Green Degradation
inferred← citeshttps://doi.org/10.1016/b978-0-12-813374-3.00014-4openalex-snapshot
Therapeutic Evaluation of Herbs With Enzyme Inhibition Studies
inferred← citeshttps://doi.org/10.1016/b978-0-12-817901-7.00009-5openalex-snapshot
Neuroprotective potential of phytochemicals via in silico molecular docking techniques
inferred← citeshttps://doi.org/10.1016/b978-0-443-15650-2.00003-9openalex-snapshot
In the design and development of neurotherapeutics agents
inferred← citeshttps://doi.org/10.1016/b978-0-443-23763-8.00034-8openalex-snapshot
Neuroprotection induced by coumarins in central nervous system disease models
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.111609openalex-snapshot
Potential therapeutic natural products against Alzheimer's disease with Reference of Acetylcholinesterase
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.114898openalex-snapshot
Pteryxin suppresses osteoclastogenesis and prevents bone loss via inhibiting the MAPK/Ca2+ signaling pathways mediated by ROS
inferred← citeshttps://doi.org/10.1016/j.bjp.2019.08.001openalex-snapshot
Selective BuChE inhibitory activity, chemical composition, and enantiomer content of the volatile oil from the Ecuadorian plant Clinopodium brownei
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.117401openalex-snapshot
Phytomolecules as Alzheimer's therapeutics: A comprehensive review
inferred← citeshttps://doi.org/10.1016/j.fct.2017.08.003openalex-snapshot
IXth International Symposium on Natural Products Chemistry and its Applications (IX-ISNPCA), Termas de Chillan, Chillan, Chile
inferred← citeshttps://doi.org/10.1016/j.foodchem.2018.08.044openalex-snapshot
Report on the 2nd International Symposium on Phytochemicals in Medicine and Food (4–7 April 2017, FuZhou, China)
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2018.09.014openalex-snapshot
Cholinesterases inhibition studies of biological active compounds from the rhizomes of Alpinia officinarum Hance and in silico molecular dynamics
inferred← citeshttps://doi.org/10.1016/j.jep.2021.114753openalex-snapshot
Pteryxin attenuates LPS-induced inflammatory responses and inhibits NLRP3 inflammasome activation in RAW264.7 cells
inferred← citeshttps://doi.org/10.1016/j.jep.2021.114924openalex-snapshot
Protective effect of pteryxin on LPS-induced acute lung injury via modulating MAPK/NF-κB pathway and NLRP3 inflammasome activation
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.132799openalex-snapshot
In vitro studies of a series of synthetic compounds for their anti-acetylcholinesterase activities identified arylpyrano[2,3-f]coumarins as hit compounds
inferred← citeshttps://doi.org/10.1016/j.phymed.2018.10.030openalex-snapshot
High-performance counter-current chromatography isolation and initial neuroactivity characterization of furanocoumarin derivatives from Peucedanum alsaticum L (Apiaceae)
inferred← citeshttps://doi.org/10.1016/j.phytol.2021.05.001openalex-snapshot
Butyrylcholinesterase-inhibiting natural coumarin molecules as potential leads
inferred← citeshttps://doi.org/10.1016/j.prmcm.2024.100405openalex-snapshot
Biological potential and therapeutic effectiveness of pteryxin in medicine. A viable alternative to current remedies for the treatment of human disorders
inferred← citeshttps://doi.org/10.1016/j.sajb.2019.01.020openalex-snapshot
Antioxidant and anticholinesterase potential of Ferulago cassia with farther bio-guided isolation of active coumarin constituents
inferred← citeshttps://doi.org/10.1038/s41598-020-78782-5openalex-snapshot
Acetylcholinesterase and butyrylcholinesterase inhibitory activities of khellactone coumarin derivatives isolated from Peucedanum japonicum Thurnberg
inferred← citeshttps://doi.org/10.1039/d4md00060aopenalex-snapshot
Carltonine-derived compounds for targeted butyrylcholinesterase inhibition
inferred← citeshttps://doi.org/10.1039/d6ra01662fopenalex-snapshot
Design, synthesis, and evaluation of pyrano[3,2- c ]coumarin derivatives for simultaneous targeting of amyloid-β 42 and acetylcholinesterase in transgenic AD model of Drosophila
inferred← citeshttps://doi.org/10.1080/14756366.2018.1491847openalex-snapshot
The insight of in vitro and in silico studies on cholinesterase inhibitors from the roots of Cimicifuga dahurica (Turcz.) Maxim.
inferred← citeshttps://doi.org/10.1134/s1070363225606751openalex-snapshot
Synthesis of 3- and 3,6-Substituted Pyranocoumarins as Starting Structures Towards Compounds Having Neuroprotective Activity
inferred← citeshttps://doi.org/10.1155/2021/5965061openalex-snapshot
Phytochemical Analysis and Evaluation of Biological Activity of Lawsonia inermis Seeds Related to Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1186/s12906-021-03464-2openalex-snapshot
Phytochemical analysis and anticancer activity of Falcaria vulgaris Bernh growing in Moghan plain, northwest of Iran
inferred← citeshttps://doi.org/10.18311/jeoh/2022/29511openalex-snapshot
Therapeutic Efficacy of Natural Phytochemicals as Acetylcholinesterase Inhibitors Against Alzheimer’s Disease
inferred← citeshttps://doi.org/10.21203/rs.3.rs-530162/v1openalex-snapshot
Chemical Characterization and Evaluation of Anticancer Effect of Falcaria vulgaris via Induction of Apoptosis
inferred← citeshttps://doi.org/10.2174/0929867328666210827152914openalex-snapshot
Molecular Effects of Pteryxin and Scopoletin in the 5xFAD Alzheimer’s Disease Mouse Model
inferred← citeshttps://doi.org/10.2174/1386207323666200127145246openalex-snapshot
A Recent Look into Natural Products that have Potential to Inhibit Cholinesterases and Monoamine Oxidase B: Update for 2010-2019
inferred← citeshttps://doi.org/10.2174/1568026619666191203113745openalex-snapshot
Progress in Target Drug Molecules for Alzheimer's Disease
inferred← citeshttps://doi.org/10.2174/1568026620666200616142753openalex-snapshot
A Multi-layered Variable Selection Strategy for QSAR Modeling of Butyrylcholinesterase Inhibitors
inferred← citeshttps://doi.org/10.33320/maced.pharm.bull.2022.68.02.001openalex-snapshot
Phenolic phytochemicals for treatment of Alzheimer’s condition - a review
inferred← citeshttps://doi.org/10.33320/maced.pharm.bull.2022.68.04.016openalex-snapshot
Phytocomponents in treatment of Alzheimer condition
inferred← citeshttps://doi.org/10.3389/fbioe.2024.1387146openalex-snapshot
Rational design of a near-infrared fluorescent probe for monitoring butyrylcholinesterase activity and its application in development of inhibitors
inferred← citeshttps://doi.org/10.3389/fchem.2022.1063284openalex-snapshot
Butenolide derivatives from Aspergillus terreus selectively inhibit butyrylcholinesterase
inferred← citeshttps://doi.org/10.3389/fphar.2021.639651openalex-snapshot
Role of Plant-Derived Natural Compounds in Experimental Autoimmune Encephalomyelitis: A Review of the Treatment Potential and Development Strategy
inferred← citeshttps://doi.org/10.3389/fphar.2025.1698826openalex-snapshot
Pteryxin enhances human NK-cell cytotoxicity by upregulating NKp30, NKp46, and 2B4 via ERK/AKT signaling
inferred← citeshttps://doi.org/10.3390/molecules23092182openalex-snapshot
Natural Scaffolds with Multi-Target Activity for the Potential Treatment of Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/molecules26185582openalex-snapshot
Non-Alkaloid Cholinesterase Inhibitory Compounds from Natural Sources
inferred← citeshttps://doi.org/10.3390/molecules29020315openalex-snapshot
Benzofuran Derivatives from Cortex Mori Radicis and Their Cholinesterase-Inhibitory Activity
inferred← citeshttps://doi.org/10.3390/molecules29153514openalex-snapshot
Naturally Inspired Coumarin Derivatives in Alzheimer’s Disease Drug Discovery: Latest Advances and Current Challenges
inferred← citeshttps://doi.org/10.56238/globalhealthprespesc-039openalex-snapshot
Bibliometric study of chemical compounds based on medicinal plants anti-Alzheimer
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.