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Cytotoxic Guanidine Alkaloids from Pterogyne nitens
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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/ardp.19632960805openalex-snapshot
Arginin als Vorstufe von Galegin in Galega officinalis L. Zur Biochemie und Physiologie von Galegin in Galega officinalis L., III. Mitt.
inferredcites →https://doi.org/10.1016/0022-1759(83)90303-4openalex-snapshot
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
inferredcites →https://doi.org/10.1016/0031-9422(82)80021-6openalex-snapshot
Galegine and a new dihydroxyalkylacetamide from Verbesina enceloiodes
inferredcites →https://doi.org/10.1016/j.phytochem.2005.04.043openalex-snapshot
Benzopyrans from Curvularia sp., an endophytic fungus associated with Ocotea corymbosa (Lauraceae)
inferredcites →https://doi.org/10.1016/j.phytochem.2008.01.006openalex-snapshot
Flavonols from Pterogyne nitens and their evaluation as myeloperoxidase inhibitors
inferredcites →https://doi.org/10.1016/s0021-9258(18)76920-2openalex-snapshot
A MODIFICATION OF SAKAGUCHI'S REACTION FOR THE QUANTITATIVE DETERMINATION OF ARGININE
inferredcites →https://doi.org/10.1016/s0040-4020(01)88940-7openalex-snapshot
Alchornéine, isoalchornéine et alchornéinone, produits isolés de l'Alchornea floribunda Muell. Arg.
inferredcites →https://doi.org/10.1021/ja00130a005openalex-snapshot
Martinelline and Martinellic Acid, Novel G-Protein Linked Receptor Antagonists from the Tropical Plant Martinella iquitosensis (Bignoniaceae)
inferredcites →https://doi.org/10.1021/jo0103423openalex-snapshot
Celogentins A−C, New Antimitotic Bicyclic Peptides from the Seeds of Celosia argentea
inferredcites →https://doi.org/10.1021/np050066dopenalex-snapshot
Cimipronidine, a Cyclic Guanidine Alkaloid from Cimicifuga racemosa
inferredcites →https://doi.org/10.1021/np50125a006openalex-snapshot
Bioactive Guanidine Alkaloids from Pterogyne nitens
inferredcites →https://doi.org/10.1021/np980015zopenalex-snapshot
Fontaineine, a New Alkaloid from Fontainea pancheri
inferredcites →https://doi.org/10.1039/c29690001484openalex-snapshot
Hexahydroimidazo-pyrimidines, a new class of alkaloids from Alchornea javanensis
inferredcites →https://doi.org/10.1080/14786410412331271979openalex-snapshot
Cytotoxic lignans from the stems ofStyrax camporum(Styracaceae)
inferredcites →https://doi.org/10.1186/1746-4269-2-1openalex-snapshot
The lunar-tide cycle viewed by crustacean and mollusc gatherers in the State of Paraíba, Northeast Brazil and their influence in collection attitudes
inferredcites →https://doi.org/10.1248/cpb.56.723openalex-snapshot
Myeloperoxidase Inhibitory and Radical Scavenging Activities of Flavones from Pterogyne nitens
inferredcites →https://doi.org/10.1590/s0100-40422008000400018openalex-snapshot
Constituintes químicos das flores de Pterogyne nitens (Caesalpinioideae)
inferredcites →https://doi.org/10.2174/0929867033456990openalex-snapshot
Novel Hypotensive Agents from Verbesina Caracasana: Structure, Synthesis and Pharmacology
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/phytokeys.240.101716zenodo-depositor-declared
Advances in Legume Systematics 14. Classification of Caesalpinioideae. Part 2: Higher-level classification
inferred← citeshttps://doi.org/10.1002/ange.201602971openalex-snapshot
Cyclic Guanidine Compounds from Toxic Newts Support the Hypothesis that Tetrodotoxin is Derived from a Monoterpene
inferred← citeshttps://doi.org/10.1002/anie.201602971openalex-snapshot
Cyclic Guanidine Compounds from Toxic Newts Support the Hypothesis that Tetrodotoxin is Derived from a Monoterpene
inferred← citeshttps://doi.org/10.1002/ardp.201000363openalex-snapshot
The Application of Tandem Aza‐Wittig Reaction to Synthesize Artemisinin–Guanidine Hybrids and Their Anti‐Tumor Activity
inferred← citeshttps://doi.org/10.1002/ddr.22180openalex-snapshot
A review of natural products and small‐molecule therapeutics acting on central nervous system malignancies: Approaches for drug development, targeting pathways, clinical trials, and challenges
inferred← citeshttps://doi.org/10.1007/978-1-61779-624-1_7openalex-snapshot
Isolation of Natural Products by Low-Pressure Column Chromatography
inferred← citeshttps://doi.org/10.1007/978-3-642-22144-6_48openalex-snapshot
Antiangiogenic Alkaloids from Plants
inferred← citeshttps://doi.org/10.1007/s10616-013-9590-2openalex-snapshot
Nitensidine A, a guanidine alkaloid from Pterogyne nitens, induces osteoclastic cell death
inferred← citeshttps://doi.org/10.1007/s12039-014-0723-8openalex-snapshot
First total synthesis of a guanidine alkaloid Nitensidine D using immobilized ionic liquid, microwaves and formamidinesulfinic acid
inferred← citeshttps://doi.org/10.1007/s13277-010-0064-2openalex-snapshot
Alkaloids extracted from Pterogyne nitens induce apoptosis in malignant breast cell line
inferred← citeshttps://doi.org/10.1016/b978-0-323-91250-1.00010-0openalex-snapshot
Recent advances in natural product-based anticancer agents
inferred← citeshttps://doi.org/10.1016/bs.alkal.2021.11.001openalex-snapshot
Synthesis of pyrimidine-containing alkaloids
inferred← citeshttps://doi.org/10.1016/j.apjtb.2016.08.003openalex-snapshot
Anti-Candida and anti-Cryptococcus evaluation of 15 non-alkaloidal compounds from Pterogyne nitens
inferred← citeshttps://doi.org/10.1016/j.exppara.2023.108542openalex-snapshot
Nematostatic activity of isoprenylated guanidine alkaloids from Pterogyne nitens and their interaction with acetylcholinesterase
inferred← citeshttps://doi.org/10.1016/j.phymed.2013.08.024openalex-snapshot
Nitensidine A, a guanidine alkaloid from Pterogyne nitens, is a novel substrate for human ABC transporter ABCB1
inferred← citeshttps://doi.org/10.1016/j.phymed.2018.05.016openalex-snapshot
Nitensidine B affects proteins of the glycolytic pathway and induces apoptosis in cervical carcinoma cells immortalized by HPV16
inferred← citeshttps://doi.org/10.1016/j.phymed.2025.156850openalex-snapshot
Potential of phytochemicals for pharmacotherapy of glioblastoma multiforme: Progress, pitfalls, and promise
inferred← citeshttps://doi.org/10.1016/j.tet.2014.03.087openalex-snapshot
Iodocyclisations reactions of Boc- and Cbz-protected N-allylguanidines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.09.093openalex-snapshot
Intramolecular palladium mediated π-allyl cyclisation of bis-Cbz- and bis-Boc-protected guanidines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.01.100openalex-snapshot
Facile solid phase synthesis of N-cycloguanidinyl-formyl peptides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.10.140openalex-snapshot
Synthesis of the cyclic prenylguanidine nitensidine E using a palladium-catalyzed carbenylative amination
inferred← citeshttps://doi.org/10.1021/acs.analchem.6b02388openalex-snapshot
Online Extraction Coupled to Liquid Chromatography Analysis (OLE-LC): Eliminating Traditional Sample Preparation Steps in the Investigation of Solid Complex Matrices
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00623openalex-snapshot
Structures of N -Hydroxy-Type Tetrodotoxin Analogues and Bicyclic Guanidinium Compounds Found in Toxic Newts
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00368openalex-snapshot
Plantadeprate A, a Tricyclic Monoterpene Zwitterionic Guanidium, and Related Derivatives from the Seeds of Plantago depressa
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00256openalex-snapshot
Analogues of Marine Guanidine Alkaloids Are in Vitro Effective against Trypanosoma cruzi and Selectively Eliminate Leishmania (L.) infantum Intracellular Amastigotes
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00941openalex-snapshot
Marine Terpenoid Diacylguanidines: Structure, Synthesis, and Biological Evaluation of Naturally Occurring Actinofide and Synthetic Analogues
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00916openalex-snapshot
Identification of Tricyclic Guanidino Compounds from the Tetrodotoxin-Bearing Newt Taricha granulosa
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01408openalex-snapshot
Rhodium-Catalyzed Regioselective Synthesis of Isocoumarins through Benzothiadiazine-Fused Frameworks
inferred← citeshttps://doi.org/10.1021/acschembio.3c00083openalex-snapshot
Bioactive Natural Product Discovery via Deuterium Adduct Bioactivity Screening
inferred← citeshttps://doi.org/10.1021/np400235sopenalex-snapshot
Guanidine Alkaloids from Plumbago zeylanica
inferred← citeshttps://doi.org/10.1021/np500281copenalex-snapshot
In Vitro Antibacterial Activity of Prenylated Guanidine Alkaloids from Pterogyne nitens and Synthetic Analogues
inferred← citeshttps://doi.org/10.1021/np900288xopenalex-snapshot
An Antimicrobial Guanidine-Bearing Sesterterpene from the Cultured Cyanobacterium Scytonema sp.
inferred← citeshttps://doi.org/10.1021/np900309popenalex-snapshot
Cytotoxic Neoclerodane Diterpenoids from Scutellaria barbata
inferred← citeshttps://doi.org/10.1021/ol301385gopenalex-snapshot
Carbenylative Amination with N-Tosylhydrazones
inferred← citeshttps://doi.org/10.1039/b507874copenalex-snapshot
The chemistry and biology of organic guanidine derivatives
inferred← citeshttps://doi.org/10.1039/c0np00016gopenalex-snapshot
The chemistry and biology of organic guanidine derivatives
inferred← citeshttps://doi.org/10.1271/kagakutoseibutsu.60.440openalex-snapshot
陸棲イモリが有する神経毒テトロドトキシンの謎
inferred← citeshttps://doi.org/10.15212/amm-2024-0088openalex-snapshot
Biologically active guanidine alkaloids
inferred← citeshttps://doi.org/10.1590/s0102-695x2009000300013openalex-snapshot
Tratamento crônico com extrato alcoólico de Pterogyne nitens não melhora parâmetros clássicos do diabetes experimental
inferred← citeshttps://doi.org/10.1590/s0102-695x2010005000017openalex-snapshot
Antimicrobial activity of Pterogyne nitens Tul., Fabaceae, against opportunistic fungi
inferred← citeshttps://doi.org/10.1590/s1516-05722012000400014openalex-snapshot
Avaliação das atividades antioxidante, anti e pró-hemolítica do extrato etanólico das folhas de Pterogyne nitens Tul. (Fabaceae-Caesalpinioideae)
inferred← citeshttps://doi.org/10.2174/1871520615666150113103439openalex-snapshot
Development of Fourth Generation ABC Inhibitors from Natural Products: A Novel Approach to Overcome Cancer Multidrug Resistance
inferred← citeshttps://doi.org/10.3233/bme-151282openalex-snapshot
Human ABCB1 confers cells resistance to cytotoxic guanidine alkaloids from Pterogyne nitens
inferred← citeshttps://doi.org/10.5740/jaoacint.11-137openalex-snapshot
Fast Screening for Antioxidant Properties of Flavonoids from Pterogyne nitens Using Electrochemical Methods
inferred← citeshttps://doi.org/10.5897/jmpr10.094openalex-snapshot
Alcohol extract of Pterogyne nitens leaves fails to reduce severity of streptozotocin-induced diabetes in rats
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