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Targeted Isolation of Monoterpene Indole Alkaloids from Palicourea sessilis

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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/hlca.201300050openalex-snapshot
Two New Indole Alkaloids from Emmenopterys henryi
inferredcites →https://doi.org/10.1007/s12272-012-0320-7openalex-snapshot
In vitro antiproliferative effects of the indole alkaloid vallesiachotamine on human melanoma cells
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/10.1016/0031-9422(94)00823-copenalex-snapshot
Alkaloids and other compounds from Psychotria correae
inferredcites →https://doi.org/10.1016/j.bjp.2015.07.002openalex-snapshot
The catechol-O-methyltransferase inhibitory potential of Z-vallesiachotamine by in silico and in vitro approaches
inferredcites →https://doi.org/10.1016/j.bse.2014.04.013openalex-snapshot
Terpenoids and a coumarin from aerial parts of Psychotria vellosiana Benth. (Rubiaceae)
inferredcites →https://doi.org/10.1016/j.chroma.2016.07.030openalex-snapshot
The use of chemometrics to study multifunctional indole alkaloids from Psychotria nemorosa (Palicourea comb. nov.). Part I: Extraction and fractionation optimization based on metabolic profiling
inferredcites →https://doi.org/10.1016/j.chroma.2016.08.005openalex-snapshot
The use of chemometrics to study multifunctional indole alkaloids from Psychotria nemorosa (Palicourea comb. nov.). Part II: Indication of peaks related to the inhibition of butyrylcholinesterase and monoamine oxidase-A
inferredcites →https://doi.org/10.1016/j.ejps.2007.10.004openalex-snapshot
In vitro screening assays to identify natural or synthetic acetylcholinesterase inhibitors: Thin layer chromatography versus microplate methods
inferredcites →https://doi.org/10.1016/j.phytochem.2012.11.015openalex-snapshot
Indole alkaloids of Psychotria as multifunctional cholinesterases and monoamine oxidases inhibitors
inferredcites →https://doi.org/10.1016/j.phytochem.2015.05.013openalex-snapshot
Loganin and secologanin derived tryptamine–iridoid alkaloids from Palicourea crocea and Palicourea padifolia (Rubiaceae)
inferredcites →https://doi.org/10.1016/j.phytol.2008.10.007openalex-snapshot
Monoterpenoid indole alkaloids from Palicourea crocea
inferredcites →https://doi.org/10.1016/j.tetlet.2014.06.090openalex-snapshot
Three new monoterpene indole alkaloids from Psychotria umbellata Thonn.
inferredcites →https://doi.org/10.1016/j.trac.2016.02.021openalex-snapshot
Enlarging the bottleneck in the analysis of alkaloids: A review on sample preparation in herbal matrices
inferredcites →https://doi.org/10.1016/s0031-9422(96)00646-2openalex-snapshot
Confirmation of the absolute configuration of dolichantoside and isodolichantoside by synthesis from (−)-secologanin
inferredcites →https://doi.org/10.1016/s0031-9422(99)00215-0openalex-snapshot
β-Carboline monoterpenoid glucosides from Palicourea adusta
inferredcites →https://doi.org/10.1016/s0040-4039(98)01686-4openalex-snapshot
Final solution on the long-standing structural arguments on the C-3 stereochemistries of three glucoindole alkaloids: Palicoside, dolichantoside, and isodolichantoside — through chemical conversions and spectroscopic studies
inferredcites →https://doi.org/10.1016/s0305-1978(01)00059-xopenalex-snapshot
Indole monoterpene alkaloids from leaves of Psychotria suterella Müll. Arg. (Rubiaceae)
inferredcites →https://doi.org/10.1021/acs.analchem.5b04804openalex-snapshot
Integration of Molecular Networking and In-Silico MS/MS Fragmentation for Natural Products Dereplication
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b01013openalex-snapshot
Revisiting Previously Investigated Plants: A Molecular Networking-Based Study ofGeissospermum laeve
inferredcites →https://doi.org/10.1021/jo00134a027openalex-snapshot
Constituents of Zanthoxylum. 7. Old and new alkaloids from Zanthoxylum arborescens
inferredcites →https://doi.org/10.1021/jo900408dopenalex-snapshot
Assigning the Stereochemistry of Pairs of Diastereoisomers Using GIAO NMR Shift Calculation
inferredcites →https://doi.org/10.1021/np000590eopenalex-snapshot
Brachycerine, a Novel Monoterpene Indole Alkaloid from Psychotria brachyceras
inferredcites →https://doi.org/10.1021/np0703951openalex-snapshot
Psychollatine, a Glucosidic Monoterpene Indole Alkaloid from Psychotria umbellata
inferredcites →https://doi.org/10.1021/np400413sopenalex-snapshot
Molecular Networking as a Dereplication Strategy
inferredcites →https://doi.org/10.1021/np9701642openalex-snapshot
Pyrrolidinoindoline Alkaloids from Psychotria colorata
inferredcites →https://doi.org/10.1021/pr400230popenalex-snapshot
Spectral Library Generating Function for Assessing Spectrum-Spectrum Match Significance
inferredcites →https://doi.org/10.1038/nbt.3597openalex-snapshot
Sharing and community curation of mass spectrometry data with Global Natural Products Social Molecular Networking
inferredcites →https://doi.org/10.1055/s-0034-1383261openalex-snapshot
Alkaloids from Psychotria Target Sirtuins: In Silico and In Vitro Interaction Studies
inferredcites →https://doi.org/10.1093/bioinformatics/btn323openalex-snapshot
ProteoWizard: open source software for rapid proteomics tools development
inferredcites →https://doi.org/10.1177/1934578x1601100920openalex-snapshot
Multifunctional Monoamine Oxidases and Cholinesterases Inhibitory Effects, as well as UPLC-DAD-MS Chemical Profile of Alkaloid Fractions Obtained from Species of the Palicoureeae Tribe
inferredcites →https://doi.org/10.2174/1568026614666140324142409openalex-snapshot
Indole Alkaloids and Semisynthetic Indole Derivatives as Multifunctional Scaffolds Aiming the Inhibition of Enzymes Related to Neurodegenerative Diseases – A Focus on Psychotria L. Genus
inferredcites →https://doi.org/10.3109/14756366.2012.666536openalex-snapshot
Monoamine oxidase inhibition by monoterpene indole alkaloids and fractions obtained from Psychotria suterella and Psychotria laciniata
inferredcites →https://doi.org/10.3417/2012003openalex-snapshot
Rubiacearum Americanarum Magna Hama XXXIII: The New GroupPalicoureasect.Didymocarpaewith Four New Species and Two New Subspecies (Palicoureeae)
inferredcites →https://doi.org/10.3417/2015001openalex-snapshot
Rubiacearum Americanarum Magna Hama Pars XXXIV: The New GroupPalicoureasect.Tricephaliumwith Eight New Species and a New Subspecies (Palicoureeae)

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.2021.112821zenodo-depositor-declared
Cruciasides C-G, monoterpenoid glycosides from Cruciata articulata
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inferred← citeshttps://doi.org/10.1007/978-981-13-9871-1_13openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11101-021-09769-xopenalex-snapshot
A revised classification of the sister tribes Palicoureeae and Psychotrieae (Rubiaceae) indicates genus-specific alkaloid accumulation
inferred← citeshttps://doi.org/10.1007/s11306-021-01833-zopenalex-snapshot
In vitro antiplasmodial activity, targeted LC–MS metabolite profiling, and identification of major natural products in the bioactive extracts of Palicourea and Psychotria species from the Amazonia and Atlantic Forest biomes, Brazil
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2019.01.004openalex-snapshot
Current status and contemporary approaches to the discovery of antitumor agents from higher plants
inferred← citeshttps://doi.org/10.1016/j.bse.2020.104114openalex-snapshot
Dereplication of Palicourea sessilis ethanol extracts by UPLC-DAD-ESI-MS/MS discloses the presence of hydroxycinnamic acid amides and the absence of monoterpene indole alkaloids
inferred← citeshttps://doi.org/10.1016/j.chroma.2021.461935openalex-snapshot
Offline preparative three-dimensional HPLC for systematic and efficient purification of alkaloids from Gelsemium elegans Benth
inferred← citeshttps://doi.org/10.1016/j.fct.2022.113340openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104558openalex-snapshot
Indole alkaloids: 2012 until now, highlighting the new chemical structures and biological activities
inferred← citeshttps://doi.org/10.1016/j.mib.2018.08.004openalex-snapshot
Opportunities for plant natural products in infection control
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112296openalex-snapshot
Alkaloid and iridoid glucosides from Palicourea luxurians (Rubiaceae: Palicoureeae) indicate tryptamine- and tryptophan-iridoid alkaloid formation apart the strictosidine pathway
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151354openalex-snapshot
Scholarinine A, a N3 type caged-monoterpene indole alkaloid as Cav3.1 T-type calcium channel inhibitor from Alstonia scholaris
inferred← citeshttps://doi.org/10.1016/s1875-5364(22)60216-4openalex-snapshot
Targeted isolation and identification of bioactive pyrrolidine alkaloids from Codonopsis pilosula using characteristic fragmentation-assisted mass spectral networking
inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c00922openalex-snapshot
Ethnobotany and the Role of Plant Natural Products in Antibiotic Drug Discovery
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00676openalex-snapshot
Polyhalogenation of Isoflavonoids by the Termite-Associated Actinomadura sp. RB99
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c01069openalex-snapshot
Cyclotides from Brazilian Palicourea sessilis and Their Effects on Human Lymphocytes
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00094openalex-snapshot
Feature-Based Molecular Networking Discovery of Bromopyrrole Alkaloids from the Marine Sponge Agelas dispar
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00292openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00469openalex-snapshot
Bioactive Azepine-Indole Alkaloids from Psychotria nemorosa
inferred← citeshttps://doi.org/10.1038/s41467-024-51765-0openalex-snapshot
Asymmetric N-oxidation catalyzed by bisguanidinium dinuclear oxodiperoxomolybdosulfate
inferred← citeshttps://doi.org/10.1039/c9np00006bopenalex-snapshot
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inferred← citeshttps://doi.org/10.1055/a-1375-6456openalex-snapshot
Extraction and Fractionation Effects on Antiplasmodial Activity and Phytochemical Composition of Palicourea hoffmannseggiana
inferred← citeshttps://doi.org/10.1080/14786419.2021.1961135openalex-snapshot
Stephtetrandrine A-D, bisbenzylisoquinoline alkaloids from Stephania tetrandra
inferred← citeshttps://doi.org/10.1080/14786419.2024.2449510openalex-snapshot
The genus Palicourea Aubl. (Rubiaceae): source of bioactive compounds
inferred← citeshttps://doi.org/10.1515/znc-2022-0234openalex-snapshot
Structure elucidation of an aspidofractinine-type monoterpene indole alkaloid from Melodinus reticulatus
inferred← citeshttps://doi.org/10.21829/abm131.2024.2405openalex-snapshot
Phenolic and volatile compounds, total protein content, antioxidant and antidiabetic activities of leaves of Palicourea padifolia (Rubiaceae)
inferred← citeshttps://doi.org/10.24820/ark.5550190.p010.464openalex-snapshot
A formal approach to the cyanobacterial sunscreen indole, prenostodione
inferred← citeshttps://doi.org/10.3389/fmolb.2023.1238475openalex-snapshot
Application of feature-based molecular networking and MassQL for the MS/MS fragmentation study of depsipeptides
inferred← citeshttps://doi.org/10.3389/fnins.2022.826289openalex-snapshot
Azepine-Indole Alkaloids From Psychotria nemorosa Modulate 5-HT2A Receptors and Prevent in vivo Protein Toxicity in Transgenic Caenorhabditis elegans
inferred← citeshttps://doi.org/10.3389/fphar.2020.00397openalex-snapshot
Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes
inferred← citeshttps://doi.org/10.3390/molecules26010230openalex-snapshot
Application of HPLC-DAD for In Vitro Investigation of Acetylcholinesterase Inhibition Activity of Selected Isoquinoline Alkaloids from Sanguinaria canadensis Extracts
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