About: Erwan Poupon

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) araştırmacı (tr) chercheur (fr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh)
rdfs:label	Erwan Poupon (en) Erwan Poupon (es) Erwan Poupon (fr) Erwan Poupon (nl) Erwan Poupon (ast)
skos:prefLabel	Erwan Poupon (en) Erwan Poupon (es) Erwan Poupon (fr) Erwan Poupon (nl) Erwan Poupon (ast)
name	Erwan Poupon (en) Erwan Poupon (es) Erwan Poupon (fr) Erwan Poupon (nl) Erwan Poupon (ast)
Scopus author ID	wds:Q58808567-D66277FB-464D-4315-A1D4-B05194087359
Scopus author ID	6603263844
given name	wds:Q58808567-E5697D93-DD16-44F8-9C05-72B41BD570FC
given name	Erwan
instance of	wds:Q58808567-7393EC7D-6B30-43AA-971D-9CF0ADEBF435
instance of	Homo sapiens
doctoral student	wds:Q58808567-22E909DC-DFE0-4D22-930D-9B7A6EC9362C wds:Q58808567-EB18654A-5206-4627-9759-F98CCD82A697
doctoral student	Edmond Gravel Charlotte Fox Alcover
occupation	wds:Q58808567-41A81360-8CDA-4C5B-84F7-6661E0B73B56
employer	wds:Q58808567-EDA398C4-92D4-4EC0-BFC7-99372C519D7C
NUKAT ID	wds:Q58808567-0EDE7456-7E18-44CE-A0F5-D09B9C41FE23
sex or gender	wds:Q58808567-38703bba-59f0-46fc-ade4-1004e50b1d59
ISNI	wds:Q58808567-8F9463B2-5BE1-49D1-8E9B-C84230445D02
VIAF ID	wds:Q58808567-32FB4A80-F99C-4A43-AE78-685D580C85C5
GND ID	wds:Q58808567-f7cae481-8f4c-4921-8ebc-7bcf7c884af3
Bibliothèque nationale de France ID	wds:Q58808567-FF5803CC-25EC-4310-9C9F-AD20F6414864
IdRef ID	wds:Q58808567-CF65A944-6B15-4E74-B6FF-988F0AEB9F07
family name	wds:Q58808567-4D2AE659-2D78-4211-9312-951FF030E956
National Library of Israel J9U ID	wds:Q58808567-32E28078-93ED-43BF-8A6E-1080FA25F62C
VIAF ID	http://viaf.org/viaf/160331120
GND ID	https://d-nb.info/gnd/142834599
Bibliothèque nationale de France ID	http://data.bnf.fr/ark:/12148/cb170580541#about
IdRef ID	http://www.idref.fr/110147561/id
occupation	researcher
employer	University of Paris-Sud
NUKAT ID	n2011214423
sex or gender	male
ISNI	0000000119429307
VIAF ID	160331120
GND ID	142834599
Bibliothèque nationale de France ID	170580541
IdRef ID	110147561
family name	Poupon
National Library of Israel J9U ID	987007371177805171
ORCID iD	wds:Q58808567-A70C4A3E-3E98-47B8-84DE-A7257F040468
ORCID iD	https://orcid.org/0000-0002-1178-6083
ORCID iD	0000-0002-1178-6083
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58808567
is author of	Labdane diterpenoids from Aframomum sceptrum: NMR study and antiparasitic activities "Squalenoylcurcumin" nanoassemblies as water-dispersible drug candidates with antileishmanial activity Biogenetic hypothesis and first steps towards a biomimetic synthesis of haouamines Alkaloids from Rutaceae: activities of canthin-6-one alkaloids and synthetic analogues on glioblastoma stems cells Extraction, hemisynthesis, and synthesis of canthin-6-one analogues. Evaluation of their antifungal activities Semisynthesis and screening of a small library of pro-apoptotic squamocin analogues: selection and study of a benzoquinone hybrid with an improved biological profile. Highly cytotoxic and neurotoxic acetogenins of the Annonaceae: new putative biological targets of squamocin detected by activity-based protein profiling. Annonaceous acetogenins: the hydroxyl groups and THF rings are crucial structural elements for targeting the mitochondria, demonstration with the synthesis of fluorescent squamocin analogues. Remarkable substituent effect: beta-aminosquamocin, a potent dual inhibitor of mitochondrial complexes I and III. Effects of canthin-6-one alkaloids from Zanthoxylum chiloperone on Trypanosoma cruzi-infected mice DNA-Templated [2+2] Photocycloaddition: A Straightforward Entry into the Aplysinopsin Family of Natural Products Unified biomimetic assembly of voacalgine A and bipleiophylline via divergent oxidative couplings. New building blocks for tackling the synthesis of polyhydroxylated piperidines: expeditious synthesis of amino derivatives in the 1-deoxynojirimycin series Synthesis of polyhydroxylated piperidines and evaluation as glycosidase inhibitors Revisiting Previously Investigated Plants: A Molecular Networking-Based Study of Geissospermum laeve. Composition, and antimicrobial and remarkable antiprotozoal activities of the essential oil of rhizomes of Aframomum sceptrum K. Schum. (Zingiberaceae). An Expeditious Total Synthesis of the Natural Stereomeric Mixture of Stenusine Following a Possible Biogenetic Pathway We are grateful to Prof. Dr. Dieter Enders for fruitful discussions Manipulating Simple Reactive Chemical Units: Fishing for Alkaloids from Complex Mixtures Unified synthesis of quinone sesquiterpenes based on a radical decarboxylation and quinone addition reaction Synthesis of (-)-ilimaquinone via a radical decarboxylation and quinone addition reaction Insights into the Biosynthesis of Cyclic Guanidine Alkaloids from Crambeidae Marine Sponges Collected mass spectrometry data on monoterpene indole alkaloids from natural product chemistry research CANPA: Computer-Assisted Natural Products Anticipation Natural products targeting strategies involving molecular networking: different manners, one goal Pleiokomenines A and B: Dimeric Aspidofractinine Alkaloids Tethered with a Methylene Group. Theionbrunonines A and B: Dimeric Vobasine Alkaloids Tethered by a Thioether Bridge from Mostuea brunonis Molecular Networking Reveals Serpentinine-Related Bisindole Alkaloids from Picralima nitida, a Previously Well-Investigated Species Phenylpropane as an Alternative Dearomatizing Unit of Indoles: Discovery of Inaequalisines A and B Using Substructure-Informed Molecular Networking Voatriafricanines A and B, Trimeric Vobasine-Aspidosperma-Aspidosperma Alkaloids from Voacanga africana An Unprecedented Blue Chromophore Found in Nature using a "Chemistry First" and Molecular Networking Approach: Discovery of Dactylocyanines A-H. Biogenetic relationships between Annonaceous acetogenins: squamocin is not a precursor of chamuvarinin based on a semisynthetic study Solid-State Electrochemical Assay of Heme-Binding Molecules for Screening of Drugs with Antimalarial Potential

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