About: Pierre Champy

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

researcher (ORCID 0000-0003-2852-5098)

Attributes	Values
rdf:type	Item
description	wetenschapper (nl) дослідник (uk) professeur, phytochimie (fr) researcher (ORCID 0000-0003-2852-5098) (en)
rdfs:label	Pierre Champy (ca) Pierre Champy (en) Pierre Champy (fr) Pierre Champy (ast) Pierre Champy (nl) Pierre Champy (sl) Pierre Champy (sq)
skos:prefLabel	Pierre Champy (ca) Pierre Champy (en) Pierre Champy (fr) Pierre Champy (ast) Pierre Champy (nl) Pierre Champy (sl) Pierre Champy (sq)
name	Pierre Champy (ca) Pierre Champy (en) Pierre Champy (fr) Pierre Champy (ast) Pierre Champy (nl) Pierre Champy (sl) Pierre Champy (sq)
given name	wds:Q92166109-A690F553-0398-496A-8173-3C94FDBB1180
given name	Pierre
instance of	wds:Q92166109-F3366165-413F-4CEC-BF2A-8C22E89FABC9
instance of	Homo sapiens
occupation	wds:Q92166109-4c565dbc-49af-9523-5040-adb858e495cc wds:Q92166109-E712BC64-31AF-4000-B363-BA606E1D92C0
employer	wds:Q92166109-E60B245E-1F80-49D0-AE76-F6DC82CF1BED
languages spoken, written or signed	wds:Q92166109-3E6CB0EC-6B29-4D1D-90E4-9953CABBBEBD
sex or gender	wds:Q92166109-97eca2f7-4b2f-f0f9-788c-e0860a4c7251
ISNI	wds:Q92166109-29e88133-4d34-c347-33f1-e73fee5422f3
VIAF ID	wds:Q92166109-48445528-4376-ebe8-9449-d98cba5843cc
IdRef ID	wds:Q92166109-8f00eca3-4a2f-21eb-aae1-6338b20166fc
country of citizenship	wds:Q92166109-4e8c02d2-4df1-d3bd-23d7-e6dc96503fd7
date of birth	wds:Q92166109-eede974b-45aa-b9e2-3d1b-673364135dc9
family name	wds:Q92166109-1b1b243e-4ffb-f6c6-214f-ba1ebdb3e3a8
VIAF ID	http://viaf.org/viaf/204760617
IdRef ID	http://www.idref.fr/072308109/id
occupation	researcher pharmacist
employer	wd:Q51782390
languages spoken, written or signed	French
sex or gender	male
ISNI	000000035818655X
VIAF ID	204760617
IdRef ID	072308109
country of citizenship	France
date of birth	1977-01-01 00:00:00Z (xsd:dateTime)
family name	Champy
ORCID iD	wds:Q92166109-86E408F9-3501-4CC7-B776-81A55651D307
ORCID iD	https://orcid.org/0000-0003-2852-5098
ORCID iD	0000-0003-2852-5098
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q92166109
is author of	Labdane diterpenoids from Aframomum sceptrum: NMR study and antiparasitic activities Apolar Annonaceous acetogenins from the fruit pulp of Annona muricata. Annonacin, a lipophilic inhibitor of mitochondrial complex I, induces nigral and striatal neurodegeneration in rats: possible relevance for atypical parkinsonism in Guadeloupe Quantification of acetogenins in Annona muricata linked to atypical parkinsonism in guadeloupe. Annonacin, a natural mitochondrial complex I inhibitor, causes tau pathology in cultured neurons. "Squalenoylcurcumin" nanoassemblies as water-dispersible drug candidates with antileishmanial activity Structural study of acetogenins by tandem mass spectrometry under high and low collision energy Identification of the environmental neurotoxins annonaceous acetogenins in an Annona cherimolia Mill. Alcoholic Beverage Using HPLC-ESI-LTQ-Orbitrap. Chronic consumption of Annona muricata juice triggers and aggravates cerebral tau phosphorylation in wild-type and MAPT transgenic mice. Structural Characterisation of Acetogenins from Annona muricata by Supercritical Fluid Chromatography Coupled to High-Resolution Tandem Mass Spectrometry. A new adjacent bis-tetrahydrofuran annonaceous acetogenin from the seeds of Uvaria chamae Tryptamine-derived alkaloids from Annonaceae exerting neurotrophin-like properties on primary dopaminergic neurons Medicinal plants and finished marketed herbal products used in the treatment of malaria in the Ashanti region, Ghana Bioactive phloroglucinols from Mallotus oppositifolius. MALDI-TOF MS profiling of annonaceous acetogenins in Annona muricata products for human consumption Revisiting Previously Investigated Plants: A Molecular Networking-Based Study of Geissospermum laeve. Method development for quantification of the environmental neurotoxin annonacin in Rat plasma by UPLC-MS/MS and application to a pharmacokinetic study. Composition, and antimicrobial and remarkable antiprotozoal activities of the essential oil of rhizomes of Aframomum sceptrum K. Schum. (Zingiberaceae). Characterization of the Annonaceous acetogenin, annonacinone, a natural product inhibitor of plasminogen activator inhibitor-1. 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 Comprehensive characterization of Annonaceous acetogenins within a complex extract by HPLC-ESI-LTQ-Orbitrap® using post-column lithium infusion 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 Corynanthean-Epicatechin Flavoalkaloids from Corynanthe pachyceras Phenylpropane as an Alternative Dearomatizing Unit of Indoles: Discovery of Inaequalisines A and B Using Substructure-Informed Molecular Networking Annonacin, a natural lipophilic mitochondrial complex I inhibitor, increases phosphorylation of tau in the brain of FTDP-17 transgenic mice Quantification of the environmental neurotoxin annonacin in Rat brain by UPLC-MS/MS. Antiplasmodial Securinega alkaloids from Phyllanthus fraternus : Discovery of natural (+)-allonorsecurinine Cassane diterpenoids from stem bark of Erythrophleum suaveolens [(Guill. et Perr.), Brenan] 1 H qNMR Quantification of Annonaceous Acetogenins in Crude Extracts of Annona muricata L. Fruit Pulp. Five new cassane diterpenes from the seeds and bark of Erythrophleum suaveolens Chemicals possessing a neurotrophin-like activity on dopaminergic neurons in primary culture Comments on EFSA's opinion about the health claim “improvement of bowel function” for hydroxyanthracenic derivatives Antiplasmodial activity of selected medicinal plants used to treat malaria in Ghana Validation data for the quantification of the Annonaceous acetogenin annonacin in Rat brain by UPLC-MS/MS. Pyrone and unusually furanone-substituted flavones from the leaves of Hoslundia opposita. CANPA: Computer-Assisted Natural Products Anticipation Streamlined targeting of Amaryllidaceae alkaloids from the bulbs of Crinum scillifolium using spectrometric and taxonomically-informed scoring metabolite annotations Spectroscopic data of new cassane diterpenoids from the root bark of Erythrophleum suaveolens Antifungal and Anthelmintic Activities ofCleistopholis patens(Annonaceae)

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