About: Pascale Moreau

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An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Moreau, Pascale (19..-.... ; chercheuse en chimie organique et médicinale) Moreau, Pascale (19..-.... ; chercheuse en chimie organique et médicinale)
Life Event	http://www.idref.fr/142933651/birth
preferred label	Moreau, Pascale (19..-.... ; chercheuse en chimie organique et médicinale)
name	Pascale Moreau
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/fra
Given name	Pascale
familyName	Moreau
note	Professeur au département de chimie, membre du laboratoire Synthèse Et Etude de Systèmes à Intérêt Biologique, SEESIB, UMR 6504, en 2011 (Université Blaise Pascal, Clermont-Ferrand 2) Professeur des universités en poste à l'Université Clermont Auvergne. Membre de l'ICCF-Institut de Chimie de Clermont-Ferrand (en 2018) Auteur d'une thèse de doctorat en chimie à l'Université d'Orléans en 1993
gender	female
ORCID iD	0000-0001-6527-7586
Scopus ID	7201395136
is sameAs of	Moreau, Pascale (19..-.... ; chercheuse en chimie organique et médicinale) Moreau, Pascale (19..-.... ; chercheuse en chimie organique et médicinale)
is Thesis advisor of	Synthèse de composés hétérocycliques aromatiques azotés, inhibiteurs potentiels de kinases http://www.sudoc.fr/20178341X/id http://www.sudoc.fr/139802568/id http://www.sudoc.fr/144481634/id Synthèse de composés aromatiques, anticancéreux potentiels, modulateurs des voies de signalisation de l'apoptose http://www.sudoc.fr/247172928/id Etude de la fonctionnalisation de thiazolo[5,4-f]quinazolin-9(8H)-ones via des sel de diaryliodonium et synthèse de nouvelles thiazolo[4,5-g]quinazolin-8(7H)-ones, potentiels inhibiteurs de kinases. http://www.sudoc.fr/277397286/id http://www.sudoc.fr/247141585/id http://www.sudoc.fr/282462031/id
is Praeses of	http://www.sudoc.fr/193720701/id http://www.sudoc.fr/229091911/id http://www.sudoc.fr/155480758/id http://www.sudoc.fr/278417477/id http://www.sudoc.fr/224289578/id http://www.sudoc.fr/269110909/id http://www.sudoc.fr/230293077/id http://www.sudoc.fr/276756681/id http://www.sudoc.fr/278993168/id
is Author of	http://www.sudoc.fr/043923445/id Synthesis, Pim kinase inhibitory potencies and in vitro antiproliferative activities of diversely substituted pyrrolo[2,3-a]carbazoles. , , 30 juin-2 juillet 2010. Synthesis, Pim kinase inhibitory potencies and in vitro antiproliferative activities of diversely substituted pyrrolo[2,3-a]carbazoles Functionalization of 9-thioxanthone at the 1-position: From arylamino derivatives to [1]benzo(thio)pyrano[4,3,2-de]benzothieno[2,3-b]quinolines of biological interest Syntheses and Biological Evaluation of Indolocarbazoles, Analogues ofRebeccamycin, Modified at the Imide Heterocycle Synthesis, Mode of Action, and Biological Activities of Rebeccamycin BromoDerivatives Synthesis, protein kinase inhibitory potencies and in vitro antiproliferative activities of meridianin derivatives. Rebeccamycin derivatives as dual DNA damaging agents and potent checkpoint kinase 1 inhibitors. Improved potency of pyridin-2(1H)one derivatives for the treatment of mechanical allodynia Syntheses and Biological Activities of Rebeccamycin Analogues. Introduction ofa Halogenoacetyl Substituent Synthesis and biological activities of new di- and trimeric quinoline derivatives Triple Helix-Forming Oligonucleotides Conjugated toIndolocarbazole Poisons Direct Topoisomerase I-Mediated DNACleavage to a Specific Site Identification of pyrrolo[2,3-g]indazoles as new Pim kinase inhibitors. New pyrido[3,4-g]quinazoline derivatives as CLK1 and DYRK1A inhibitors: synthesis, biological evaluation and binding mode analysis Syntheses and Biological Activities (Topoisomerase Inhibition and Antitumorand Antimicrobial Properties) of Rebeccamycin Analogues Bearing ModifiedSugar Moieties and Substituted on the Imide Nitrogen with a Methyl Group http://www.sudoc.fr/246215291/id Syntheses and Antiproliferative Activities of New Rebeccamycin Derivativeswith the Sugar Unit Linked to Both Indole Nitrogens Synthesis and biological activities of polyquinoline derivatives: new Bcl-2 family protein modulators. Kinase inhibitions in pyrido[4,3-h] and [3,4-g]quinazolines: Synthesis, SAR and molecular modeling studies Synthesis and biological activities of new pyrrolocarbazole-imidazobenzimidazole conjugates Synthesis, protein kinase inhibitory potencies and in vitro antiproliferative activities of meridianin derivatives SYNTHESE ET REACTIVITE D'ALCOOLS ALLYLIQUES A STRUCTURE 1,4-BENZODIOXINIQUE, APPLICATIONS EN SYNTHESE ORGANIQUE Synthesis and kinase inhibitory potencies of new pyrido[3,4-g]quinazolines substituted at the 8-position https://orbi.uliege.be/handle/2268/86605#id From benzofuro-, benzothieno- and 10-methylindolo-[2,3-b]-fused benzothiopyrano[4,3,2-de]quinolines to the corresponding benzothiopyrano[4,3,2-de]1,8-naphthyridines: synthesis and properties of these hexacyclic heteroaromatic compounds
is primary topic of	http://www.idref.fr/142933651
is Opponent of	http://www.sudoc.fr/159177707/id http://www.sudoc.fr/191605921/id http://www.sudoc.fr/203080173/id
is Thesis referee of	http://www.sudoc.fr/175101930/id http://www.sudoc.fr/201225581/id http://www.sudoc.fr/197828604/id http://www.sudoc.fr/166695297/id http://www.sudoc.fr/167312685/id http://www.sudoc.fr/185667368/id http://www.sudoc.fr/258976225/id http://www.sudoc.fr/261259032/id http://www.sudoc.fr/259451037/id http://www.sudoc.fr/233561137/id http://www.sudoc.fr/255980477/id http://www.sudoc.fr/245066667/id http://www.sudoc.fr/260593842/id http://www.sudoc.fr/268407053/id http://www.sudoc.fr/260729167/id http://www.sudoc.fr/258149019/id http://www.sudoc.fr/26454465X/id http://www.sudoc.fr/283559330/id

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