About: Stéphane Bach

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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	Bach, Stéphane (19..-.... ; spécialiste en biologie marine) Bach, Stéphane (19..-.... ; spécialiste en biologie marine) Bach, Stéphane (19..-.... ; spécialiste en biologie marine)
Life Event	http://www.idref.fr/131509802/birth
preferred label	Bach, Stéphane (19..-.... ; spécialiste en biologie marine)
name	Stéphane Bach
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/eng http://lexvo.org/id/iso639-3/fra
Given name	Stéphane
familyName	Bach
has biographical i...tion (Deprecated)	En poste : station biologique de Roscoff (en 2008) Titulaire d'un doctorat en sciences agronomique et ingénierie biologique de la faculté des sciences agronomiques de Gembloux (Université de Liège, Belgique). PostDoc à Roscoff. Depuis 2005 Ingénieur de recherche CNRS. Spécialiste de criblage moléculaire, analyse haut débit des molécules, modulateurs chimique d'enzymes (protéines kinases) et voies cellulaires. Il s'est spécialisé depuis 3 ans dans la chimie des substances naturelles marines molécules marines à visée thérapeutique. Spécialités de recherche : criblage des métabolites planctoniques, chimie de synthèse, cultures de souches marines. Il travaille au Laboratoire de biologie intégrative des modèles marins à la station biologique de Roscoff (CNRS Sorbonne université).Il est régulièrement membre de jurys de thèses ou directeur de thèses. Il est titulaire d'une HDR, habilitation à diriger des recherches
gender	male
ORCID iD	0000-0002-7186-7483
Scopus ID	56133227800
is sameAs of	Bach, Stéphane (19..-.... ; spécialiste en biologie marine) Bach, Stéphane (19..-.... ; spécialiste en biologie marine) Bach, Stéphane (19..-.... ; spécialiste en biologie marine)
is Thesis advisor of	http://www.sudoc.fr/168407434/id http://www.sudoc.fr/131507141/id http://www.sudoc.fr/151875022/id Utilisation de la levure en tant que modèle et outil, de la compréhension de la cytokinèse à l'étude de sélectivité d'une molécule à potentiel thérapeutique http://www.sudoc.fr/247966460/id http://www.sudoc.fr/253410231/id http://www.sudoc.fr/262560119/id http://www.sudoc.fr/247086568/id Valorisation de substances naturelles marines de Nouvelle-Calédonie d'intérêt en traitement anticancéreux http://www.sudoc.fr/225468425/id Recherche de nouveaux agents anticancéreux agissant par inhibition d'interaction protéine/protéine, caractérisation de leurs effets cellulaire http://www.sudoc.fr/276268806/id
is Author of	Structure-based design of novel quinoxaline-2-carboxylic acids and analogues as Pim-1 inhibitors Marine Natural Products from New Caledonia—A Review http://hub.abes.fr/edp/periodical/medsci/2015/volume_31/issue_5/medsci20153105p538/w Thiazolo[5,4- <i>f</i> ]quinoxalines, Oxazolo[5,4- <i>f</i> ]quinoxalines and Pyrazino[ <i>b,e</i> ]isatins: Synthesis from 6-Aminoquinoxalines and Properties Regorafenib analogues and their ferrocenic counterparts: synthesis and biological evaluation La levure modèle et outil… aussi pour la recherche thérapeutique Natural Product Derivatives For Inhibiting Cellular Necroptosis, Ferroptosis And Oxytosis 2-Aminophenones, a common precursor to N-aryl isatins and acridines endowed with bioactivities Synthesis and biological studies of new quinazolines with ether functions in position 2 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 Using budding yeast to screen for anti-prion drugs New Quinoxaline Derivatives as Dual Pim-1/2 Kinase Inhibitors: Design, Synthesis and Biological Evaluation The Franco-Brazilian network on natural products (FB2NP): a new network promoting cooperation and exchanges in natural products research The Anti-Candida albicans Agent 4-AN Inhibits Multiple Protein Kinases Synthesis of N-pyridyl azoles using a deprotometalation-iodolysis-N-arylation sequence and evaluation of their antiproliferative activity in melanoma cells https://hal.archives-ouvertes.fr/hal-02560495#id Neurymenolide A, a Novel Mitotic Spindle Poison from the New Caledonian Rhodophyta Phacelocarpus neurymenioides Synthesis of N-pyridyl azoles using a deprotometalation-iodolysis-N-arylation sequence and evaluation of their antiproliferative activity in melanoma cells Azine and Diazine Functionalization Using 2,2,6,6-Tetramethylpiperidino-Based Lithium–Metal Combinations: Application to the Synthesis of 5,9-Disubstituted Pyrido[3′,2′:4,5]pyrrolo[1,2-c] pyrimidines Microwave-assisted practical synthesis of 4-imino-3-phenyl-3,4-dihydro-1H-chromeno[2,3-d]pyrimidine-2(5H)-thione derivatives and exploration of their biological activities https://hal.archives-ouvertes.fr/hal-03004422#id Conception, synthèse et évaluation de nouveaux inhibiteurs de TgCDPK1 à visée anti-toxoplasmique Identification of a new series of flavopiridol-like structures as kinase inhibitors with high cytotoxic potency https://hal.archives-ouvertes.fr/hal-04013783#id A combined experimental and theoretical study of the thermal [3+2] cycloaddition of carbonyl ylides with activated alkenes Bioactive Metabolites from the Deep Subseafloor Fungus Oidiodendron griseum UBOCC-A-114129 Synthetic Development of New 3-(4-Arylmethylamino)butyl-5-arylidene-rhodanines under Microwave Irradiation and Their Effects on Tumor Cell Lines and against Protein Kinases https://hal.archives-ouvertes.fr/hal-03011380#id https://hal.archives-ouvertes.fr/hal-01697260#id In vitro identification of imidazo[1,2-a]pyrazine-based antileishmanial agents and evaluation of L. major casein kinase 1 inhibition Practical approach to N-benzyl derivatives of 2-amino-8-methoxy-4H-chromene-3-carbonitrile by reductive amination: Exploration of their effects against protein kinases and in silico ADME profiling Oxazolo[5,4-f]quinoxaline-type selective inhibitors of glycogen synthase kinase-3α (GSK-3α): Development and impact on temozolomide treatment of glioblastoma cells Tamoxifen Inhibits CDK5 Kinase Activity by Interacting with p35/p25 and Modulates the Pattern of Tau Phosphorylation. Quinazoline-based VEGFR-2 inhibitors as potential anti-angiogenic agents: A contemporary perspective of SAR and molecular docking studies Discovery of simplified benzazole fragments derived from the marine benzosceptrin B as necroptosis inhibitors involving the receptor interacting protein Kinase-1 https://hal.archives-ouvertes.fr/hal-02906298#id High-Throughput Screening of marine resources Discovery of DB18, a potent inhibitor of CLK kinases with a high selectivity against DYRK1A kinase Fused Systems Based on 2-Aminopyrimidines: Synthesis Combining Deprotolithiation-in situ Zincation with N -Arylation Reactions and Biological Properties Betulin, a Newly Characterized Compound in Acacia auriculiformis Bark, Is a Multi-Target Protein Kinase Inhibitor Développement de nouveaux inhibiteurs de TgCDPK1 à visée anti-toxoplasmique New pyrido[3,4-g]quinazoline derivatives as CLK1 and DYRK1A inhibitors: synthesis, biological evaluation and binding mode analysis Sibiriline, a new small chemical inhibitor of receptor-interacting protein kinase 1, prevents immune-dependent hepatitis Design, biological evaluation and X-ray crystallography of nanomolar multifunctional ligands targeting simultaneously acetylcholinesterase and glycogen synthase kinase-3 Identification of potential cellular targets of aloisine A by affinity chromatography. Kinase inhibitions in pyrido[4,3-h] and [3,4-g]quinazolines: Synthesis, SAR and molecular modeling studies Nigratine as dual inhibitor of necroptosis and ferroptosis regulated cell death From Quinoxaline, Pyrido[2,3-b]pyrazine and Pyrido[3,4-b]pyrazine to Pyrazino-Fused Carbazoles and Carbolines Overexpression of Eimeria tenella Rhoptry Kinase 2 Induces Early Production of Schizonts 6E11, a highly selective inhibitor of Receptor-Interacting Protein Kinase 1, protects cells against cold hypoxia-reoxygenation injury https://hal.archives-ouvertes.fr/hal-01937243#id Synthesis, antileishmanial activity and cytotoxicity of 2,3-diaryl- and 2,3,8-trisubstituted imidazo[1,2-a]pyrazines Development of new highly potent imidazo[1,2-b]pyridazines targeting Toxoplasma gondii calcium-dependent protein kinase 1 Isolation of drugs active against mammalian prions using a yeast-based screening assay https://hal.archives-ouvertes.fr/hal-02389826#id Protein Folding Activity of Ribosomal RNA Is a Selective Target of Two Unrelated Antiprion Drugs Microwave synthesis of new 3-(3-aminopropyl)-5-arylidene-2-thioxo-1,3-thiazolidine-4-ones as potential Ser/Thr protein kinase inhibitors Conception, synthèse et évaluation de nouveaux inhibiteurs de TgCDPK1 à visée anti-toxoplasmique https://hal.archives-ouvertes.fr/hal-03090384#id From simple quinoxalines to potent oxazolo[5,4-f]quinoxaline inhibitors of glycogen-synthase kinase 3 (GSK3) Synthesis and kinase inhibitory potencies of new pyrido[3,4-g]quinazolines substituted at the 8-position Synthesis and evaluation of C3 substituted chalcone‐based derivatives of 7‐azaindole as protein kinase inhibitors Structure Activity Relationship Studies around DB18, a Potent and Selective Inhibitor of CLK Kinases Synthesis of New 2-Phenylamino-4H-chromene-3-carbonitrile Derivatives and Their Effects on Tumor Cell Lines and against Protein Kinases Identification of Novel Compounds Inhibiting the Kinase Activity of the CDK5/p25 Complex via Direct Binding to p25 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 Roscovitine Targets, Protein Kinases and Pyridoxal Kinase Reactivity Under Microwave Irradiation of 2-amino 4H-chromene-3-carbonitrile as tool for the construction of potential bioactive derivatives

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