Search Results - "Montéro, Jean Louis"
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Water-Dispersible Sugar-Coated Iron Oxide Nanoparticles. An Evaluation of their Relaxometric and Magnetic Hyperthermia Properties
Published in Journal of the American Chemical Society (13-07-2011)“…Synthesis of functionalized magnetic nanoparticles (NPs) for biomedical applications represents a current challenge. In this paper we present the synthesis and…”
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Carbonic anhydrase IX: A new druggable target for the design of antitumor agents
Published in Medicinal research reviews (01-05-2008)“…Carbonic anhydrases (CAs, EC 4.2.1.1) are a family of enzymes widespread in all life kingdoms. In mammals, isozyme CA IX is highly overexpressed in many cancer…”
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Therapeutic potential of sulfamides as enzyme inhibitors
Published in Medicinal research reviews (01-11-2006)“…Sulfamide, a quite simple molecule incorporating the sulfonamide functionality, widely used by medicinal chemists for the design of a host of biologically…”
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Sulfamates and their therapeutic potential
Published in Medicinal research reviews (01-03-2005)“…Starting from the very simple molecule sulfamic acid, O‐substituted‐, N‐substituted‐, or di‐/tri‐substituted sulfamates may be obtained, which show specific…”
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Design of zinc binding functions for carbonic anhydrase inhibitors
Published in Current pharmaceutical design (01-03-2008)“…Zinc ion plays a crucial role in the protein's functions and is linked to a variety of physiological processes. It constitutes an essential component of…”
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Antiangiogenic activity of neutral lipids, glycolipids, and phospholipids fractions of Pinus halepensis Mill. seeds
Published in Industrial crops and products (01-03-2014)“…•Lipid fractions (neutral lipids, glycolipids and phospholipids) of Pinus halepensis Mill. seeds were complexed by β-Cyclodextrin.•No cytotoxicity effect was…”
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Analysis of polar lipid fraction of Pinus halepensis Mill. seeds from North Algeria
Published in Industrial crops and products (01-11-2013)“…•Herein, the lipid fraction of Pinus halepensis Mill. seeds has been characterized.•The lipids fractions were separated by LC and the lipids sub fractions were…”
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A Very Efficient Synthesis of a Mannosyl Orthoester [2]Rotaxane and Mannosidic [2]Rotaxanes
Published in Organic letters (06-03-2008)“…The direct preparation of mannosyl[2]rotaxane derivatives by O-glycosylation from tetra-O-acetyl-α-d-mannosyltrichloroacetimidate and a tert-butylanilinium…”
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Inhibition of carbonic anhydrase IX: a new strategy against cancer
Published in Anti-cancer agents in medicinal chemistry (01-07-2009)“…Of the thirteen active carbonic anhydrase (CA) isozymes, the transmembrane isoform CA IX has been shown to be linked with carcinogenesis. CA IX presents an…”
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New zinc binding motifs in the design of selective carbonic anhydrase inhibitors
Published in Mini reviews in medicinal chemistry (01-08-2006)“…The carbonic anhydrases (CAs, EC 4.2.1.1) are ubiquitous zinc enzymes which catalyze a very simple physiological reaction, the interconversion between carbon…”
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BiX3 as an efficient and selective reagent for the halogen exchange reaction
Published in Tetrahedron (12-02-1999)Get full text
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Carbonic anhydrase inhibitors: Copper(II) complexes of polyamino-polycarboxylamido aromatic/heterocyclic sulfonamides are very potent inhibitors of the tumor-associated isoforms IX and XII
Published in Bioorganic & medicinal chemistry (01-01-2008)“…Reaction of EDTA/DTPA dianhydride with aromatic/heterocyclic sulfonamides afforded a series of derivatives incorporating polyaminopolycarboxylate tails and…”
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Regio- and stereospecificity in radical cascade cyclizations of TMS-alcyne containing allyl bromomethyldimethylsilyl ethers
Published in Tetrahedron letters (01-07-1998)“…Tandem radical cyclization of (E) and (Z) TMS-homopropargyl allyl bromomethyl-dimethylsilyl ethers is reported to provide an all- cis substituted…”
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14
Synthesis of Mannose-6-Phosphate Analogues and their Utility as Angiogenesis Regulators
Published in ChemMedChem (04-10-2011)“…Sweet utility: An efficient approach, using a key cyclic sulfate intermediate is reported for the synthesis of mannose‐6‐phosphate (M6P) analogues modified at…”
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Carbonic Anhydrase Inhibitors: Design of Membrane-Impermeant Copper(II) Complexes of DTPA-, DOTA-, and TETA-Tailed Sulfonamides Targeting the Tumor-Associated Transmembrane Isoform IX
Published in ChemMedChem (17-11-2008)“…The synthesis and carbonic anhydrase (CA, EC 4.2.1.1) inhibitory activity of two series of aromatic sulfonamides and their CuII derivatives, incorporating…”
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Targeting of the Brucella suis Virulence Factor Histidinol Dehydrogenase by Histidinol Analogues Results in Inhibition of Intramacrophagic Multiplication of the Pathogen
Published in Antimicrobial Agents and Chemotherapy (01-10-2007)“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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Carbonic Anhydrase Inhibitors: Glycosylsulfanilamides Act as Subnanomolar Inhibitors of the Human Secreted Isoform VI
Published in Chemical biology & drug design (01-12-2009)“…A series of sulfonamides incorporating sugar moieties and the sulfanilamide scaffold have been investigated for their interaction with the secretory isoform of…”
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Metal binding functions in the design of carbonic anhydrase inhibitors
Published in Current topics in medicinal chemistry (01-05-2007)“…The carbonic anhydrases (CAs, EC 4.2.1.1) are zinc containing metalloenzymes which catalyse efficiently the reversible hydration of carbon dioxide to…”
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Carbonic Anhydrase Activators: Gold Nanoparticles Coated with Derivatized Histamine, Histidine, and Carnosine Show Enhanced Activatory Effects on Several Mammalian Isoforms
Published in Journal of medicinal chemistry (10-03-2011)“…Lipoic acid moieties were attached to amine or amino acids showing activating properties against the zinc enzyme carbonic anhydrase (CA, EC 4.2.1.1). The…”
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A new β-carbonic anhydrase from Brucella suis, its cloning, characterization, and inhibition with sulfonamides and sulfamates, leading to impaired pathogen growth
Published in Bioorganic & medicinal chemistry (01-02-2011)“…A β-carbonic anhydrase (CA, EC 4.2.1.1) from the bacterial pathogen Brucella suis, bsCA II, has been cloned, purified, and characterized kinetically. bsCA II…”
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