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Water-Dispersible Sugar-Coated Iron Oxide Nanoparticles. An Evaluation of their Relaxometric and Magnetic Hyperthermia Properties

Journal of the American Chemical Society, 2011-07, Vol.133 (27), p.10459-10472

2011

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Carbonic anhydrase IX: A new druggable target for the design of antitumor agents

Medicinal research reviews, 2008-05, Vol.28 (3), p.445-463

2008

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Therapeutic potential of sulfamides as enzyme inhibitors

Medicinal research reviews, 2006-11, Vol.26 (6), p.767-792

2006

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Sulfamates and their therapeutic potential

Medicinal research reviews, 2005-03, Vol.25 (2), p.186-228

2005

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Antiangiogenic activity of neutral lipids, glycolipids, and phospholipids fractions of Pinus halepensis Mill. seeds

Industrial crops and products, 2014-03, Vol.54, p.6-12

2014

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Analysis of polar lipid fraction of Pinus halepensis Mill. seeds from North Algeria

Industrial crops and products, 2013-11, Vol.51, p.116-122

2013

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A Very Efficient Synthesis of a Mannosyl Orthoester [2]Rotaxane and Mannosidic [2]Rotaxanes

Organic letters, 2008-03, Vol.10 (5), p.753-756

2008

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New zinc binding motifs in the design of selective carbonic anhydrase inhibitors

Mini reviews in medicinal chemistry, 2006-08, Vol.6 (8), p.921

2006

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Inhibition of carbonic anhydrase IX: a new strategy against cancer

Anti-cancer agents in medicinal chemistry, 2009-07, Vol.9 (6), p.693

2009

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Synthesis of Mannose-6-Phosphate Analogues and their Utility as Angiogenesis Regulators

ChemMedChem, 2011-10, Vol.6 (10), p.1771-1774

2011

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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

Bioorganic & medicinal chemistry, 2008-01, Vol.18 (2), p.836-841

2008

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Entropy-driven lectin-recognition of multivalent glycovesicles

Chemical communications (Cambridge, England), 2014-01, Vol.50 (6), p.731-733

2014

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Carbonic Anhydrase Activators: Gold Nanoparticles Coated with Derivatized Histamine, Histidine, and Carnosine Show Enhanced Activatory Effects on Several Mammalian Isoforms

Journal of medicinal chemistry, 2011-03, Vol.54 (5), p.1170-1177

2011

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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

ChemMedChem, 2008-11, Vol.3 (11), p.1780-1788

2008

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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

Antimicrobial Agents and Chemotherapy, 2007-10, Vol.51 (10), p.3752-3755

2007

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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

Bioorganic & medicinal chemistry, 2011-02, Vol.19 (3), p.1172-1178

2011

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Carbonic Anhydrase Inhibitors: Clash with Ala65 as a Means for Designing Inhibitors with Low Affinity for the Ubiquitous Isozyme II, Exemplified by the Crystal Structure of the Topiramate Sulfamide Analogue

Journal of medicinal chemistry, 2006-11, Vol.49 (24), p.7024-7031

2006

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Straightforward synthesis towards mono and bis-phosphonic acid functionalised β-cyclodextrins

Tetrahedron, 2015-03, Vol.71 (10), p.1616-1621

2015

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Carbonic Anhydrase Inhibitors. Design of Fluorescent Sulfonamides as Probes of Tumor-Associated Carbonic Anhydrase IX That Inhibit Isozyme IX-Mediated Acidification of Hypoxic Tumors

Journal of medicinal chemistry, 2005-07, Vol.48 (15), p.4834-4841

2005

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Carbonic Anhydrase Inhibitors: Glycosylsulfanilamides Act as Subnanomolar Inhibitors of the Human Secreted Isoform VI

Chemical biology & drug design, 2009-12, Vol.74 (6), p.636-639

2009

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Metal binding functions in the design of carbonic anhydrase inhibitors

Current topics in medicinal chemistry, 2007-05, Vol.7 (9), p.835

2007

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Mono- and di-halogenated histamine, histidine and carnosine derivatives are potent carbonic anhydrase I, II, VII, XII and XIV activators

Bioorganic & medicinal chemistry, 2014-09, Vol.22 (17), p.4752-4758

2014

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Carbonic Anhydrase Inhibitors: Hypoxia-Activatable Sulfonamides Incorporating Disulfide Bonds that Target the Tumor-Associated Isoform IX

Journal of medicinal chemistry, 2006-09, Vol.49 (18), p.5544-5551

2006

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Thiol-ene click chemistry for the synthesis of highly effective glycosyl sulfonamide carbonic anhydrase inhibitors

Chemical communications (Cambridge, England), 2013-01, Vol.49 (50), p.5699-5701

2013

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Carbonic anhydrase inhibitors: Novel sulfonamides incorporating 1,3,5-triazine moieties as inhibitors of the cytosolic and tumour-associated carbonic anhydrase isozymes I, II and IX

Bioorganic & medicinal chemistry letters, 2005-06, Vol.15 (12), p.3102-3108

2005

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Water-Dispersible Sugar-Coated Iron Oxide Nanoparticles. An Evaluation of their Relaxometric and Magnetic Hyperthermia Properties

Carbonic anhydrase IX: A new druggable target for the design of antitumor agents

Therapeutic potential of sulfamides as enzyme inhibitors

Sulfamates and their therapeutic potential

Antiangiogenic activity of neutral lipids, glycolipids, and phospholipids fractions of Pinus halepensis Mill. seeds

Analysis of polar lipid fraction of Pinus halepensis Mill. seeds from North Algeria

A Very Efficient Synthesis of a Mannosyl Orthoester [2]Rotaxane and Mannosidic [2]Rotaxanes

New zinc binding motifs in the design of selective carbonic anhydrase inhibitors

Inhibition of carbonic anhydrase IX: a new strategy against cancer

Synthesis of Mannose-6-Phosphate Analogues and their Utility as Angiogenesis Regulators

Carbonic anhydrase inhibitors: Copper(II) complexes of polyamino-polycarboxylamido aromatic/heterocyclic sulfonamides are very potent inhibitors of the tumor-associated isoforms IX and XII

Entropy-driven lectin-recognition of multivalent glycovesicles

Carbonic Anhydrase Activators: Gold Nanoparticles Coated with Derivatized Histamine, Histidine, and Carnosine Show Enhanced Activatory Effects on Several Mammalian Isoforms

Carbonic Anhydrase Inhibitors: Design of Membrane-Impermeant Copper(II) Complexes of DTPA-, DOTA-, and TETA-Tailed Sulfonamides Targeting the Tumor-Associated Transmembrane Isoform IX

Targeting of the Brucella suis Virulence Factor Histidinol Dehydrogenase by Histidinol Analogues Results in Inhibition of Intramacrophagic Multiplication of the Pathogen

A new β-carbonic anhydrase from Brucella suis, its cloning, characterization, and inhibition with sulfonamides and sulfamates, leading to impaired pathogen growth

Carbonic Anhydrase Inhibitors: Clash with Ala65 as a Means for Designing Inhibitors with Low Affinity for the Ubiquitous Isozyme II, Exemplified by the Crystal Structure of the Topiramate Sulfamide Analogue

Straightforward synthesis towards mono and bis-phosphonic acid functionalised β-cyclodextrins

Carbonic Anhydrase Inhibitors. Design of Fluorescent Sulfonamides as Probes of Tumor-Associated Carbonic Anhydrase IX That Inhibit Isozyme IX-Mediated Acidification of Hypoxic Tumors

Carbonic Anhydrase Inhibitors: Glycosylsulfanilamides Act as Subnanomolar Inhibitors of the Human Secreted Isoform VI

Metal binding functions in the design of carbonic anhydrase inhibitors

Mono- and di-halogenated histamine, histidine and carnosine derivatives are potent carbonic anhydrase I, II, VII, XII and XIV activators

Carbonic Anhydrase Inhibitors: Hypoxia-Activatable Sulfonamides Incorporating Disulfide Bonds that Target the Tumor-Associated Isoform IX

Thiol-ene click chemistry for the synthesis of highly effective glycosyl sulfonamide carbonic anhydrase inhibitors

Carbonic anhydrase inhibitors: Novel sulfonamides incorporating 1,3,5-triazine moieties as inhibitors of the cytosolic and tumour-associated carbonic anhydrase isozymes I, II and IX

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