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P-gp transporter and its role in neurodegenerative diseases

Current topics in medicinal chemistry, 2009-02, Vol.9 (2), p.209

2009

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Spirocyclic Benzopyran-Based Derivatives as New Anti-ischemic Activators of Mitochondrial ATP-Sensitive Potassium Channel

Journal of medicinal chemistry, 2008-11, Vol.51 (21), p.6945-6954

2008

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New N-arylsulfonyl- N-alkoxyaminoacetohydroxamic acids as selective inhibitors of gelatinase A (MMP-2)

Bioorganic & medicinal chemistry, 2004-05, Vol.12 (9), p.2441-2450

2004

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Synthesis and AT1 affinity evaluation of benzamidophenyl analogs of known AT1 receptor ligands with similar aromatic skeleton

ARKIVOC, 2008-04, Vol.2008 (2), p.268-286

2008

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Anti-ischemic properties of a new spiro-cyclic benzopyran activator of the cardiac mito-KATP channel

Biochemical pharmacology, 2010-01, Vol.79 (1), p.39-47

2010

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Predictive models, based on classification algorithms, for compounds potentially active as mitochondrial ATP-sensitive potassium channel openers

Bioorganic & medicinal chemistry, 2009-08, Vol.17 (15), p.5565-5571

2009

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Synthesis and biological evaluation of 5-membered spiro heterocycle-benzopyran derivatives against myocardial ischemia

European journal of medicinal chemistry, 2011-03, Vol.46 (3), p.966-973

2011

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New Benzopyran-Based Openers of the Mitochondrial ATP-Sensitive Potassium Channel with Potent Anti-Ischemic Properties

Journal of medicinal chemistry, 2006-12, Vol.49 (26), p.7600-7602

2006

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2-[(3-Methoxyphenylethyl)phenoxy]-Based ABCB1 Inhibitors: Effect of Different Basic Side-Chains on Their Biological Properties

Journal of medicinal chemistry, 2008-12, Vol.51 (23), p.7602-7613

2008

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NO-glibenclamide derivatives: Prototypes of a new class of nitric oxide-releasing anti-diabetic drugs

Bioorganic & medicinal chemistry, 2009-08, Vol.17 (15), p.5426-5432

2009

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New NO-Releasing Pharmacodynamic Hybrids of Losartan and Its Active Metabolite: Design, Synthesis, and Biopharmacological Properties

Journal of medicinal chemistry, 2006-04, Vol.49 (8), p.2628-2639

2006

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Synthesis and Biological Evaluation of (Hetero)Arylmethyloxy- and Arylmethylamine-phenyl Derivatives as Potent P-glycoprotein Modulating Agents

Journal of medicinal chemistry, 2008-03, Vol.51 (5), p.1415-1422

2008

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Sodium N-(Methylsulfonyl)-N-(4-nitro-2-phenoxyphenyl)sulfamate: A Water-Soluble Nimesulide Prodrug for Parenteral Use

Molecular pharmaceutics, 2010-10, Vol.7 (5), p.1871-1876

2010

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Arylmethyloxyphenyl Derivatives: Small Molecules Displaying P-Glycoprotein Inhibition

Journal of medicinal chemistry, 2006-11, Vol.49 (22), p.6607-6613

2006

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Anti-ischemic properties of a new spiro-cyclic benzopyran activator of the cardiac mitoK channel

Biochemical pharmacology, 2009-10, Vol.79 (1)

2009

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NO-Sartans: A New Class of Pharmacodynamic Hybrids as Cardiovascular Drugs

Journal of medicinal chemistry, 2004-11, Vol.47 (23), p.5597-5600

2004

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Evaluation of the NO-releasing properties of NO-donor linkers

Journal of pharmacy and pharmacology, 2008-02, Vol.60 (2), p.189-195

2008

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The [(Methyloxy)imino]methyl Moiety as a Bioisoster of Aryl. A Novel Class of Completely Aliphatic .beta.-Adrenergic Receptor Antagonists

Journal of medicinal chemistry, 1994-05, Vol.37 (10), p.1518-1525

1994

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N- i-Propoxy- N-biphenylsulfonylaminobutylhydroxamic acids as potent and selective inhibitors of MMP-2 and MT1-MMP

Bioorganic & medicinal chemistry letters, 2005-03, Vol.15 (5), p.1321-1326

2005

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A new development of matrix metalloproteinase inhibitors: twin hydroxamic acids as potent inhibitors of MMPs

Bioorganic & medicinal chemistry letters, 2005-05, Vol.15 (9), p.2311-2314

2005

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Synthesis of heteroaromatic analogues of (2-aryl-1-cyclopentenyl-1-alkylidene)-(arylmethyloxy)amine COX-2 inhibitors: effects on the inhibitory activity of the replacement of the cyclopentene central core with pyrazole, thiophene or isoxazole ring

European journal of medicinal chemistry, 2003-02, Vol.38 (2), p.157-168

2003

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Synthesis and Affinity Evaluation for AT1 Receptor of Phenylsalicylaldoxime-Derivatives Structurally Related to Sartans

Heterocycles, 2008-06, Vol.75 (6), p.1467

2008

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Synthesis and 5-HT2A, 5-HT1A and α1-Binding Affinities of 2-[2-Hydroxy-3-(pyridin-3-yl-methyl)amino]-, 2-[2-Hydroxy-3-(2-pyridin-2-yl-ethyl)amino]- and 2-[2-Hydroxy-3-(4-N-methyl-piperazin-1-yl)-amino]propoxybenzaldehyde-O-(substituted) Benzyl Oximes

Archiv der Pharmazie (Weinheim), 2007-03, Vol.340 (3), p.135-139

2007

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Synthesis and 5-HT2A, 5-HT1A and alpha1-binding affinities of 2-[2-Hydroxy-3-(pyridin-3-yl-methyl)amino]-, 2-[2-hydroxy-3-(2-pyridin-2-yl-ethyl)amino]- and 2-[2-hydroxy-3-(4-N-methyl-piperazin-1-yl)-amino]propoxybenzaldehyde-O-(substituted) benzyl oximes

Archiv der Pharmazie (Weinheim), 2007-03, Vol.340 (3), p.135-139

2007

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Synthesis and 5‐HT 2A , 5‐HT 1A and α 1 ‐Binding Affinities of 2‐[2‐Hydroxy‐3‐(pyridin‐3‐yl‐methyl)amino]‐, 2‐[2‐Hydroxy‐3‐(2‐pyridin‐2‐yl‐ethyl)amino]‐ and 2‐[2‐Hydroxy‐3‐(4‐ N ‐methyl‐piperazin‐1‐yl)‐amino]propoxybenzaldehyde‐ O ‐(substituted) Benzyl Oximes

Archiv der Pharmazie (Weinheim), 2007-03, Vol.340 (3), p.135-139

2007

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P-gp transporter and its role in neurodegenerative diseases

Spirocyclic Benzopyran-Based Derivatives as New Anti-ischemic Activators of Mitochondrial ATP-Sensitive Potassium Channel

New N-arylsulfonyl- N-alkoxyaminoacetohydroxamic acids as selective inhibitors of gelatinase A (MMP-2)

Synthesis and AT1 affinity evaluation of benzamidophenyl analogs of known AT1 receptor ligands with similar aromatic skeleton

Anti-ischemic properties of a new spiro-cyclic benzopyran activator of the cardiac mito-KATP channel

Predictive models, based on classification algorithms, for compounds potentially active as mitochondrial ATP-sensitive potassium channel openers

Synthesis and biological evaluation of 5-membered spiro heterocycle-benzopyran derivatives against myocardial ischemia

New Benzopyran-Based Openers of the Mitochondrial ATP-Sensitive Potassium Channel with Potent Anti-Ischemic Properties

2-[(3-Methoxyphenylethyl)phenoxy]-Based ABCB1 Inhibitors: Effect of Different Basic Side-Chains on Their Biological Properties

NO-glibenclamide derivatives: Prototypes of a new class of nitric oxide-releasing anti-diabetic drugs

New NO-Releasing Pharmacodynamic Hybrids of Losartan and Its Active Metabolite: Design, Synthesis, and Biopharmacological Properties

Synthesis and Biological Evaluation of (Hetero)Arylmethyloxy- and Arylmethylamine-phenyl Derivatives as Potent P-glycoprotein Modulating Agents

Sodium N-(Methylsulfonyl)-N-(4-nitro-2-phenoxyphenyl)sulfamate: A Water-Soluble Nimesulide Prodrug for Parenteral Use

Arylmethyloxyphenyl Derivatives: Small Molecules Displaying P-Glycoprotein Inhibition

Anti-ischemic properties of a new spiro-cyclic benzopyran activator of the cardiac mitoK channel

NO-Sartans: A New Class of Pharmacodynamic Hybrids as Cardiovascular Drugs

Evaluation of the NO-releasing properties of NO-donor linkers

The [(Methyloxy)imino]methyl Moiety as a Bioisoster of Aryl. A Novel Class of Completely Aliphatic .beta.-Adrenergic Receptor Antagonists

N- i-Propoxy- N-biphenylsulfonylaminobutylhydroxamic acids as potent and selective inhibitors of MMP-2 and MT1-MMP

A new development of matrix metalloproteinase inhibitors: twin hydroxamic acids as potent inhibitors of MMPs

Synthesis of heteroaromatic analogues of (2-aryl-1-cyclopentenyl-1-alkylidene)-(arylmethyloxy)amine COX-2 inhibitors: effects on the inhibitory activity of the replacement of the cyclopentene central core with pyrazole, thiophene or isoxazole ring

Synthesis and Affinity Evaluation for AT1 Receptor of Phenylsalicylaldoxime-Derivatives Structurally Related to Sartans

Synthesis and 5-HT2A, 5-HT1A and α1-Binding Affinities of 2-[2-Hydroxy-3-(pyridin-3-yl-methyl)amino]-, 2-[2-Hydroxy-3-(2-pyridin-2-yl-ethyl)amino]- and 2-[2-Hydroxy-3-(4-N-methyl-piperazin-1-yl)-amino]propoxybenzaldehyde-O-(substituted) Benzyl Oximes

Synthesis and 5-HT2A, 5-HT1A and alpha1-binding affinities of 2-[2-Hydroxy-3-(pyridin-3-yl-methyl)amino]-, 2-[2-hydroxy-3-(2-pyridin-2-yl-ethyl)amino]- and 2-[2-hydroxy-3-(4-N-methyl-piperazin-1-yl)-amino]propoxybenzaldehyde-O-(substituted) benzyl oximes

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