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Design, synthesis and preliminary evaluation of a series of histone deacetylase inhibitors carrying a benzodiazepine ring

European journal of medicinal chemistry, 2013-08, Vol.66, p.56-68

2013

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Trifluoromethyl Fluoroformyl Trioxicarbonate, CF3OC(O)OOOC(O)F: The First Nonsymmetric Acyl Trioxide

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2009-07, Vol.113 (30), p.8523-8528

2009

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Un roman de formation collectif ». Les revues féministes en Italie des années 1970 à nos jours

Laboratoire italien, 2022-07, Vol.28

2022

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Influence of ring size on the cognition-enhancing activity of DM235 and MN19, two potent nootropic drugs

Bioorganic & medicinal chemistry letters, 2012-03, Vol.22 (5), p.1936-1939

2012

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Dynamics of Organochlorine Contaminants in Surface Water and in Myriophyllum aquaticum Plants of the River Xanaes in Central Argentina During the Annual Dry Season

Archives of environmental contamination and toxicology, 2013-10, Vol.65 (3), p.466-473

2013

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HCN Channels Modulators: The Need for Selectivity

Current topics in medicinal chemistry, 2016-07, Vol.16 (16), p.1764-1791

2016

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Structure-affinity relationships of a unique nicotinic ligand: N(1)-dimethyl-N(4)-phenylpiperazinium iodide (DMPP)

Journal of medicinal chemistry, 2001-11, Vol.44 (23), p.3946-3955

2001

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AMPA-receptor activation is involved in the antiamnesic effect of DM 232 (unifiram) and DM 235 (sunifiram)

Naunyn-Schmiedeberg's archives of pharmacology, 2003-12, Vol.368 (6), p.538-545

2003

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Molecular Simplification of 1,4-Diazabicyclo[4.3.0]nonan-9-ones Gives Piperazine Derivatives That Maintain High Nootropic Activity

Journal of medicinal chemistry, 2000-11, Vol.43 (23), p.4499-4507

2000

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Enantioselective synthesis and preliminary pharmacological evaluation of the enantiomers of unifiram (DM232), a potent cognition-enhancing agent

Medicinal chemistry (Shp-sariqah, United Arab Emirates), 2005-09, Vol.1 (5), p.473-480

2005

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Thermal decomposition of trifluoromethoxycarbonyl peroxy nitrate, CF3OC(O)O2NO2

International journal of chemical kinetics, 2008-12, Vol.40 (12), p.831-838

2008

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Structure−Activity Relationships Studies in a Series of N,N-Bis(alkanol)amine Aryl Esters as P-Glycoprotein (Pgp) Dependent Multidrug Resistance (MDR) Inhibitors

Journal of medicinal chemistry, 2010-02, Vol.53 (4), p.1755-1762

2010

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Inhibition of P-glycoprotein-mediated Multidrug Resistance (MDR) by N,N-bis(cyclohexanol)amine aryl esters: Further restriction of molecular flexibility maintains high potency and efficacy

Bioorganic & medicinal chemistry letters, 2011-01, Vol.21 (1), p.106-109

2011

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N,N-bis(Cyclohexanol)amine Aryl Esters: A New Class of Highly Potent Transporter-Dependent Multidrug Resistance Inhibitors

Journal of medicinal chemistry, 2009-02, Vol.52 (3), p.807-817

2009

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Design and study of piracetam-like nootropics, controversial members of the problematic class of cognition-enhancing drugs

Current pharmaceutical design, 2002, Vol.8 (2), p.125-138

2002

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Structure–activity relationships in 2,2-diphenyl-2-ethylthioacetic acid esters: unexpected agonistic activity in a series of muscarinic antagonists

Bioorganic & medicinal chemistry, 2001-05, Vol.9 (5), p.1165-1174

2001

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Exploratory Chemistry toward the Identification of a New Class of Multidrug Resistance Reverters Inspired by Pervilleine and Verapamil Models

Journal of medicinal chemistry, 2005-11, Vol.48 (23), p.7426-7436

2005

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Fish processing wastewater as a platform of the microalgal biorefineries

Biosystems engineering, 2013-06, Vol.115 (2), p.195-202

2013

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Isomeric N,N-Bis(cyclohexanol)amine Aryl Esters: The Discovery of a New Class of Highly Potent P-Glycoprotein (Pgp)-dependent Multidrug Resistance (MDR) Inhibitors

Journal of medicinal chemistry, 2007-02, Vol.50 (4), p.599-602

2007

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Nuclear localization dictates hepatocarcinogenesis suppression by glycine N-methyltransferase

Translational oncology, 2022-01, Vol.15 (1), p.101239-101239, Article 101239

2022

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Highly Chiral Muscarinic Ligands: The Discovery of (2 S ,2‘ R ,3‘ S ,5‘ R )-1-Methyl-2-(2-methyl-1,3-oxathiolan-5-yl)pyrrolidine 3-sulfoxide Methyl Iodide, a Potent, Functionally Selective, M 2 Partial Agonist

Journal of medicinal chemistry, 2006-03, Vol.49 (6), p.1925-1931

2006

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Differential analgesic activity of the enantiomers of atropine derivatives does not correlate with their muscarinic subtype selectivity

European journal of medicinal chemistry, 1997-07, Vol.32 (7), p.595-605

1997

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Trifluoromethyl Fluoroformyl Trioxicarbonate, CF 3 OC(O)OOOC(O)F: The First Nonsymmetric Acyl Trioxide

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2009-07, Vol.113 (30), p.8523-8528

2009

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The medicinal chemistry of Alzheimer's and Alzheimer-like diseases with emphasis on the cholinergic hypothesis

Farmaco (Società chimica italiana : 1989), 1995-07, Vol.50 (7-8), p.489

1995

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Design, Synthesis, and Preliminary Pharmacological Evaluation of a Set of Small Molecules That Directly Activate Gi Proteins

Journal of medicinal chemistry, 2005-10, Vol.48 (20), p.6491-6503

2005

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Design, synthesis and preliminary evaluation of a series of histone deacetylase inhibitors carrying a benzodiazepine ring

Trifluoromethyl Fluoroformyl Trioxicarbonate, CF3OC(O)OOOC(O)F: The First Nonsymmetric Acyl Trioxide

Un roman de formation collectif ». Les revues féministes en Italie des années 1970 à nos jours

Influence of ring size on the cognition-enhancing activity of DM235 and MN19, two potent nootropic drugs

Dynamics of Organochlorine Contaminants in Surface Water and in Myriophyllum aquaticum Plants of the River Xanaes in Central Argentina During the Annual Dry Season

HCN Channels Modulators: The Need for Selectivity

Structure-affinity relationships of a unique nicotinic ligand: N(1)-dimethyl-N(4)-phenylpiperazinium iodide (DMPP)

AMPA-receptor activation is involved in the antiamnesic effect of DM 232 (unifiram) and DM 235 (sunifiram)

Molecular Simplification of 1,4-Diazabicyclo[4.3.0]nonan-9-ones Gives Piperazine Derivatives That Maintain High Nootropic Activity

Enantioselective synthesis and preliminary pharmacological evaluation of the enantiomers of unifiram (DM232), a potent cognition-enhancing agent

Thermal decomposition of trifluoromethoxycarbonyl peroxy nitrate, CF3OC(O)O2NO2

Structure−Activity Relationships Studies in a Series of N,N-Bis(alkanol)amine Aryl Esters as P-Glycoprotein (Pgp) Dependent Multidrug Resistance (MDR) Inhibitors

Inhibition of P-glycoprotein-mediated Multidrug Resistance (MDR) by N,N-bis(cyclohexanol)amine aryl esters: Further restriction of molecular flexibility maintains high potency and efficacy

N,N-bis(Cyclohexanol)amine Aryl Esters: A New Class of Highly Potent Transporter-Dependent Multidrug Resistance Inhibitors

Design and study of piracetam-like nootropics, controversial members of the problematic class of cognition-enhancing drugs

Structure–activity relationships in 2,2-diphenyl-2-ethylthioacetic acid esters: unexpected agonistic activity in a series of muscarinic antagonists

Exploratory Chemistry toward the Identification of a New Class of Multidrug Resistance Reverters Inspired by Pervilleine and Verapamil Models

Fish processing wastewater as a platform of the microalgal biorefineries

Isomeric N,N-Bis(cyclohexanol)amine Aryl Esters: The Discovery of a New Class of Highly Potent P-Glycoprotein (Pgp)-dependent Multidrug Resistance (MDR) Inhibitors

Nuclear localization dictates hepatocarcinogenesis suppression by glycine N-methyltransferase

Highly Chiral Muscarinic Ligands: The Discovery of (2 S ,2‘ R ,3‘ S ,5‘ R )-1-Methyl-2-(2-methyl-1,3-oxathiolan-5-yl)pyrrolidine 3-sulfoxide Methyl Iodide, a Potent, Functionally Selective, M 2 Partial Agonist

Differential analgesic activity of the enantiomers of atropine derivatives does not correlate with their muscarinic subtype selectivity

Trifluoromethyl Fluoroformyl Trioxicarbonate, CF 3 OC(O)OOOC(O)F: The First Nonsymmetric Acyl Trioxide

The medicinal chemistry of Alzheimer's and Alzheimer-like diseases with emphasis on the cholinergic hypothesis

Design, Synthesis, and Preliminary Pharmacological Evaluation of a Set of Small Molecules That Directly Activate Gi Proteins

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