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Quinolizidinyl derivatives of bi- and tricyclic systems as potent inhibitors of acetyl- and butyrylcholinesterase with potential in Alzheimer’s disease

European journal of medicinal chemistry, 2011-06, Vol.46 (6), p.2170-2184

2011

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The hydrogen sulphide‐releasing derivative of diclofenac protects against ischaemia–reperfusion injury in the isolated rabbit heart

British journal of pharmacology, 2008-01, Vol.153 (1), p.100-109

2008

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Dithiolethione compounds inhibit Akt signaling in human breast and lung cancer cells by increasing PP2A activity

Oncogene, 2009-10, Vol.28 (43), p.3837-3846

2009

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Modulation of angiogenesis by dithiolethione‐modified NSAIDs and valproic acid

British journal of pharmacology, 2007-05, Vol.151 (1), p.142-151

2007

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Hydrogen sulphide‐releasing diclofenac derivatives inhibit breast cancer‐induced osteoclastogenesis in vitro and prevent osteolysis ex vivo

British journal of pharmacology, 2012-03, Vol.165 (6), p.1914-1925

2012

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H2S RELEASING ASPIRIN PROTECTS AMYLOID BETA INDUCED CELL TOXICITY IN BV-2 MICROGLIAL CELLS

Neuroscience, 2011-10, Vol.193, p.80-88

2011

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Corrigendum to “H2S releasing aspirin protects amyloid beta induced cell toxicity in BV-2 microglial cells” [Neuroscience 193 (2011) 80–88]

Neuroscience, 2012-09, Vol.221, p.225-225

2012

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New histone deacetylase inhibitors as potential therapeutic tools for advanced prostate carcinoma

Journal of cellular and molecular medicine, 2008-12, Vol.12 (6a), p.2457-2466

2008

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Identification of hydrogen sulfide releasing compounds as novel antiresorptive and antitumour agents

Bone (New York, N.Y.), 2011-01, Vol.48 (1), p.S44-S44

2011

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Targeting the plasmepsin 4 orthologs of Plasmodium sp. with "double drug" inhibitors

Protein and peptide letters, 2008-09, Vol.15 (9), p.868

2008

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4-Aminoquinoline quinolizidinyl- and quinolizidinylalkyl-derivatives with antimalarial activity

Bioorganic & medicinal chemistry, 2005-09, Vol.13 (18), p.5338-5345

2005

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H2 S releasing aspirin protects amyloid beta induced cell toxicity in BV-2 microglial cells

Neuroscience, 2011, Vol.193, p.80-88

2011

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H 2S releasing aspirin protects amyloid beta induced cell toxicity in BV-2 microglial cells

Neuroscience, 2011, Vol.193, p.80-88

2011

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High Antiplasmodial Activity of Novel Plasmepsins I and II Inhibitors

Journal of medicinal chemistry, 2006-12, Vol.49 (25), p.7440-7449

2006

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Preparation and pharmacological activities of homolupinanoyl anilides

Farmaco (Società chimica italiana : 1989), 1995-03, Vol.50 (3), p.153

1995

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Old and new targets for innovative antimalarial compounds: the different strategies of the Italian Malaria Network

Parassitologia, 2008-06, Vol.50 (1-2), p.133

2008

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Synthesis and biological investigations of 2-(tetrahydropyran-2'-yl) and 2-(tetrahydrofuran-2'-yl)benzimidazoles

Farmaco (Società chimica italiana : 1989), 1997-08, Vol.52 (8-9), p.499

1997

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H 2 S‐donating sildenafil (ACS6) inhibits superoxide formation and gp91 phox expression in arterial endothelial cells: role of protein kinases A and G

British journal of pharmacology, 2009-01, Vol.155 (7), p.984-994

2009

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Synthesis and biological investigations of 1-(tetrahydropyran-2'-yl)- and 1-(tetrahydrofuran-2'-yl)benzimidazoles and 1/2-(tetrahydropyran-2'-yl)- and 1/2-(tetrahydrofuran-2'-yl)benzotriazoles

Farmaco (Società chimica italiana : 1989), 1997-08, Vol.52 (8-9), p.509

1997

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Epimerization of Lupinine to Epilupinine and vice versa. Reexamination of the Structures of Lupinal and Epilupinal

Helvetica chimica acta, 2005-02, Vol.88 (2), p.245-251

2005

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Plasmepsin II inhibition and antiplasmodial activity of Primaquine–Statine `double-drugs

Bioorganic & medicinal chemistry letters, 2004-06, Vol.14 (11), p.2931-2934

2004

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1-(Arylalkyl)quinolizidine Derivatives and Thio-Isosteric Analogues as Ligands for Sigma Receptors

Helvetica chimica acta, 2004-03, Vol.87 (3), p.580-591

2004

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Preparation and pharmacological activities of 10-homolupinanoyl-2-R-phenothiazines

Farmaco (Società chimica italiana : 1989), 1994-01, Vol.49 (1), p.5

1994

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H2S‐donating sildenafil (ACS6) inhibits superoxide formation and gp91phox expression in arterial endothelial cells: role of protein kinases A and G

British journal of pharmacology, 2008-12, Vol.155 (7), p.984-994

2008

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Quinolizidinyl derivatives of 5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one as ligands for muscarinic receptors

Bioorganic & medicinal chemistry letters, 1999-10, Vol.9 (20), p.3031-3034

1999

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Quinolizidinyl derivatives of bi- and tricyclic systems as potent inhibitors of acetyl- and butyrylcholinesterase with potential in Alzheimer’s disease

The hydrogen sulphide‐releasing derivative of diclofenac protects against ischaemia–reperfusion injury in the isolated rabbit heart

Dithiolethione compounds inhibit Akt signaling in human breast and lung cancer cells by increasing PP2A activity

Modulation of angiogenesis by dithiolethione‐modified NSAIDs and valproic acid

Hydrogen sulphide‐releasing diclofenac derivatives inhibit breast cancer‐induced osteoclastogenesis in vitro and prevent osteolysis ex vivo

H2S RELEASING ASPIRIN PROTECTS AMYLOID BETA INDUCED CELL TOXICITY IN BV-2 MICROGLIAL CELLS

Corrigendum to “H2S releasing aspirin protects amyloid beta induced cell toxicity in BV-2 microglial cells” [Neuroscience 193 (2011) 80–88]

New histone deacetylase inhibitors as potential therapeutic tools for advanced prostate carcinoma

Identification of hydrogen sulfide releasing compounds as novel antiresorptive and antitumour agents

Targeting the plasmepsin 4 orthologs of Plasmodium sp. with "double drug" inhibitors

4-Aminoquinoline quinolizidinyl- and quinolizidinylalkyl-derivatives with antimalarial activity

H2 S releasing aspirin protects amyloid beta induced cell toxicity in BV-2 microglial cells

H 2S releasing aspirin protects amyloid beta induced cell toxicity in BV-2 microglial cells

High Antiplasmodial Activity of Novel Plasmepsins I and II Inhibitors

Preparation and pharmacological activities of homolupinanoyl anilides

Old and new targets for innovative antimalarial compounds: the different strategies of the Italian Malaria Network

Synthesis and biological investigations of 2-(tetrahydropyran-2'-yl) and 2-(tetrahydrofuran-2'-yl)benzimidazoles

H 2 S‐donating sildenafil (ACS6) inhibits superoxide formation and gp91 phox expression in arterial endothelial cells: role of protein kinases A and G

Synthesis and biological investigations of 1-(tetrahydropyran-2'-yl)- and 1-(tetrahydrofuran-2'-yl)benzimidazoles and 1/2-(tetrahydropyran-2'-yl)- and 1/2-(tetrahydrofuran-2'-yl)benzotriazoles

Epimerization of Lupinine to Epilupinine and vice versa. Reexamination of the Structures of Lupinal and Epilupinal

Plasmepsin II inhibition and antiplasmodial activity of Primaquine–Statine `double-drugs

1-(Arylalkyl)quinolizidine Derivatives and Thio-Isosteric Analogues as Ligands for Sigma Receptors

Preparation and pharmacological activities of 10-homolupinanoyl-2-R-phenothiazines

H2S‐donating sildenafil (ACS6) inhibits superoxide formation and gp91phox expression in arterial endothelial cells: role of protein kinases A and G

Quinolizidinyl derivatives of 5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one as ligands for muscarinic receptors

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