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Digitalis-like compounds: the discovery of the O-aminoalkyloxime group as a very powerful substitute for the unsaturated gamma-butyrolactone moiety

Current medicinal chemistry, 2005-01, Vol.12 (20), p.2343

2005

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Novel analogues of Istaroxime, a potent inhibitor of Na +,K +-ATPase: Synthesis, structure–activity relationship and 3D-quantitative structure–activity relationship of derivatives at position 6 on the androstane scaffold

Bioorganic & medicinal chemistry, 2010-06, Vol.18 (12), p.4275-4299

2010

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Novel Analogues of Istaroxime, a Potent Inhibitor of Na+,K+-ATPase: Synthesis and Structure−Activity Relationship

Journal of medicinal chemistry, 2008-08, Vol.51 (15), p.4601-4608

2008

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Structure-Based Design and Synthesis of Novel Potent Na+,K+-ATPase Inhibitors Derived from a 5α,14α-Androstane Scaffold as Positive Inotropic Compounds

Journal of medicinal chemistry, 2003-08, Vol.46 (17), p.3644-3654

2003

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17α-O-(Aminoalkyl)oxime Derivatives of 3β,14β-Dihydroxy-5β-androstane and 3β-Hydroxy-14-oxoseco-D-5β-androstane as Inhibitors of Na+,K+-ATPase at the Digitalis Receptor

Journal of medicinal chemistry, 2001-11, Vol.44 (23), p.3821-3830

2001

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Simplified Digitalis-like Compounds acting on Na+, K+-ATPase

Journal of enzyme inhibition and medicinal chemistry, 2003-08, Vol.18 (4), p.289-295

2003

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17β-(3-Furyl)-5β-androstane-3β,14β,17α-triol (PST 2238). A Very Potent Antihypertensive Agent with a Novel Mechanism of Action

Journal of medicinal chemistry, 1997-05, Vol.40 (11), p.1561-1564

1997

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An Expeditious Route to 3β,14β-Dihydroxy-5β-androstane-17β-carboxaldehyde

Synthetic communications, 1997-03, Vol.27 (6), p.1115-1122

1997

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Recent advances in antihypertensive therapy

Current pharmaceutical design, 1998-12, Vol.4 (6), p.489

1998

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A New Approach to the Design of Novel Inhibitors of Na+,K+-ATPase: 17α-Substituted Seco-D 5β-Androstane as Cassaine Analogues

Journal of medicinal chemistry, 1998-07, Vol.41 (16), p.3033-3040

1998

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Structure-based design and synthesis of novel potent Na+,K+ -ATPase inhibitors derived from a 5alpha,14alpha-androstane scaffold as positive inotropic compounds

Journal of medicinal chemistry, 2003-08, Vol.46 (17), p.3644

2003

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Structure-based design and synthesis of novel potent Na+, K+-ATPase inhibitors derived from a 5α14α-androstane scaffold as positive inotropic compounds

Journal of medicinal chemistry, 2003, Vol.46 (17), p.3644-3654

2003

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Digitalis-like compounds: Synthesis and biological evaluation of 3β-(aminoalkylthio) derivatives

Bioorganic & medicinal chemistry letters, 1997-02, Vol.7 (4), p.469-472

1997

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Digitalis-like compounds: Synthesis and biological evaluation of seco-D and D-homo derivatives

Steroids, 1996-10, Vol.61 (10), p.572-582

1996

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Enamines 431. A Simple Synthesis of 4-Amino-4,5-dihydro-1H-imidazoles

Synthesis (Stuttgart), 1983, Vol.1983 (11), p.940-942

1983

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Enamines 43 1 . A Simple Synthesis of 4-Amino-4,5-dihydro-1 H -imidazoles

Synthesis (Stuttgart), 1983, Vol.1983 (11), p.940-942

1983

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ChemInform Abstract: Recent Advances in Antihypertensive Therapy

ChemInform, 1999-02, Vol.30 (5), p.no-no

1999

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Exosomes Recovered From the Plasma of COVID-19 Patients Expose SARS-CoV-2 Spike-Derived Fragments and Contribute to the Adaptive Immune Response

Frontiers in immunology, 2022-01, Vol.12, p.785941-785941

2022

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Anti-Phospholipid Antibodies and Coronavirus Disease 2019: Vaccination Does Not Trigger Early Autoantibody Production in Healthcare Workers

Frontiers in immunology, 2022-07, Vol.13, p.930074-930074

2022

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TMEM123 a key player in immune surveillance of colorectal cancer

Frontiers in immunology, 2023-06, Vol.14, p.1194087-1194087

2023

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Corrigendum: TMEM123 a key player in immune surveillance of colorectal cancer

Frontiers in immunology, 2023-07, Vol.14, p.1256713-1256713

2023

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The Impact of Anti-rheumatic Drugs on the Seroprevalence of Anti-SARS-CoV-2 Antibodies in a Cohort of Patients With Inflammatory Arthritis: The MAINSTREAM Study

Frontiers in medicine, 2022-03, Vol.9, p.850858-850858

2022

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Tracking the immune response profiles elicited by the BNT162b2 vaccine in COVID-19 unexperienced and experienced individuals

Clinical immunology (Orlando, Fla.), 2024-04, Vol.261, p.110164-110164, Article 110164

2024

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Abstract 2829: A novel candidate for immunotherapy mediating the balance between the immune system and cancer

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.2829-2829

2020

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Digitalis-like compounds: the discovery of the O-aminoalkyloxime group as a very powerful substitute for the unsaturated gamma-butyrolactone moiety

Novel analogues of Istaroxime, a potent inhibitor of Na +,K +-ATPase: Synthesis, structure–activity relationship and 3D-quantitative structure–activity relationship of derivatives at position 6 on the androstane scaffold

Novel Analogues of Istaroxime, a Potent Inhibitor of Na+,K+-ATPase: Synthesis and Structure−Activity Relationship

Structure-Based Design and Synthesis of Novel Potent Na+,K+-ATPase Inhibitors Derived from a 5α,14α-Androstane Scaffold as Positive Inotropic Compounds

17α-O-(Aminoalkyl)oxime Derivatives of 3β,14β-Dihydroxy-5β-androstane and 3β-Hydroxy-14-oxoseco-D-5β-androstane as Inhibitors of Na+,K+-ATPase at the Digitalis Receptor

Simplified Digitalis-like Compounds acting on Na+, K+-ATPase

17β-(3-Furyl)-5β-androstane-3β,14β,17α-triol (PST 2238). A Very Potent Antihypertensive Agent with a Novel Mechanism of Action

An Expeditious Route to 3β,14β-Dihydroxy-5β-androstane-17β-carboxaldehyde

Recent advances in antihypertensive therapy

A New Approach to the Design of Novel Inhibitors of Na+,K+-ATPase: 17α-Substituted Seco-D 5β-Androstane as Cassaine Analogues

Structure-based design and synthesis of novel potent Na+,K+ -ATPase inhibitors derived from a 5alpha,14alpha-androstane scaffold as positive inotropic compounds

Structure-based design and synthesis of novel potent Na+, K+-ATPase inhibitors derived from a 5α14α-androstane scaffold as positive inotropic compounds

Digitalis-like compounds: Synthesis and biological evaluation of 3β-(aminoalkylthio) derivatives

Digitalis-like compounds: Synthesis and biological evaluation of seco-D and D-homo derivatives

Enamines 431. A Simple Synthesis of 4-Amino-4,5-dihydro-1H-imidazoles

Enamines 43 1 . A Simple Synthesis of 4-Amino-4,5-dihydro-1 H -imidazoles

ChemInform Abstract: Recent Advances in Antihypertensive Therapy

Exosomes Recovered From the Plasma of COVID-19 Patients Expose SARS-CoV-2 Spike-Derived Fragments and Contribute to the Adaptive Immune Response

Anti-Phospholipid Antibodies and Coronavirus Disease 2019: Vaccination Does Not Trigger Early Autoantibody Production in Healthcare Workers

TMEM123 a key player in immune surveillance of colorectal cancer

Corrigendum: TMEM123 a key player in immune surveillance of colorectal cancer

Immunosuppressant Treatment in Rheumatic Musculoskeletal Diseases Does Not Inhibit Elicitation of Humoral Response to SARS-CoV-2 Infection and Preserves Effector Immune Cell Populations

The Impact of Anti-rheumatic Drugs on the Seroprevalence of Anti-SARS-CoV-2 Antibodies in a Cohort of Patients With Inflammatory Arthritis: The MAINSTREAM Study

Tracking the immune response profiles elicited by the BNT162b2 vaccine in COVID-19 unexperienced and experienced individuals

Abstract 2829: A novel candidate for immunotherapy mediating the balance between the immune system and cancer

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