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Development of a practical and sustainable strategy for the synthesis of ST1535 by an iron-catalyzed Kumada cross-coupling reaction

Tetrahedron letters, 2014-02, Vol.55 (7), p.1376-1378

2014

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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.2343-2355

2005

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Effect of Cobalt(II) Oxide and Manganese(IV) Oxide on Sintering of Tin(IV) Oxide

Journal of the American Ceramic Society, 1996-03, Vol.79 (3), p.799-804

1996

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Synthesis and pharmacological activity of a series of dihydro-1H-pyrrolo[1,2-a]imidazole-2,5(3H,6H)-diones, a novel class of potent cognition enhancers

Journal of medicinal chemistry, 1993-12, Vol.36 (26), p.4214-4220

1993

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Utilização de aglomerante alternativo na construção civil – A aplicação da sustentabilidade

Revista Políticas Públicas & Cidades, 2023-01, Vol.12 (2), p.19-34

2023

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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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Portlandite consumption by red ceramic waste due to alkali activation reaction

Ambiente Construído, 2021-01, Vol.21 (1), p.7-21

2021

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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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Discovery of Diaryl Imidazolidin-2-one Derivatives, a Novel Class of Muscarinic M3 Selective Antagonists (Part 2)

Journal of medicinal chemistry, 2007-04, Vol.50 (7), p.1693-1697

2007

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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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Synthesis and Inotropic Activity of 1-(O-Aminoalkyloximes) of Perhydroindene Derivatives as Simplified Digitalis-like Compounds Acting on the Na+,K+-ATPase

Journal of medicinal chemistry, 2002-01, Vol.45 (1), p.189-207

2002

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A general, [1+4] approach to the synthesis of 3(5)-substituted pyrazoles from aldehydes

Tetrahedron letters, 1998-05, Vol.39 (20), p.3287-3290

1998

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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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17β-O-Aminoalkyloximes of 5β-Androstane-3β,14β-diol with Digitalis-like Activity: Synthesis, Cardiotonic Activity, Structure−Activity Relationships, and Molecular Modeling of the Na+,K+-ATPase Receptor

Journal of medicinal chemistry, 2000-06, Vol.43 (12), p.2332-2349

2000

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ADDITIVE MANUFACTURING BY INSTRUMENTED MASS EXTRUSION

Journal of Engineering Research, 2023-11, Vol.3 (40), p.2-12

2023

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Synthesis of Digitoxigenin from 3β-[(tert-Butyldimethylsilyl)oxy]-17α-iodo- 5β-androstan-14β-ol via 17β Stereoselective Free-Radical Introduction of γ-Butyrolactone Moiety

Journal of organic chemistry, 1997-05, Vol.62 (10), p.3402-3404

1997

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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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INFLUENCE OF THE MAXIMUM PASTE THICKNESS AND THE ADDITION OF SUPERPLASTICIZER ON CONCRETE FLOW UNDER VIBRATION

Journal of Engineering Research, 2023-12, Vol.3 (41), p.2-10

2023

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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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Novel fragmentation reactions of bafilomycin A1

Tetrahedron letters, 1997-09, Vol.38 (39), p.6949-6952

1997

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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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ChemInform Abstract: Development of a Practical and Sustainable Strategy for the Synthesis of ST1535 (IV) by an Iron-Catalyzed Kumada Cross-Coupling Reaction

ChemInform, 2014-07, Vol.45 (29), p.no-no

2014

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Synthesis and Quantitative Structure−Activity Relationships of 17β-(Hydrazonomethyl)-5β-androstane-3β,14β-diol Derivatives That Bind to Na+,K+-ATPase Receptor

Journal of medicinal chemistry, 1996-08, Vol.39 (17), p.3385-3393

1996

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Development of a practical and sustainable strategy for the synthesis of ST1535 by an iron-catalyzed Kumada cross-coupling reaction

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

Effect of Cobalt(II) Oxide and Manganese(IV) Oxide on Sintering of Tin(IV) Oxide

Synthesis and pharmacological activity of a series of dihydro-1H-pyrrolo[1,2-a]imidazole-2,5(3H,6H)-diones, a novel class of potent cognition enhancers

Utilização de aglomerante alternativo na construção civil – A aplicação da sustentabilidade

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

Portlandite consumption by red ceramic waste due to alkali activation reaction

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

Discovery of Diaryl Imidazolidin-2-one Derivatives, a Novel Class of Muscarinic M3 Selective Antagonists (Part 2)

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

Synthesis and Inotropic Activity of 1-(O-Aminoalkyloximes) of Perhydroindene Derivatives as Simplified Digitalis-like Compounds Acting on the Na+,K+-ATPase

A general, [1+4] approach to the synthesis of 3(5)-substituted pyrazoles from aldehydes

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

17β-O-Aminoalkyloximes of 5β-Androstane-3β,14β-diol with Digitalis-like Activity: Synthesis, Cardiotonic Activity, Structure−Activity Relationships, and Molecular Modeling of the Na+,K+-ATPase Receptor

ADDITIVE MANUFACTURING BY INSTRUMENTED MASS EXTRUSION

Synthesis of Digitoxigenin from 3β-[(tert-Butyldimethylsilyl)oxy]-17α-iodo- 5β-androstan-14β-ol via 17β Stereoselective Free-Radical Introduction of γ-Butyrolactone Moiety

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

INFLUENCE OF THE MAXIMUM PASTE THICKNESS AND THE ADDITION OF SUPERPLASTICIZER ON CONCRETE FLOW UNDER VIBRATION

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

Novel fragmentation reactions of bafilomycin A1

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

ChemInform Abstract: Development of a Practical and Sustainable Strategy for the Synthesis of ST1535 (IV) by an Iron-Catalyzed Kumada Cross-Coupling Reaction

Synthesis and Quantitative Structure−Activity Relationships of 17β-(Hydrazonomethyl)-5β-androstane-3β,14β-diol Derivatives That Bind to Na+,K+-ATPase Receptor

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