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Publications by Eva R. Barth

Higher Carbon Analogues of 1,4-Dihydropyridines as Potent TGFβ/Smad Inhibitors

European Journal of Inorganic Chemistry

Inorganic Chemistry

2019

English

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Synthesis of Novel 2-Chloro-1,4-Dihydropyridines by Chlorination of 2-Hydroxy-1,4-Dihydropyridines With Phosphorus Oxychloride.

Chemical and Pharmaceutical Bulletin

English

Synthesis and Biological Evaluation of New Piplartine Analogues as Potent Aldose Reductase Inhibitors (ARIs)

European Journal of Medicinal Chemistry

English

Toward Second-Generation Cardiomyogenic and Anti-Cardiofibrotic 1,4-Dihydropyridine-Class TGFβ Inhibitors

English

Synthesis and Biological Evaluation of Cyclopropyl Analogues of Fosmidomycin as Potent P. Falciparum Growth Inhibitors

English

Macrocyclic Carbon Suboxide Oligomers as Potent Inhibitors of the Na,K-ATPase

Annals of the New York Academy of Sciences

Philosophy of Science

2003

English

4-Pyridinio-1,4-Dihydropyridines as Calcium Ion Transport Modulators: Antagonist, Agonist, and Dual Action

Oxidative Medicine and Cellular Longevity

English

Biotin Analogues With Antibacterial Activity Are Potent Inhibitors of Biotin Protein Ligase

ACS Medicinal Chemistry Letters

English

Synthesis, Flow Cytometric Evaluation, and Identification of Highly Potent Dipyridamole Analogues as Equilibrative Nucleoside Transporter 1 Inhibitors

Journal of Medicinal Chemistry

Drug Discovery

Molecular Medicine

2007

English

Nucleobase Modified Adefovir (PMEA) Analogues as Potent and Selective Inhibitors of Adenylate Cyclases From Bordetella Pertussis and Bacillus Anthracis

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Eva R. Barth

Higher Carbon Analogues of 1,4-Dihydropyridines as Potent TGFβ/Smad Inhibitors

Related publications

Synthesis of Novel 2-Chloro-1,4-Dihydropyridines by Chlorination of 2-Hydroxy-1,4-Dihydropyridines With Phosphorus Oxychloride.

Synthesis and Biological Evaluation of New Piplartine Analogues as Potent Aldose Reductase Inhibitors (ARIs)

Toward Second-Generation Cardiomyogenic and Anti-Cardiofibrotic 1,4-Dihydropyridine-Class TGFβ Inhibitors

Synthesis and Biological Evaluation of Cyclopropyl Analogues of Fosmidomycin as Potent P. Falciparum Growth Inhibitors

Macrocyclic Carbon Suboxide Oligomers as Potent Inhibitors of the Na,K-ATPase

4-Pyridinio-1,4-Dihydropyridines as Calcium Ion Transport Modulators: Antagonist, Agonist, and Dual Action

Biotin Analogues With Antibacterial Activity Are Potent Inhibitors of Biotin Protein Ligase

Synthesis, Flow Cytometric Evaluation, and Identification of Highly Potent Dipyridamole Analogues as Equilibrative Nucleoside Transporter 1 Inhibitors

Nucleobase Modified Adefovir (PMEA) Analogues as Potent and Selective Inhibitors of Adenylate Cyclases From Bordetella Pertussis and Bacillus Anthracis