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Design and Synthesis of Novel Potent Non-Peptide and Orally Active Renin Inhibitors

Acta Crystallographica Section A Foundations of Crystallography

doi 10.1107/s0108767396076313

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August 8, 1996

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International Union of Crystallography (IUCr)

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Design and Synthesis of Novel Potent Non-Peptide and Orally Active Renin Inhibitors

Acta Crystallographica Section A Foundations of Crystallography

doi 10.1107/s0108767396076313

Full Text

Abstract

Date

Authors

Publisher

Related search

Design, Synthesis, and Structure-Activity Relationships of Thieno[2, 3-B]pyridin-4-One Derivatives as a Novel Class of Potent, Orally Active, Non-Peptide Luteinizing Hormone-Releasing Hormone Receptor Antagonists

Design and Synthesis of Novel Hybrid Benzamide–peptide Histone Deacetylase Inhibitors

Synthesis and Pharmacological Characterization of Potent, Selective, and Orally Bioavailable Isoindoline Class Dipeptidyl Peptidase IV Inhibitors

Design, Synthesis, and Evaluation of Diarylpyridines and Diarylanilines as Potent Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors

Arylpiperazinylalkylpyridazinones and Analogues as Potent and Orally Active Antinociceptive Agents: Synthesis and Studies on Mechanism of Action

Design, Synthesis, and Pharmacological Evaluation of Novel NAcylhydrazone Derivatives as Potent Histone Deacetylase 6/8 Dual Inhibitors

Design and Synthesis of Potent Inhibitors of the Malaria Parasite Dihydroorotate Dehydrogenase

Synthesis and Biological Evaluation of Novel Isopropanolamine Derivatives as Non-Peptide Human Immunodeficiency Virus Protease Inhibitors

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