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Identification of Quaternary Ammonium Compounds as Potent Inhibitors of hERG Potassium Channels

Toxicology and Applied Pharmacology

Toxicology

Pharmacology

2011

English

Discovery of Benzoylsulfonohydrazides as Potent Inhibitors of the Histone Acetyltransferase KAT6A

English

Isoquinoline-Based Analogs of the Cancer Drug Clinical Candidate Tipifarnib as Anti-Trypanosoma Cruzi Agents

Bioorganic and Medicinal Chemistry Letters

Clinical Biochemistry

Pharmaceutical Science

Drug Discovery

2009

English

Studies on 2-Amio-4 or 5-Aryl Substituted Thiazoles. II. On the Ultraviolet Absorption Spectra of Α-Naphthyl, Biphenyl and Hydroxyaryl Substituted Compounds.

Nippon kagaku zassi

1959

English

HMGA2 as a Functional Antagonist of PARP1 Inhibitors in Tumor Cells

English

Synthesis of Poly(lactic Acid) by Direct Polycondensation of Lactic Acid Using 1,1′-Carbonyldiimidazole, N,n,n′,n′-Tetramethylchloroformamidinium Chloride, and N,n′-Dicyclohexylcarbodiimide as Condensing Agents

English

Side Reaction of Significance in Preparation of Peptide- Or Peptidomimetic-Based Hydroxamate Enzyme Inhibitors

English

Structure-Based Design of Submicromolar, Biologically Active Inhibitors of Trypanosomatid Glyceraldehyde-3-Phosphate Dehydrogenase

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

1999

English

Antirhinovirus Activity of Purine Nucleoside Analogs.

Antimicrobial Agents and Chemotherapy

Infectious Diseases

Pharmacology

1986

English

Enantioselective Synthesis of 3-Substituted Isoindolinones via Chiral Phase-Transfer Catalyzed Intramolecular Aza-Michael Reactions

2013

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Identification of Quaternary Ammonium Compounds as Potent Inhibitors of hERG Potassium Channels

Discovery of Benzoylsulfonohydrazides as Potent Inhibitors of the Histone Acetyltransferase KAT6A

Isoquinoline-Based Analogs of the Cancer Drug Clinical Candidate Tipifarnib as Anti-Trypanosoma Cruzi Agents

Studies on 2-Amio-4 or 5-Aryl Substituted Thiazoles. II. On the Ultraviolet Absorption Spectra of Α-Naphthyl, Biphenyl and Hydroxyaryl Substituted Compounds.

HMGA2 as a Functional Antagonist of PARP1 Inhibitors in Tumor Cells

Synthesis of Poly(lactic Acid) by Direct Polycondensation of Lactic Acid Using 1,1′-Carbonyldiimidazole, N,n,n′,n′-Tetramethylchloroformamidinium Chloride, and N,n′-Dicyclohexylcarbodiimide as Condensing Agents

Side Reaction of Significance in Preparation of Peptide- Or Peptidomimetic-Based Hydroxamate Enzyme Inhibitors

Structure-Based Design of Submicromolar, Biologically Active Inhibitors of Trypanosomatid Glyceraldehyde-3-Phosphate Dehydrogenase

Antirhinovirus Activity of Purine Nucleoside Analogs.

Enantioselective Synthesis of 3-Substituted Isoindolinones via Chiral Phase-Transfer Catalyzed Intramolecular Aza-Michael Reactions