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Hiroki Gunji

Novartis

12

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199

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Structure-based Design of 4-Hydroxy-3,5-Substituted Piperidines as a New Class of Highly Efficacious Oral Direct Renin Inhibitors

2014
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4-Amino-2-cyanopyrimidines: Novel scaffold for nonpeptidic cathepsin S inhibitors

2008 Bioorganic & Medicinal Chemistry Letters
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Overcoming hERG issues for brain-penetrating cathepsin S inhibitors: 2-cyanopyrimidines. Part 2.

2008 Bioorganic & Medicinal Chemistry Letters
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Synthesis and structure-activity relationship of novel RXR antagonists : Orally active anti-diabetic and anti-obesity agents

2007 Bioorganic & Medicinal Chemistry Letters
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Synthesis and structure-activity relationship of RXR antagonists based on the diazepinylbenzoic acid structure.

2007 Bioorganic & Medicinal Chemistry Letters
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Novel scaffold for cathepsin K inhibitors

2007 Bioorganic & Medicinal Chemistry Letters
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Oligonucleosides with a Nucleobase-Including Backbone. Part 3. Synthesis of Acetyleno-Linked Adenosine Dimers.

2001 ChemInform
- Hiroki Gunji
- Andrea Vasella
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Oligonucleosides with a Nucleobase‐Including Backbone, Part 4, A Convergent Synthesis of Ethynediyl‐Linked Adenosine Tetramers

2000 Helvetica Chimica Acta
- Hiroki Gunji
- Andrea Vasella
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Practical Preparation of (Z)-2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetic Acid: A Side-Chain of the Fourth Generation of Cephem Antibiotics

1994 Bulletin of the Chemical Society of Japan
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Citations (9)