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Harry Cheung
Institutions:
Novartis (Switzerland),
Novartis (United States)
Observed institutions:
Novartis (Switzerland),
Novartis (United States),
Elan Pharmaceuticals, Inc. (Ireland)
OpenAlex ID:
A5044044762
Design and Synthesis of Tri-Ring P3 Benzamide-Containing Aminonitriles as Potent, Selective, Orally Effective Inhibitors of Cathepsin K
2005
·
James T. Palmer
, Clifford Bryant
, et al.
·
Journal of Medicinal Chemistry
·
95
Keto-1,3,4-oxadiazoles as cathepsin K inhibitors
2006
·
James T. Palmer
, Bernard L. Hirschbein
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
73
Peptide Ketobenzoxazole Inhibitors Bound to Cathepsin K
2003
·
Mary E. McGrath
, Paul A. Sprengeler
, et al.
·
Biochemistry
·
41
3,4-Disubstituted azetidinones as selective inhibitors of the cysteine protease cathepsin K. Exploring P3 elements for potency and selectivity
2005
·
Eduardo L. Setti
, Dana Davis
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
29
Design and synthesis of tetracyclic nonpeptidic biaryl nitrile inhibitors of cathepsin K
2006
·
Eduardo L. Setti
, Shankar Venkatraman
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
9
Development of a Novel β-Secretase Binding Assay Using the AlphaScreen Platform
2013
·
Zhao Ren
, Danny Tam
, et al.
·
SLAS DISCOVERY
·
7
Discovery of IID432 for Chagas Disease: A Cyanotriazole Inhibitor of Trypanosoma cruzi Topoisomerase II Achieves Sterile Cure After Short-Term Treatment in a Chronic Infection Model
2026
·
Olivier René
, Manuel Saldivia
, et al.
·
Journal of Medicinal Chemistry
·
2
Keto‐1,3,4‐oxadiazoles as Cathepsin K Inhibitors.
2006
·
James T. Palmer
, Bernard L. Hirschbein
, et al.
·
ChemInform
·
1
Discovery of a Pyrazine-2-Carboxamide Derivative as a Potent Plasmodium falciparum Inhibitor with Potential for Single-Dose Cure
2026
·
Vanessa M. Marx
, Anne-Catherine Mata
, et al.
·
Journal of Medicinal Chemistry
Design and Synthesis of Tetracyclic Nonpeptidic Biaryl Nitrile Inhibitors of Cathepsin K.
2006
·
Eduardo L. Setti
, Shankar Venkatraman
, et al.
·
ChemInform
3,4‐Disubstituted Azetidinones as Selective Inhibitors of the Cysteine Protease Cathepsin K. Exploring P3 Elements for Potency and Selectivity.
2005
·
Eduardo L. Setti
, Dana Davis
, et al.
·
ChemInform
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Works count:
11
Citation count:
257
H-index:
6
I10-index:
4
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