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Bioorganic & Medicinal Chemistry Letters
|
September 25, 2003
Structure-activity relationships within a series of caspase inhibitors: effect of leaving group modifications
Brett R Ullman, Teresa Aja, Thomas L Deckwerth, et al.
Biorxiv : the Preprint Server for Biology
|
March 10, 2025
Rapaprotin is Activated by an Endopeptidase to Disassemble 26S Proteasome
Hanjing Peng, Zufeng Guo, Wei Li Wang, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 25, 2002
Acyl dipeptides as reversible caspase inhibitors. Part 2: further optimization
Steven D Linton, Donald S Karanewsky, Robert J Ternansky, et al.
Angewandte Chemie (International Ed. in English)
|
September 17, 2025
Rapaprotin, an Endopeptidase-Activated Proteasome Inhibitor that Induces 26S Disassembly
Hanjing Peng, Zufeng Guo, Wei Li Wang, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 21, 2005
Structure-activity relationships within a series of caspase inhibitors. Part 2: Heterocyclic warheads
Brett R Ullman, Teresa Aja, Ning Chen, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 28, 2004
Oxamyl dipeptide caspase inhibitors developed for the treatment of stroke
Steven D Linton, Teresa Aja, Peter R Allegrini, et al.
The New England Journal of Medicine
|
February 8, 2013
Topical paromomycin with or without gentamicin for cutaneous leishmaniasis
Afif Ben Salah, Nathalie Ben Messaoud, Evelyn Guedri, et al.
Journal of Medicinal Chemistry
|
October 28, 2005
First-in-class pan caspase inhibitor developed for the treatment of liver disease
Steven D Linton, Teresa Aja, Robert A Armstrong, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
Bioorganic & Medicinal Chemistry Letters
|
September 25, 2003
Structure-activity relationships within a series of caspase inhibitors: effect of leaving group modifications
Brett R Ullman, Teresa Aja, Thomas L Deckwerth, et al.
Biorxiv : the Preprint Server for Biology
|
March 10, 2025
Rapaprotin is Activated by an Endopeptidase to Disassemble 26S Proteasome
Hanjing Peng, Zufeng Guo, Wei Li Wang, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 25, 2002
Acyl dipeptides as reversible caspase inhibitors. Part 2: further optimization
Steven D Linton, Donald S Karanewsky, Robert J Ternansky, et al.
Angewandte Chemie (International Ed. in English)
|
September 17, 2025
Rapaprotin, an Endopeptidase-Activated Proteasome Inhibitor that Induces 26S Disassembly
Hanjing Peng, Zufeng Guo, Wei Li Wang, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 21, 2005
Structure-activity relationships within a series of caspase inhibitors. Part 2: Heterocyclic warheads
Brett R Ullman, Teresa Aja, Ning Chen, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 28, 2004
Oxamyl dipeptide caspase inhibitors developed for the treatment of stroke
Steven D Linton, Teresa Aja, Peter R Allegrini, et al.
The New England Journal of Medicine
|
February 8, 2013
Topical paromomycin with or without gentamicin for cutaneous leishmaniasis
Afif Ben Salah, Nathalie Ben Messaoud, Evelyn Guedri, et al.
Journal of Medicinal Chemistry
|
October 28, 2005
First-in-class pan caspase inhibitor developed for the treatment of liver disease
Steven D Linton, Teresa Aja, Robert A Armstrong, et al.
Page
of 3