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Use of X-ray Co-crystal Structures and Molecular Modeling To Design Potent and Selective Non-peptide Inhibitors of Cathepsin K
American Chemical Society | 1998| -
Use of X-ray Co-crystal Structures and Molecular Modeling To Design Potent and Selective Non-peptide Inhibitors of Cathepsin K
Online Contents | 1998|Contributors: Yamashita, Dennis S. -
Total synthesis of calicheamicinone: new arrangements for actuation of the reductive cycloaromatization of aglycon congeners
National licenceAmerican Chemical Society | 1991| -
TLR2 MODULATOR COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF
Free accessEuropean Patent Office | 2023| -
TLR2 modulator compounds, pharmaceutical compositions and uses thereof
Free accessEuropean Patent Office | 2024| -
TLR2 MODULATOR COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF
Free accessEuropean Patent Office | 2023| -
TLR2 MODULATOR COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF
Free accessEuropean Patent Office | 2021| -
TLR2 modulator compounds, pharmaceutical compositions and uses thereof
Free accessEuropean Patent Office | 2023| -
TLR2 MODULATOR COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF
Free accessEuropean Patent Office | 2021| -
TLR2 modulator compounds, and pharmaceutical compositions and uses thereof
Free accessEuropean Patent Office | 2023| -
The role of conformational constraint in improved oral bioavailability of cathepsin K inhibitors
British Library Conference Proceedings | 2001| -
Structure and Design of Potent and Selective Cathepsin K Inhibitors
American Chemical Society | 1997| -
Structure Activity Relationships of 5-, 6-, and 7-Methyl-Substituted Azepan-3-one Cathepsin K Inhibitors
American Chemical Society | 2006| -
Structure–Activity Relationships and Discovery of a G Protein Biased μ Opioid Receptor Ligand, [(3-Methoxythiophen-2-yl)methyl]({2-[(9R)-9-(pyridin-2-yl)-6-oxaspiro-[4.5]decan-9-yl]ethyl})amine (TRV130), for the Treatment of Acute Severe Pain
Online Contents | 2013|Contributors: Yamashita, Dennis S. -
Solid-Phase Synthesis of a Combinatorial Array of 1,3-Bis(acylamino)-2-butanones, Inhibitors of the Cysteine Proteases Cathepsins K and L
American Chemical Society | 1999|
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