In one aspect, the invention relates to substituted urea depsipeptide analogs, derivatives thereof, and related compounds, which are useful as activators the ClpP endopeptidease; synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating infectious disease using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
Substituted Urea Depsipeptide Analogs As Activators Of The Clpp Endopeptidase
In one aspect, the invention relates to substituted urea depsipeptide analogs, derivatives thereof, and related compounds, which are useful as activators the ClpP endopeptidease; synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating infectious disease using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
Aryl Substituted Aminomethyl Spectinomycin Analogs As Antibacterial Agents
- Memphis TN, US Samanthi L. Waidyarachchi - Southaven MS, US David F. Bruhn - Memphis TN, US Zhong Zheng - Irvine CA, US Jason W. Rosch - Memphis TN, US
Assignee:
ST. JUDE CHILDREN'S RESEARCH HOSPITAL, INC. - Memphis TN
The invention relates to aryl substituted aminomethyl spectinomycin analogs, derivatives thereof, and related compounds, which are useful as anti-bacterial agents; methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating anti-bacterial infections using the compounds and compositions.
Substituted Urea Depsipeptide Analogs As Activators Of The Clpp Endopeptidase
- Memphis TN, US Ying Zhao - Memphis TN, US Elizabeth Griffith - Germantown TN, US Zhong Zheng - Irvine CA, US Aman P. Singh - Memphis TN, US
International Classification:
C07K 11/02 A61K 45/06 C12N 9/50 A61K 38/15
Abstract:
In one aspect, the invention relates to substituted urea depsipeptide analogs, derivatives thereof, and related compounds, which are useful as activators the ClpP endopeptidease; synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating infectious disease using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.