Creating first-in-class medications to treat human disease is an extremely challenging endeavor. While genome sequencing and genetics are making direct connections between mutations and human disorders at an unprecedented rate, matching molecular targets with a suitable therapeutic indication must ultimately be achieved by pharmacology. Here, we discuss how the integration of chemical proteomic platforms (such as activity-based protein profiling) into the earliest stages of the drug discovery process has the potential to greatly expand the scope of proteins that can be pharmacologically evaluated in living systems, and, through doing so, promote the identification and prioritization of new therapeutic targets
The biomedical and pharmaceutical communities are experiencing a growing demand for new druggable ta...
Genomics represents a new tool in drug discovery. Microbial genomics have been at the forefront of a...
The Undruggable Proteome – those proteins which do not have a canonical small molecule binding pocke...
While many disease-modifying protein targets have been discovered, most of these targets have remain...
AbstractIn drug discovery, chemical screening is performed after a protein's function has been deter...
Preclinical stages in the drug discovery process require a multitude of biochemical and genetic assa...
The emerging field of chemo- and pharmacoproteomics studies the mechanisms of action of bioactive m...
Though many proteins have been identified as relevant to cancer pathogenicity, very few are now targ...
Medical community and pharmaceutical companies are currently facing a dire need for discovery and id...
Despite the completion of human genome sequencing efforts nearly 15 years ago that brought with it t...
A large proportion of biomedical research and the development of therapeutics is focused on a small ...
This thesis submitted in partial fulfillment of the requirements for the degree of Masters of Pharma...
One of the foremost limitations of drug development efforts is that the majority of disease-driving ...
SummaryA chemoproteomics-based drug discovery strategy is presented that utilizes a highly parallel ...
Proteomics is a new enabling technology that is being integrated into the drug discovery process. Th...
The biomedical and pharmaceutical communities are experiencing a growing demand for new druggable ta...
Genomics represents a new tool in drug discovery. Microbial genomics have been at the forefront of a...
The Undruggable Proteome – those proteins which do not have a canonical small molecule binding pocke...
While many disease-modifying protein targets have been discovered, most of these targets have remain...
AbstractIn drug discovery, chemical screening is performed after a protein's function has been deter...
Preclinical stages in the drug discovery process require a multitude of biochemical and genetic assa...
The emerging field of chemo- and pharmacoproteomics studies the mechanisms of action of bioactive m...
Though many proteins have been identified as relevant to cancer pathogenicity, very few are now targ...
Medical community and pharmaceutical companies are currently facing a dire need for discovery and id...
Despite the completion of human genome sequencing efforts nearly 15 years ago that brought with it t...
A large proportion of biomedical research and the development of therapeutics is focused on a small ...
This thesis submitted in partial fulfillment of the requirements for the degree of Masters of Pharma...
One of the foremost limitations of drug development efforts is that the majority of disease-driving ...
SummaryA chemoproteomics-based drug discovery strategy is presented that utilizes a highly parallel ...
Proteomics is a new enabling technology that is being integrated into the drug discovery process. Th...
The biomedical and pharmaceutical communities are experiencing a growing demand for new druggable ta...
Genomics represents a new tool in drug discovery. Microbial genomics have been at the forefront of a...
The Undruggable Proteome – those proteins which do not have a canonical small molecule binding pocke...