Incorporation of early druggability assessment in the drug discovery process provides a means to prioritize target proteins for high-throughput screening. We present chemical fragment arrays as a method that is capable of determining the druggability of a given target with low protein and compound consumption, enabling rapid decision making during early phases of drug discovery
Introduction in the 1990s of the concept of fragment screening opened up for a new era in drug disco...
This topic explains to us the technique of drug discovery. In this we take a protein sample which un...
To develop more effective therapies to treat human diseases, a better method of finding the biologic...
Fragment screening is the process of identifying relatively simple, often weakly potent
Drug discovery encompasses processes ranging from target selection and validation to the selection o...
Over the past decade, fragment-based drug discovery has developed significantly and has gained incre...
*S Supporting Information ABSTRACT: Analyzing the chemical space coverage in commercial fragment scr...
Most libraries for fragment-based drug discovery are restricted to 1,000-10,000 compounds, but over ...
We introduce a novel strategy to sample the bioactive chemical space, which follows up on hits from ...
This book presents a company-based view of the recent progresses in fragment-based drug discovery (F...
Judging if a protein is able to bind orally available molecules with high affinity, i.e. if a protei...
Fragment-based drug design is an established strategy of finding new drugs. Instead of doing mass sc...
Designed multitarget ligands are a popular approach to generating efficient and safe drugs, and frag...
International audienceHigh-throughput screening assays have become the starting point of many drug d...
The purpose of High Throughput Screening (HTS) in pharmaceutical industry is to identify, as soon as...
Introduction in the 1990s of the concept of fragment screening opened up for a new era in drug disco...
This topic explains to us the technique of drug discovery. In this we take a protein sample which un...
To develop more effective therapies to treat human diseases, a better method of finding the biologic...
Fragment screening is the process of identifying relatively simple, often weakly potent
Drug discovery encompasses processes ranging from target selection and validation to the selection o...
Over the past decade, fragment-based drug discovery has developed significantly and has gained incre...
*S Supporting Information ABSTRACT: Analyzing the chemical space coverage in commercial fragment scr...
Most libraries for fragment-based drug discovery are restricted to 1,000-10,000 compounds, but over ...
We introduce a novel strategy to sample the bioactive chemical space, which follows up on hits from ...
This book presents a company-based view of the recent progresses in fragment-based drug discovery (F...
Judging if a protein is able to bind orally available molecules with high affinity, i.e. if a protei...
Fragment-based drug design is an established strategy of finding new drugs. Instead of doing mass sc...
Designed multitarget ligands are a popular approach to generating efficient and safe drugs, and frag...
International audienceHigh-throughput screening assays have become the starting point of many drug d...
The purpose of High Throughput Screening (HTS) in pharmaceutical industry is to identify, as soon as...
Introduction in the 1990s of the concept of fragment screening opened up for a new era in drug disco...
This topic explains to us the technique of drug discovery. In this we take a protein sample which un...
To develop more effective therapies to treat human diseases, a better method of finding the biologic...