DNA-Encoded Library (DEL) technology involves a novel affinity selection process that integrates chemistry, biology, bioinformatics and computational chemistry to facilitate a rapid drug discovery process, allowing access to more chemical space with lower cost.
In contrast to high throughput screening, DEL requires a very small amount of target protein and minimum assay development. More importantly, it disrupts the concept of “cost-per-well” and allows testing billions of compounds in one tube.
Why our Library is an Ideal Choice for DEL Screening ?
Library Production Service
- 80+ billion synthetic compounds for diversity
- 100+ selective hot cores for latent druggability of compounds
- 35,000+ commercially source building blocks in stock
- Unique multiple on-DNA reactions to build various chemical bonds
- Flexible library construction to accommodate clients’ needs
- Robust and strict quality to control procedures
We provides a one-stop service from target to hit series. Our extended platform enables overall planning and management of protein production, DEL library production, affinity selection, data analysis, hit validation and structural biology for further optimization.
3 Types of Services Designed for Different Needs
Free access to DEL data sharing
Target confidentiality for academics users | Open source
Unprecedented data release
Target confidentiality for all drug developers | Easy access with reduced risk
One-stop solution customizable
Target exclusivity for all drug developers | Access to unique scaffolds
More than Conventional DEL Screening
Irreversible Covalent Screening
- Specially designed library collection with electrophilic warheads
- Optimized selection method to enhance the signal-to-noise ratio
- Optimized selection procedure to counter charge, RNA/DNA interaction and structural integrity of RNA during DEL screen
- Ligand-based Virtual Screening
- Lead-like Chemical Space
- Cost-effective Compound Acquisition
What screening methods can be chosen in WuXi AppTec HitS?
- Well-established method
- Suits a wide variety of targets
- Screening conditions can be designed to achieve the objective
Covalent library screening
In search of irreversible binders for various targets through permanent linkage.
To identify RNA binding molecules targeting disease-associated RNAs through DEL screening technology.