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Leverage Bright Chemistry Throughout the Drug Discovery Process
Virtual Screening and AI Models
Virtual Screening and AI Models
Design
Design
Enrich performance of in silico screening engines by integrating with our technology to:
Diversify input of seed structures
Focus your library for a particular protein target class
Screen
Screen
Enhance your virtual screening with:
By integrating our diversity engine with your prioritization system in an iterative fashion
By diversifying hits of each screening cycle
By utilizing fragments and disconnections that are easy to follow-up
DNA Encoded Libraries
DNA Encoded Libraries
Design your DNA Encoded Library
Design your DNA Encoded Library
Leverage our technology to create DELs from relevant, available building blocks.
Reliable logistics
Relevant to your target class
Screen
Screen
Enrich your DEL hits by leveraging our Beyond Substructure search to:
Accelerate off-DNA resynthesis with readily available building blocks
Expand SAR with relevant fragments
Diversify your chemotypes by finding relevant off-the-shelf options among commercial HTS libraries
Screening Libraries
Screening Libraries
Find chemical space across screening collections
Full Structure Diversity Source
Full Structure Diversity Source
Prioritize or design DEL libraries
Design focused DOS campaign
Hit-pick HTS collection
Find alternatives among FBS collection
SAR Expansion
SAR Expansion
Find Alternatives
Find Alternatives
Find commercial options to test SAR hypotheses by using Beyond Substructure search with a bias for similarity.
Explore more chemical space faster
Reduce time and money spent on custom synthesis
Get to faster go/no-go decisions
Diversify SAR Hypothesis
Diversify SAR Hypothesis
Find unexpected connectivity patterns using our Beyond Substructure search with a bias for diversity, enriching each SAR cycle with novel hypotheses.
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