Design. Make. Test.
Learn Faster.
SMS Peptides combines computational design, display technologies, and peptide chemistry to identify and prioritize promising peptide hits.
Explore DiscoveryMove from Target to Validated Hit.
An integrated discovery workflow connecting computational design, display technologies, peptide synthesis, and early validation.
Computational Design
Prioritize focused peptide libraries using target information and computational analysis.
Display Technologies
Use phage display and mRNA display approaches to identify target-specific binders.
Hit Confirmation
Synthesize and characterize selected sequences to support early screening and hit-to-lead decisions.
Program Progression
Connect discovery outputs with synthesis, analytical, and pre-clinical development support.
AI + Display Technologies
Our integrated platform combines AI-driven virtual screening with experimental display technologies and automated synthesis to move from target biology to validated peptide hits faster.
Target Selection
Structural Target Profiling
Virtual Screening
AI In-Silico Library Design
Display Selection
Phage & mRNA Display Panning
Hit Identification
Automated Parallel Synthesis
Validation
Biochemical & Cellular Profiling
Target Selection
Analyze target biology, active binding pockets, and conformational states to prioritize druggable peptide epitopes.
- In silico pocket topology & binding cleft analysis
- Structural alignment against known peptide complexes
- Druggability scoring & physicochemical profiling
Ready to Accelerate Your Peptide Pipeline?
Discuss target specifications, display library options, and custom analytical screening with our scientific discovery team.