Now supporting transmembrane & cofactor-bound targets
Discover drug candidates your competitors won’t.
Wide-space generative chemistry + pose-aware SAR — ranked by Boltz-2. Works on prokaryotic & eukaryotic proteins, with or without cofactors.
Explore more, not just optimize
Diversity-first generation avoids mode collapse and local minima.
Trust the numbers
Boltz-2 scores are primary; docking & contacts add interpretable context.
Pose-aware SAR
Clear interaction maps & 3D poses so chemists can act with confidence.
Built for real-world targets
- Prokaryotic & eukaryotic
- Transmembrane proteins
- Cofactor-bound or apo
- Enzymes & receptors
How it works
- 1
Understand the target
Ingest structures & literature to set constraints and encourage novelty.
- 2
Generate diversely
Multiple chemotype families with synthesizability checks and IP-aware hints.
- 3
Score & explain
Boltz-2 ranking + optional docking/contact maps and tidy, pose-aware SAR cards.
Ready to explore your target?
Want a sample report and pricing?