Use Case
Find hits before you synthesize a single compound.
Traditional hit identification requires screening hundreds of compounds in the lab with limited throughput. DrugSynq computationally ranks 10,000 candidates in 48 hours, delivering a prioritized list of 10–20 molecules worth making.
How It Works
From target structure to ranked molecules in 48 hours.
Target Preparation
Upload crystal structure (PDB) or provide accession number. DrugSynq handles protein preparation: protonation state assignment, missing loop modeling, water molecule placement at key positions.
Library Upload & Docking Pre-filter
Submit molecule library as SMILES or SDF (up to 10,000 compounds per job). High-throughput rigid docking runs in 4–8 hours, reducing to 500 poses for FEP input. Binding site defined interactively.
FEP Binding Affinity Ranking
Top 500 docking poses enter FEP calculations. Relative ΔΔG values are computed across the candidate set using OPLS4 force field. 36–48 hours total compute time on GPU cluster.
ADMET Scoring & Final Rank
All 500 FEP candidates receive 12-property ADMET scores simultaneously. Multi-parameter optimization surfaces the top 10–20 synthesis candidates. Export synthesis queue and presentation-ready report.
Impact
Before and after DrugSynq.
Have a target? Let's build the hit list.
Share your target PDB and molecule library. We'll run a pilot campaign and show you the ranked output before you commit to a subscription.