

MedSynth
Spatial, agentic drug discovery — designed in augmented reality, scored by AI, sharpened by federated clinical data.
MedSynth™, in nine slides.
Drug discovery still runs on flat, siloed tools.
2D for a 3D problem
Binding happens in three dimensions. Most design still happens on a flat screen, one molecule at a time.
Disconnected engines
Generation, docking, and free-energy tools live in separate silos that rarely share a scoring view.
Cut off from outcomes
Scoring functions can't safely learn from the clinical and real-world data locked inside hospitals.
One platform from target to candidate — in space.
MedSynth™ builds a 3D representation of a biological target, proposes and re-scores candidate molecules with agentic AI, and lets scientists review the whole design session in augmented reality.
Designed in 3D
Review targets and candidates in AR on visionOS, with a desktop fallback.
Scored by agents
A workflow orchestrates potency, toxicity, and synthesis predictors.
Tuned by reality
Re-weighted by real-world outcomes without moving patient data.
Four stages, one continuous loop.
Represent the target
Build spatial, electrostatic, pharmacophoric, and accessibility features of the binding site.
Propose candidates
A generative or search model proposes therapeutics, conditioned on the indication.
Score, multi-objective
Rank on predicted potency, toxicity and off-target risk, and synthesizability.
Review & modify
Scientists edit candidates in AR or 2D; edits are re-scored and fed back into the loop.
Stand inside the binding site.
Render the target and candidate molecules together in three dimensions, positioned in the pocket — then reach in and modify them.
- Apple Vision Pro, running visionOS
- 2D desktop fallback on macOS, Windows, and iPadOS
- Human-in-the-loop edits, re-scored on the spot
visionOS · binding-site viewAn agent runs the bench work.
A workflow manager orchestrates the calls a medicinal chemist would make by hand — and searches the design space far faster.
- Potency, toxicity, and synthesis-difficulty predictors
- Specialized scores: β-lactamase resistance, kinase off-target, cardiotoxicity, IP novelty
- Monte Carlo tree search and RL policies over structural edits
Learn from the clinic. Move no records.
Remote data custodians compute model updates on clinical, omics, and real-world data that never leave their walls. MedSynth™ aggregates the updates — never the patient records.
Data never moves
Hospitals keep patient-level records; only aggregated model updates are shared.
Scored by outcomes
Toxicity, efficacy, resistance, and stratification scores tuned to real-world signals.
Built to govern
A federation service distributes parameters and aggregates gradients, by design.
Plugs into the engines labs already run.
Ingest externally generated candidate sets, then re-rank them with MedSynth's multi-objective scoring and federated weighting. No rip-and-replace.
Docking · FEP · virtual screening
One platform, conditioned per modality.
The moat is the combination.
A small senior team that ships.
Larynx™ is deliberately small. Two people who have built and shipped real systems own every engagement directly — strategy, architecture, and the code itself.
