
Chemoinformatics
QSAR modelling, virtual screening and ligand-based design across million-compound spaces.
- Lead time
- 3–6 wks
- Stack
- RDKit · OEChem
Digital BioPharm is a full-stack contract research partner for pharma & biotech — now resuming operations. Computational chemistry, medicinal chemistry, synthesis, biology and analytics under one roof, reporting to pharma-grade standards.
Send the target and the stage you are at — a scientist, not a salesperson, replies within two business days.

Digital BioPharm is a contract research organisation built for modern drug discovery — a distributed team of chemists, biologists and engineers delivering programmes for pharma, biotech and academic groups. Founded by Dr. Andrey Voronkov in 2010.
See what we doFrom computational hit finding to pre-clinical candidates: oncology, age-related and neurodegenerative disease, epigenetics and protein–ligand interactions — with cloud-scale cheminformatics behind every decision.
See the pipelineTo compress the distance between a disease and its cure — making rigorous, transparent and fast research available to teams of every size, from first hypothesis to the molecule that reaches the clinic.
Start a programmeNine integrated capabilities you can engage individually or as an end-to-end programme. Every line is scoped, timed and reported to pharma-grade standards.

QSAR modelling, virtual screening and ligand-based design across million-compound spaces.

Hit-to-lead optimisation with a clear SAR roadmap and IP-aware design.

Custom synthesis of building blocks, reference compounds and focused libraries.

In vitro assays, ADME profiling and target-engagement readouts.

Structure elucidation, purity control and impurity profiling.

Freedom-to-operate analysis, prior-art search and patent drafting support.

Secure research platforms, pipelines and custom cheminformatics tooling.

Mechanism-of-action visuals and molecular animations for publications & pitches.

Selected delivered programmes — from target to pre-clinical candidate.
Tell us which stage you are at. We scope the work, name a price and a timeline before anything starts.
Active internal and partnered programmes. Each line is a working target, not a slide.
A distributed, cloud-native discovery platform connecting remote research teams to shared computational and wet-lab capacity.
Design and optimisation of selective inhibitors of the TET family demethylases for epigenetic therapy.
Multi-target lead discovery against aggregation and neuroinflammation pathways.
Small-molecule modulators of stem-cell fate for regenerative and oncology applications.
Target identification and hit discovery across senescence and metabolic ageing axes.
Biophysical evaluation, docking and validation of binding events at scale.
Partnered programmes, contract work or a second opinion on someone else’s data — all three are on the table.
We partner where our science is strongest. Bring a target, a hypothesis or a dataset — we'll bring the team.