AI-enabled biomedical research

Engineering the next generation of small-molecule medicines

Talia Research Center unites generative chemistry, machine-learning property prediction and computational genomics to design brain-penetrant therapeutics for diseases with no targeted treatment.

5
Top candidates synthesized
<1 µM
Lead compound potency
3
AI model generations
80+
Inhibitors benchmarked

Research areas

Four programs, one computational core

We pair deep disease biology with AI-driven molecular design across discovery and translational science.

Computational Chemistry

AI Drug Discovery & Molecular Design

Generative chemistry and message-passing neural networks (D-MPNN) design and rank novel candidate analogs, predicting potency and ADMET properties before a single compound is made.

Medicinal Chemistry

Targeted Small-Molecule Therapeutics

Structure-based optimization of STING inhibitors and kinase programs (Nek, CLK2), advancing series with improved selectivity, potency and developability.

Genomics

Computational Genomics & Precision Oncology

Whole-genome and tumor–normal paired analysis — SNP, InDel, SV and CNV calling with somatic variant interpretation — to nominate targets and stratify disease.

Translational Biology

Neuroinflammation & CNS Biology

Brain-penetrant therapeutics for interferonopathies such as AGS, SAVI and neuropsychiatric lupus, with long-term opportunities in neurodegeneration.

The platform

An AI-enabled optimization engine

Every design cycle is closed-loop: models generate, rank and filter candidates, then learn from each round of experimental data.

01

Generative Chemistry & ML

AI-driven generation of candidate analogs and SMILES libraries with predicted target activity.

  • Novel analog generation
  • Structure–activity learning
  • Predicted potency (pIC50)
02

ML Activity & Property Ranking

A ranked, review-ready shortlist scored on activity, CNS/ADME properties and synthetic feasibility.

  • Ranked candidate shortlist
  • CNS / ADME modeling
  • Synthetic feasibility scoring
03

Multi-Parameter Optimization

Simultaneous optimization across the properties that make or break a CNS drug.

  • BBB & toxicity modeling
  • MDR1 / BCRP efflux filtering
  • hERG & off-target risk

How we work

A closed-loop, active-learning cycle

Design–Make–Test–Analyze iterations compound model accuracy with every generation.

Design

Generative models propose novel analogs optimized against multiple objectives.

Synthesize

Top-ranked, synthetically feasible candidates are prioritized and made.

Test

In-cell target engagement, IC50, ADME and CNS-exposure assays measure real activity.

Analyze

Results retrain the models, sharpening the next round of predictions.

Model accuracy across generations

Active learning lifted predictive performance from benchmark to sub-micromolar candidates.

Gen 0 · Initial
R² 0.69
Benchmarked on 80 known inhibitors
Gen 1 · Improved
N = 397
Optimized on the YQ analog series
Gen 2 · Refined
< 1 µM
2 refined candidates below 1 µM potency

Pipeline

Programs in progress

A focused portfolio spanning neuroinflammation, oncology and precision-medicine platforms.

ProgramIndicationModalityStage
TRC-S1 — STING inhibitor seriesNeuroinflammation (AGS, SAVI)Brain-penetrant small molecule
Lead Opt
TRC-NP — NPSLE programNeuropsychiatric lupusSmall molecule
Discovery
TRC-N1 — Nek kinase programOncology (lymphoma)Small-molecule kinase inhibitor
Discovery
TRC-C1 — CLK2 modulatorOncologySmall molecule
Discovery
TRC-G1 — Genomics platformPrecision oncologyWGS variant analytics
Research

Pipeline shown for illustration of research scope; stages reflect internal discovery status.

About

A research center built around computation

Talia Research Center is an independent biomedical research organization advancing AI-native drug discovery. We bring machine learning, medicinal chemistry, structural biology and genomics under one roof to attack diseases that conventional approaches have left behind.

We collaborate with industry and academic partners — including Zermatt Biotech — to translate computational predictions into validated, clinic-ready candidates.

Disease-first

We start from unmet need and rare, genetically-defined disease, then engineer the molecule to fit.

Open collaboration

Shared platforms and partnerships accelerate the path from hypothesis to candidate.

Translational rigor

Every prediction is held to experimental and developability standards before it advances.

Let's advance the science together

Partner with us on target discovery, AI-driven optimization or translational collaboration.

Talia Ge

U.S. Sales Representative