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Use Case

Twelve ADMET properties before you commit to synthesis.

More than half of drug candidates that enter clinical trials fail due to ADMET-related issues. DrugSynq flags hERG blockers, metabolic liabilities, and poor permeability at the design stage — when structural changes are still cheap.

ADMET property visualization showing 12 predicted properties across a panel of lead compounds with risk heatmap

Property Coverage

Comprehensive early risk profiling.

The 12 ADMET properties were selected to cover the main failure modes in clinical development: cardiac safety (hERG), hepatic metabolism (CYP panel, HLM), gastrointestinal absorption (Caco-2, solubility), CNS penetration (BBB, P-gp), and mutagenicity (AMES).

Cardiac Safety
hERG InhibitionIC50 class
Hepatic Metabolism
CYP3A4 Inhibitionbinary
CYP2D6 Inhibitionbinary
Metabolic Stability (HLM)t½ class
GI Absorption
Caco-2 PermeabilityPapp class
Aqueous Solubility (pH 7.4)μg/mL class
Oral Bioavailability (F)% class
Distribution & CNS
Plasma Protein Binding% fu class
BBB Penetrationbinary
P-gp Substratebinary
Safety & Physicochemistry
AMES Mutagenicitybinary
LogP / LogD (pH 7.4)numeric

Risk Visualization

ADMET radar — full risk profile at a glance.

Each compound receives a radar chart covering all 12 properties. The shaded area shows the compound's property profile — deviations from the ideal polygon indicate risk areas. Drag the radar onto a PowerPoint slide for your project meeting or medicinal chemistry team review.

The radar also updates as you iterate — compare lead vs. analog side-by-side to visually track ADMET progress across optimization rounds.

Why It Matters

Catch attrition risks early, not in Phase II.

ADMET-related compound failures in clinical development represent billions in lost investment. The cost-to-fix a metabolic liability drops by orders of magnitude when caught at the design stage versus the IND stage.

58%

Clinical Failure Rate

of clinical-stage compound failures are attributed to ADMET-related issues — pharmacokinetics, toxicity, or safety concerns that were not flagged early enough in optimization.

300×

Cost Multiplier

Addressing a structural liability at the lead design stage costs approximately 300× less than addressing the same liability post-IND when clinical studies must be redesigned.

<1h

ADMET Turnaround

ADMET property prediction for 500 compounds takes under 1 hour on DrugSynq infrastructure. Results are available alongside FEP binding affinity in a unified output report.

Stop finding ADMET problems in the clinic.

Run your current lead series through the DrugSynq ADMET engine. See the risk profile before your next synthesis batch.