Compound Profiler
Assess drug-likeness with Lipinski Ro5, QED score, PAINS structural alerts, and a 6-axis bioavailability radar. Supports single and batch analysis up to 100 compounds.
Example:
CC(=O)Oc1ccccc1C(=O)O (Aspirin)
WARN Borderline
Calculated Properties
MW (g/mol)
408.3
LogP
3.89
TPSA (Ų)
57.61
H-Donors
1
H-Acceptors
4
QED
0.617
Rotatable
3
Fraction Csp3
0.062
Arom. Rings
2
RO5 Violations
0
ESOL Log S
-6.1
Structural Alerts
1 alert(s) found:
- ene_rhod_A(235)
Batch Analysis (up to 100 compounds)
Click to expand
Calculate properties and assess drug-likeness for multiple SMILES at once.