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)
OK Drug-like
Calculated Properties
MW (g/mol)
243.31
LogP
1.34
TPSA (Ų)
70.91
H-Donors
3
H-Acceptors
2
QED
0.745
Rotatable
2
Fraction Csp3
0.357
Arom. Rings
2
RO5 Violations
0
ESOL Log S
-3.54
Structural Alerts
1 alert(s) found:
- indol_3yl_alk(461)
Batch Analysis (up to 100 compounds)
Click to expand
Calculate properties and assess drug-likeness for multiple SMILES at once.