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)
BAD Poor
Calculated Properties
MW (g/mol)
533.72
LogP
6.41
TPSA (Ų)
73.31
H-Donors
3
H-Acceptors
6
QED
0.127
Rotatable
12
Fraction Csp3
0.353
Arom. Rings
5
RO5 Violations
2
ESOL Log S
-10.1
Structural Alerts
1 alert(s) found:
- amino_acridine_A(46)
Batch Analysis (up to 100 compounds)
Click to expand
Calculate properties and assess drug-likeness for multiple SMILES at once.