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)
478.56
LogP
4.18
TPSA (Ų)
111.76
H-Donors
2
H-Acceptors
7
QED
0.383
Rotatable
7
Fraction Csp3
0.222
Arom. Rings
4
RO5 Violations
0
ESOL Log S
-7.94
Structural Alerts
1 alert(s) found:
- anil_di_alk_A(478)
Batch Analysis (up to 100 compounds)
Click to expand
Calculate properties and assess drug-likeness for multiple SMILES at once.