Look at this code:
from rdkit import Chem
mol =
Chem.MolFromSmiles('O=C(O)C2N3C(=O)C(NC(=O)C(c1ccc(O)cc1)NC(=O)C(N)CC(=O)NC)C3SC2(C)C')
Chem.AssignStereochemistry(mol, flagPossibleStereoCenters=True)
[atom.HasProp('_ChiralityPossible') for atom in mol.GetAtoms()]>>> [0,0,0, ... only zeros ...] I believe this compound contains 5 possible stereo centers (picture attached). How can I get them detected by RDKit? Regards, Michał Nowotka
<<attachment: Screen Shot 2014-01-28 at 12.18.43.png>>
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