Using rdkit in a for loop to produce png file, but the same png file is produced each time...

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Why H comes in Smiles for the structure on which H is not present...

RDKit not drawing Chlorin...

ValueError: BitVects must be same length (rdkit)...

How can I interpret the features obtained from Chem.RDKFingerprint(mol)...

ArgumentError: rdkit.Chem.rdMolDescriptors.GetMorganFingerprintAsBitVect(Mol, int)...

Can't convert molecule to fingerprint with rdkit...

How to replace Hydrogen atom with another atom using RDKit?...

How to draw sub-structures of a polycyclic aromatic which shows bond angles correctly?...

How to use sysargv module in vs code?...

Why is this rdkit script not working in visual studio code?...

TypeError: 'NoneType' object is not an iterator Rdkit VS code...

Possible to directly feed SMILE structures stored in a pandas dataframe into RDKit to calculate mole...

How would you convert a large sdf file of chemical compounds into individual files containing molecu...

Why do we have to append path for Rdkit in Google Colab...

RDKit How to change from Fingerprint to Mol or Smiles...

Unable to use RDKit in Jupyter or iPython...

AttributeError: 'Image' object has no attribute 'save'...

IPython.display: how to change width, height and resolution of a displayed image...

RDKit: How to change the atom label fontsize?...

graph theory - connect point in 3D space with other three nearest points (distance based)...

Generating conformers of small ligands but preserving correct aromaticity...

Clean way to select from many options in Python...

How can I set error message if it is not belongs to training datasets?...

How can I determine the number of paraffinic CH3, CH2 and CH groups for any molecule with rdkit in P...

Insert matplotlib images into a pandas dataframe...

RDKit: how to check molecules for exact match?...

Python argument error occurs when running rdkit.Chem.SaltRemover(). (Python argument types did not m...

Output of Graph Convolution in deepchem...