Yeah, it would be great if you could create an issue for the general
problem that removeHs() should not remove H atoms that are contributing to
the definition of a stereo bond

On Fri, 6 Apr 2018 at 18:49, Dan Nealschneider <
dan.nealschnei...@schrodinger.com> wrote:

> Thanks, Greg-
>
>
>>
>>> What is the correct treatment of bond stereochemistry at centers for
>>> which a hydrogen is required in order to specify the bond stereochemistry?
>>> For example, an imine with a hydrogen substituent (trivial example,
>>> F/C=N/[H]).
>>>
>>
>> In these cases the H cannot be implicit. The double bond stereochemistry
>> is always defined relative to atoms bonded to the double-bonded atoms (more
>> complex to write than it actually is) and there’s just no way to do this if
>> either of those atoms is implicit.
>>
>
> Ok. It sounds like the correct treatment for my schrodinger/rdkit
> translation layer is to leave these hydrogens explicit.
>
>
>> I notice that when I use the smiles constructor, or if I read from an SDF
>>> file using the SDMolSupplier, the C=N bond in the example shown above is
>>> not recognized as having stereochemistry. However, if I use
>>> removeHydrogens=False in the SDMolSupplier, the bond *is* recognized as
>>> Z.
>>>
>>
>> I need to confirm it (I’m on my phone at the moment), but I think this is
>> a bug: removeHs() should not remove atoms that determine stereochemistry.
>> This might be something I can get fixed before the next release.
>>
>
> Reading from SMILES in RDKit also loses this hydrogen:
>
> Python 3.6.2 (default, Sep 26 2017, 17:33:28)
> [GCC 4.2.1 Compatible Apple LLVM 6.0 (clang-600.0.57)] on darwin
> >>> import rdkit.Chem
> >>> rdkit.__version__
> '2017.03.1'
> >>> m = rdkit.Chem.MolFromSmiles('F/C=N/[H]')
> >>> rdkit.Chem.MolToSmiles(m, isomericSmiles=True)
> 'N=CF'
>
> Would it be useful for me to file a bug report?
>
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