Paolo's answer was completely correct, but there's an additional point
that's worth mentioning here.
Hs are often included in query molecules with the intent of restricting
possible valence states of atoms, not because the user is actually
interested in matching Hs. In this case you can use the function
Chem.MergeQueryHs() to remove the H atoms in your query molecule and
add/adjust H count queries on the heavy atoms they are connected to.
Here's how that works in your example:
In [6]: params = Chem.SmilesParserParams()
...: params.removeHs=False
...: query = Chem.MolFromSmiles('c1cn[nH]c(N([H])([H]))1', params)
In [7]: m1 = Chem.MolFromSmiles('c1cn[nH]c1N')
...: m2 = Chem.MolFromSmiles('CNc1ccn[nH]1')
...: m3 = Chem.MolFromSmiles('Nc1ccnn(C)1')
In [8]: m1.HasSubstructMatch(query)
Out[8]: False
In [15]: q2 = Chem.MergeQueryHs(query)
In [16]: m1.HasSubstructMatch(q2)
Out[16]: True
In [17]: m2.HasSubstructMatch(q2)
Out[17]: False
In [18]: m3.HasSubstructMatch(q2)
Out[18]: True
You can see what has happened by calling MolToSmarts:
In [19]: Chem.MolToSmarts(q2)
Out[19]: '[#6]1:[#6]:[#7]:[#7H]:[#6]:1-[#7&!H0&!H1]'
Notice that the N atom now has query features attached to it.
I hope this helps,
-greg
On Tue, Nov 5, 2019 at 7:53 PM Markus Heller <mhel...@admarebio.com> wrote:
> Hi,
>
>
>
> I’m trying to understand how to properly use explicit hydrogens in
> substructure searches. Below is an example. I would like to find all
> molecules that contain my query with hydrogens at the nitrogens, and I
> thought I was on the right track … Why does the first query with the
> explicit H not match m1?
>
>
>
> Thanks
>
> Markus
>
>
>
> <code>
>
> from rdkit import Chem
>
> from rdkit.Chem.Draw import IPythonConsole
>
> from rdkit.Chem import rdDepictor
>
>
>
> rdDepictor.SetPreferCoordGen(True)
>
> IPythonConsole.ipython_useSVG = True
>
>
>
> m1 = Chem.MolFromSmiles('c1cn[nH]c1N')
>
> m2 = Chem.MolFromSmiles('CNc1ccn[nH]1')
>
> m3 = Chem.MolFromSmiles('Nc1ccnn(C)1')
>
>
>
> # do not remove explicit H
>
> params = Chem.SmilesParserParams()
>
> params.removeHs=False
>
>
>
> query = Chem.MolFromSmiles('c1cn[nH]c(N([H])([H]))1', params)
>
>
>
> # first should be True, but all are False
>
> m1.HasSubstructMatch(query)
>
> m2.HasSubstructMatch(query)
>
> m3.HasSubstructMatch(query)
>
>
>
> # rebuild query with explicit H removed, not what I want
>
> query = Chem.MolFromSmiles('c1cn[nH]c(N([H])([H]))1')
>
>
>
> m1.HasSubstructMatch(query)
>
> m2.HasSubstructMatch(query)
>
> m3.HasSubstructMatch(query)
>
>
>
> </code>
>
> --
>
> *Markus Heller, PhD*
>
> Senior Scientist
>
> Direct: 604.827.1122 Main: 604.827.1147
>
>
>
> [image: A027228F]
>
> 2405 Wesbrook Mall, 4th Floor, Vancouver, BC V6T 1Z3
>
>
>
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