Hi,

My first question  was about identical inputs giving
different 2D coordinate sets, depending on... on what?
On a call to a random number generator?

In a bridged polycyclic system, there is more
than one way to "remove" rings in order to get a
simpler ring system that would make a good starting point
for the drawing of the complete system.
May be it could be possible to enumerate these possibilities
without considering all atom number permutations.
This was my second question.

Jean-Marc Nuzillard
www.univ-reims.fr/LSD

Message de gilleain torrance <gilleain.torra...@gmail.com>:

> Hi,
>
> There is a way to get different graphs for the same molecule, but
> there will be quite a few of them for camphor. It has 11 atoms, and
> only one permutation that is automorphic (swapping the methyl groups
> attached to the bridgehead carbon), so there are 11! / 2 = 19,958,400
> permutations of the atoms. I'm not sure if there is a way to cut down
> this number.
>
> gilleain torrance
>
> On Mon, Mar 22, 2010 at 8:41 PM, JEAN MARC NUZILLARD
> <jm.nuzill...@univ-reims.fr> wrote:
>> Hi,
>>
>> I created two identical molecules by calling addAtoms and addBonds
>> in the same order with the same arguments and then I generated coordinates
>> using a StructureDiagramGenerator.
>> Looking with Jmol at the molecules in the corresponding SD file,
>> it appeared that the graphs were different.
>> Repeting the whole process, I sometimes get the same graphs,
>> but sometimes different ones.
>> The molecule is camphor. I am usign CDK-1.2.5.
>>
>> Is there a non-deterministic part in the SDG algorithm?
>> Is there a way to purposely get different graphs for the same molecule,
>> thus allowing the user to choose the best looking one?
>>
>> Jean-Marc Nuzillard
>> www.univ-reims.fr/LSD
>>
>>
>>
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