Nice work. http://timvdm.blogspot.com/2009/09/automorphism-group-bliss.html

Does this mean you've solved the problem?

- Noel

2009/9/28 Tim Vandermeersch <tim.vandermeer...@gmail.com>:
> Hi,
>
> Using openbabel trunk there are still a number of cases where highly
> symmetric molecules can not be canonicalized. See my blog posts for
> examples: http://timvdm.blogspot.com
>
> To correctly select a minimum or maximum canonical labeling, I was
> planning to implement the algorithm from the 1993 Razinger paper on
> stereoisomer generation. The final result is a signed permutation
> matrix where equal rows represent the same stereoisomer. However,
> constructing these matrices requires the automorphism group of a
> structure. While I have some code to do this, a reasonably fast method
> is required for structures like inositol where the initial graph
> invariant atom partitioning still leaves us with 6! * 6! combinations.
> (See also: http://depth-first.com/articles/2009/09/15/stereoisomer-generation
> , 
> http://depth-first.com/articles/2009/09/16/stereochemistry-puzzler-how-many-stereoisomers-for-these-69-structures
> )
>
> Rich Apodaca suggested using the VFLib algorithm to limit the search
> space. However, my first attempt wasn't very successful and I thought
> it would be a good idea to get some input before I spent (or waste)
> more time on this. If I have to get to the bottom of the VFLib
> algorithm I'd prefer to write the isomorphism matcher for MolCore at
> the same time, hopefully reusing parts of RDKit. Another option would
> be to use bliss (small library, could be embedded,
> http://www.tcs.hut.fi/Software/bliss/index.html, MIT license) to get a
> set of generators of the automorphism group.
>
> Ideas or feedback would be very welcome. If someone is more familiar
> with permutation groups and wants to help, that would also be great
> :-)
>
> Cheers,
> Tim
>

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