<div dir="ltr"><div dir="ltr">Hmm, when I was in the drug discovery canal, the "descriptors" that you could calculate from a SMILES string were legion. <div><br></div><div>Here's the list for RDKIT, <a href="https://www.rdkit.org/docs/GettingStartedInPython.html#list-of-available-descriptors">https://www.rdkit.org/docs/GettingStartedInPython.html#list-of-available-descriptors</a>. There are one bunch that depend entirely on the formula and molecular structure. Then there's a whole other bunch you can compute if you generate 3d structures for the molecules, possibly multiplied by the number of low energy structures the molecule can adopt.</div><div><br></div><div>What kind of plausibility were you looking for? Does the SMILES string specify a real molecule? That's hard. There are syntax errors in SMILES, failures to close rings, valency errors, charge errors. But there are lots of syntactically valid SMILES that won't match any known molecule, either because they're impossible or as yet to be determined. The pharmas all have their own lists of molecules of interest, but those are proprietary. Looks like there are various online databases, none that I'm familiar with. If the SMILES parses, you can try generating a 2d depiction and a 3d structure. Those will throw exceptions if things get too weird.</div><div><br></div><div>-- rec --</div><div><br></div><div>On Tue, Oct 12, 2021 at 3:22 PM Marcus Daniels <<a href="mailto:marcus@snoutfarm.com">marcus@snoutfarm.com</a>> wrote:<br></div></div><div class="gmail_quote"><blockquote class="gmail_quote" style="margin:0px 0px 0px 0.8ex;border-left:1px solid rgb(204,204,204);padding-left:1ex">
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<p class="MsoNormal">I was playing with RDKIT the other day, and it wasn’t obvious how to get a scalar quantity of plausibility of a molecule. It seems a SMILES string is right or wrong, and then maybe there are some warnings that can be trapped. However,
the benefits for search or fair sampling are different than the needs of correctness checks, which is deeper property. That isn’t quite a fit to the music example where aesthetic considerations are subjective.<u></u><u></u></p>
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<p class="MsoNormal"><b>From:</b> Friam <<a href="mailto:friam-bounces@redfish.com" target="_blank">friam-bounces@redfish.com</a>> <b>On Behalf Of
</b>Jon Zingale<br>
<b>Sent:</b> Tuesday, October 12, 2021 12:11 PM<br>
<b>To:</b> <a href="mailto:friam@redfish.com" target="_blank">friam@redfish.com</a><br>
<b>Subject:</b> Re: [FRIAM] Schwill Rock?<u></u><u></u></p>
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<p class="MsoNormal"><span style="font-size:12pt;font-family:Verdana,sans-serif;color:rgb(51,51,51)">"</span><span style="font-size:12pt;font-family:Arial,sans-serif;color:black">I mean from the perspective of aesthetics. Understanding why Pandora is messing
it up means sampling the deep wells."</span><span style="font-size:12pt;font-family:Verdana,sans-serif;color:rgb(51,51,51)"><u></u><u></u></span></p>
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<p class="MsoNormal"><span style="font-size:12pt;font-family:Arial,sans-serif;color:black">Yes, but not more than one has to. This is why I am advocating for methods like a weighted ensemble. The working analogy for me comes from drug discovery. It doesn't
make a lot of sense to probe the same old sites and the same old conformations.</span><span style="font-size:12pt;font-family:Verdana,sans-serif;color:rgb(51,51,51)"><u></u><u></u></span></p>
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