Talk:Simplified molecular input line entry specification
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To be honest, I'm a SMILES novice, though I've known of its existence for years.
An unambiguous depiction of the atomic structure of molecules is crucial to successfully depicting and communicating about chemistry. Images are often indispensible to such depiction. However, there are a number of issues surrounding the generation and inclusion of images in the Wikipedia (transcluded links hosted offsite aren't part of the central encyclopedia corpus, easy software support of image loading isn't available or if available brings concern of abuse, images seem to generate more copyright concern [whether justified or not] than words contributed, etc.)
It seems that SMILES strings can serve as a very compact adjunct for depicting some molecular structures.
I encourage my fellow Wikipedian science authors to consider the use of SMILES strings in their work.
--JoeAnderson
- Yes, it would certainly be a nice piece of information to add. Less for depiction perhaps, but it would certainly make information more searchable. Search by substructure would certainly be a nice thing to have.
Shyamal 12:56, 30 Jun 2004 (UTC)
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[edit] Leaving atoms out
I noticed that the SMILES representations for Citric Acid and Calcium citrate do not show the hydrogen atoms consistently. What is the deal? Say you draw a structure without H's, do you show the SMILES for the structure you drew, or for the molecule as it exists in reality? --Slashme 09:45, 27 October 2005 (UTC)
- I can't find the examples you mention, however, in general, there are multiple ways to represent almost any given structure using almost any desired notation system. For SMILES, it's okay to omit an explicit H when the atom is attached to the "organic subset" and the number of them is obvious (from valence rules). It's also okay to include them explicitly if you want, either in the square brackets or as explicit attached substituents. That's pretty close to the rule for most structural diagrams, too: you can omit hydrogen from carbon (but not the rest of the SMILES organic subset!) if you want, or you can include some or all of them if it makes the structure more clearly illustrate whatever you're trying to illustrate with it. DMacks 04:52, 26 January 2006 (UTC)
[edit] Page title
Any reason why SMILES redirects to Simplified molecular input line entry specification instead of the other way around? I assume SMILES is the most common name. National Aeronautics and Space Administration redirects to NASA, American Standard Code for Information Interchange redirects to ASCII, etc. Not a major problem, but it looks inconsistent. 82.92.119.11 19:17, 14 June 2006 (UTC)
[edit] SLN Link
The link to SLN leads to a page a boutdurch sign language. Should it not be changed for something of the sort of ‘SLN (Tripos)’? 11:57, 17 September 2006 (UTC)
- According to be bold! you are encouraged to edit things on your own. Anyway, I have created a SYBYL Line Notation article which is now cross-linked in both directions. Kind regards, JKW 20:29, 17 September 2006 (UTC)
[edit] External Links
To my mind, we should include ones directly related to SMILES itself: SMILES and SMARTS, and the tutorial seems in keeping with WP:EL. The Parsing SMILES technical page seems on-topic as well. The links to various converters and products that happen to understand SMILES seem inappropriate. It gets off the topic of SMILES as a syntax and system into just a collection of ext-links (specifically discouraged by WP:EL). The list is woefully incomplete both for products listed and whole classes of things (SMILES is at least as important as a database tool than just converting to/from 2D structures) and draws focus towards a few specific implementations that may not even be the most featured/general/useful ones (inescapable POV or undue weight issues). DMacks 00:15, 24 January 2007 (UTC)
- That's along the lines of what I was thinking, although I don't really know the topic. I just dropped by to clean up after a conflict of interest editor who seemed to be over-linking his own work to a number of articles. I noticed the other links seemed to be straying so added the cleanup tag. ✤ JonHarder talk 01:11, 24 January 2007 (UTC)
[edit] Inorganic molecules
I'm an inorganic chemist, and after reading the current form of the article I don't feel able to estimate if (or how) this works for transition metal complexes (not necessarily mononuclear... say big polyoxometalates). Inorganic mixed-valence systems would also pose an interesting problem. Probably the article should give an idea of to what extent this works for inorganic systems. -- 147.156.44.37 17:02, 15 February 2007 (UTC)
