Talk:Tofisopam

levotofisopam
The other optical isomer unexpectedly lowered serum urate, which led to clinical trials for gout. --Nbauman (talk) 20:39, 15 December 2012 (UTC)

Analogues
US Patent 5288863 gives a large series of homologues. It seems that the molecule is optimized apart from substitution of the benzene ring and that an EWG at the 2 position gives the strongest analogues (x3.77 stronger than tofisopam). The chemistry appears to use lithium perchlorate etherate for ring-expansion (O swapped for hydrazine). Friskly perchlorates are NOT something to be taken lightly. — Preceding unsigned comment added by Dvwynn (talk • contribs) 13:41, 26 October 2014 (UTC)

External links modified
Hello fellow Wikipedians,

I have just added archive links to 1 one external link on Tofisopam. Please take a moment to review my edit. If necessary, add after the link to keep me from modifying it. Alternatively, you can add to keep me off the page altogether. I made the following changes:
 * Added archive https://web.archive.org/20050502010007/http://www.velapharm.com:80/news/press050104.html to http://www.velapharm.com/news/press050104.html

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Cheers.—cyberbot II  Talk to my owner :Online 22:54, 14 January 2016 (UTC)