The Vespiary

The Hive => Serious Chemistry => Topic started by: dormouse on April 19, 2000, 10:14:00 AM

Title: Fentanyl analogue -hypo
Post by: dormouse on April 19, 2000, 10:14:00 AM
Author  Topic:   Fentanyl analogue 
hypo
Member   posted 12-25-1999 10:53 AM          
--------------------------------------------------------------------------------
I stumbled on this article: Iwasawa Y. et al: J. Med. Chem. 42/25 (Dec. 16), 1, (1999).
It describes opioid antagonists of fentanyl class. But compound 13 seems to be pretty good, unselective agonist binder (low nanomolar binding constants). The compound has alpha(o-chlorophenethyl) on 1-N (instead of beta phenethyl) and 2-benzimidazolone-1-yl instead of N-phenylpropionamide. Does anyone have an idea how this substitution pattern can affect the bioactivity?
Did anyone try to put an OH group in meta or ortho-position of the aniline phenyl?
Appreciate your input.



Title: ORL-1 receptor agonist
Post by: Rhodium on September 09, 2002, 06:18:00 AM
This seems to be a very special opioid agonist, because it does not bind to any of the ordinary opioid receptors, but instead the ORL-1 receptor. Read the article at

https://www.thevespiary.org/rhodium/Rhodium/pdf/orl1.agonist.pdf (https://www.thevespiary.org/rhodium/Rhodium/pdf/orl1.agonist.pdf)



Compound 13 is the agonist, the others are antagonists.

Title: Receptors
Post by: Cyrax on September 09, 2002, 07:44:00 AM
This is a nice review of the different kind of opioid receptors:

http://www.tocris.com/opioidreview.htm (http://www.tocris.com/opioidreview.htm)



There are also links to cannabinoid, dopamine, GABA, ... receptors - with a lot of refs.