I'm not in to pharmacology, but wtf haven't i seen any references of 4-tertButyl-2,5-DMPEA/DMA, 4-Isopropyl-2,5-DMPEA/DMA and the 4-Dimethylamine
homologue?
Haven't i looked to much, or is the groups not unpolar enough? Since alkyl-chains works, why not these?
Just wondering...
[Edited on 5-11-2006 by Dextrose]Sandmeyer - 4-11-2006 at 19:18
You have allready started a thread where this can be discussed, no need for a new one. Someone with more knowledge on SAR than me can provide a better
answer -- I think that tert-butyl is more likely to be an antagonist, the isopropyl might be interesting, dimethylamino would be inactive.Nicodem - 4-11-2006 at 23:52
Quote:
Originally posted by Dextrose
I'm not in to pharmacology, but wtf haven't i seen any references of 4-tertButyl-2,5-DMPEA/DMA, 4-Isopropyl-2,5-DMPEA/DMA and the 4-Dimethylamine
homologue?
Both branching and chirality of the 4-substituent in 2,5-DMA was evaluated by Nichols. See: J. Med. Chem., 1984, 27, 788-792. J. Med. Chem., 1995, 38, 3593-3601.
PS: I agree that there was no need whatsoever to start a new thread when you already started a thread on a very similar issue. This forum is not
intended to be a trash can!Drunkguy - 5-11-2006 at 06:28
It's also very convincing that the 4-allyloxy is stable as it is susally prone to a Claisen rearrangement.
[Edited on 5-11-2006 by Drunkguy]Dextrose - 8-11-2006 at 09:26
Sandmeyer, Nicodem > I'm sorry to piss you old hive-farts off (J/K).
I hate off-topicness, so i figured since this question is strictly pharmacology-related, i wouldn't dare going OT in my other topic, which is strictly
chemistry-related.
Thanks for the ref's Nicodem, will check them out.
