QUARE
Bluelighter
(RS)-2-(2-Chlorophenyl)-2-(methylamino)cyclohexane
-
N&PD Moderators: Skorpio
I Like to Draw Pictures of Random Molecules
- Thread starter nuke
- Start date
- Status
(RS)-2-(2-Chlorophenyl)-2-(methylamino)cyclohexane 
babylonboy
Bluelighter
- Joined
- Oct 30, 2012
- Messages
- 1,410
You'll know all about it as soon as AiHKAL is published.
QUARE
Bluelighter
is that a work in progress ?
ebola?
Bluelight Crew
Everyone wishes it were. . .
ebola
Incunabula
Bluelighter
- Joined
- Dec 10, 2010
- Messages
- 1,861
Shulgin didn't consider arylcyclohexylamines to be true psychedelic entheogens, and didn't care to do any reseach on them.
I think the ketamine analog I proposed without the keto must have been made? it's so obvious. And it must have increased duration than ketamine (?) Since the ketone is making it easier for the body to excrete it.
Funny thing is, as an analog you couldn't call it something with ketamine (like 2-meo-ketamine,n-ethyl-ketamine etc) because the "keta" in ketamine comes from ketone, and it would be pretty stupid to just call it "amine" 8)
Quare, you have some lazy software that writes the right IUPAC?
pharmakos
Bluelighter
desketamine?
babylonboy
Bluelighter
- Joined
- Oct 30, 2012
- Messages
- 1,410
Any software for drawing formulas will do this, I use Symyx Draw.
QUARE
Bluelighter
Nah, I simply replace the cyclohexanone for a cyclohexane on the ketamine IUPAC name and the molecule is draw from emolecules.comLast edited:
Jesusgreen
Bluelight Crew
(Remember I know fuck all about SAR :D if you're wondering why the second one - I based it on the fact that Mephtetramine appears to be active, even if people are reporting poor results. Wanted to make something that looks like it really wouldn't be active but that might be.)
Edit:
I was bored so here's a few more:
I'm guessing the second from last was already made and probably mentioned in PiHKAL somewhere but I was a bit too lazy to check.Last edited:
pharmakos
Bluelighter
bloodshed344
Bluelighter
- Joined
- May 9, 2012
- Messages
- 1,575
This one, along with another DMT analog where the indole ring is replaced with the thiophene ring has been made. Both are reportedly active. Read this on BL in a thread from like 2007 or 2009 or something.
Anon0631
Bluelighter
If MDAI is active, what about the DOx analogues?
pharmakos
Bluelighter
^ my completely amateur guess is that those would be active but substantially less potent
Anon0631
Bluelighter
I wonder how the experience would be.bloodshed344
Bluelighter
- Joined
- May 9, 2012
- Messages
- 1,575
If MDAI is active, what about the DOx analogues?
2C-B-Ind is what this is called. It's on wikipedia.
pharmakos
Bluelighter
2C-B-Ind isn't quite the same thing. this is from the 2C-B-Ind Wikipedia article:
the aminoindane version that anon posted looks more promising to me. 2C-B-Ind tries to squeeze an extra carbon atom in there.
Anon0631
Bluelighter
Why hasn't someone invented a machine where you can upload a picture and receive a couple of hundred milligrams of sample to experiment with. It would be much more efficient than all this speculation
Edit: Should the molecule be called DMAI-B?Last edited:
sekio
Bluelight Crew
it's called a computer
The rigid aminoindane analogue of DOM was made by Nichols in 1972, as well as the slightly more potent tetralin analogue. It's something close to 1/5 to 1/10 the potency of DOM and has a different character... more of a stimulant, apparently.
see Journal of Medicinal Chemistry 1974, vol. 17, p. 161
pharmakos
Bluelighter
Toz
Bluelighter
Why hasn't someone invented a machine where you can upload a picture and receive a couple of hundred milligrams of sample to experiment with. It would be much more efficient than all this speculation
Edit: Should the molecule be called DMAI-B?
it's on the way (or well at least someone has the right idea) :D
http://theweek.com/article/index/246091/can-you-3d-print-drugs- Status