ungelesene_bettlek
Bluelighter
- Joined
- Feb 15, 2006
- Messages
- 913
if one would attach another amino group at the 4-ethyl group of 2C-E, one would get a quite symmetric molecule. I wonder if this would be active...
if one would attach another amino group at the 4-ethyl group of 2C-E, one would get a quite symmetric molecule. I wonder if this would be active...
Doubtful, since the 4-substituent should be non-polar for good activity.
What about 2c-c and 2c-b? Or the Methoxy analog? No-sir. I believe he may have an active compound.
in general use nonpolar=hydrophobic
chloro bromo ethyl methoxy all hydrophobic.
\I can't see the compound being active especially with the hydrogen bonding. Additionally diamines are often potent HERG ligands. Tread very carefully. however 'Make em taste em' is the only sure way to know.