MET
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The JMC paper from 1985 (Vol. 28,p. 892) about various Methylisopropyltryptamines gives potency ranking in rats 5-MeO-MET>5-MeO-DMT>/=5-MeO-DET=4-HO-DMT>DET = 4-MeO-DMT=5-AcO-DMT>6-MeO-DMT>7-MeO-DMT.and in humans the rank order of potency in a series of N,N-Dialkyl-4-HO's was:
methyl-isopropyl>methyl-ethyl>methyl-methyl>methyl-propyl>ethyl-ethyl>isopropyl-isopropyl>
propyl-propyl>methyl-t-butyl..
The Methylethyl seems the best hybrid between oral activity and closeness
to dimethyl,activity in TIHKAL given with 80-100mg.
So 105mg was taken orally as the fumarat salt,equaling about 81mg base.
First effects were noted in 20min.,an initial tachycardie was attributed to "first time anxiety" as blood pressure and pulse remained unchanged through the whole experience.A rapid development from 25min to a +2 at 35' with some nausea lead to a peak at 50min.It was very optic in a DMT manner with CEV (green,red,blue) and lots of object shifting,color enhancement.And it had a very erotic feeling to it,altough I felt somewhat dizzy.Effects started to drop at 1h40min,not much left at 3h and completely out at 3.5h,"ready for the outside world" to cite TIHKAL.The only annoying side effect was a strong diuretic component at the comedown.
While not actually reaching a plus 3, I was surprised by this rather strong activity as DPT on the other hand is almost inactive p.o. in me,needing at least 200-250mg to get above a +1.MAO seems to have much more troubles with MET.
Maybe with higher doses one might be able to enter DMT world peroral?
Surely an interesting substitution pattern on the Indolethylenamin.