Riemann Zeta
Bluelighter
DOI is likely safer and less toxic in terms of peripheral vasoconstrictive side effects--while it is a high-efficacy partial agonist at the 5-HT2A/B/C receptors (~70% of the response caused by 5-HT), DOB is an absolute full agonist (>100% of 5-HT response). For reference, ergoloids like LSD are around 40% in their agonist efficacy, as are tryptamines like psilocin/miprocin. Remember that agonist efficacy is different than agonist affinity, which is only a measurement of how tightly a given chemical sticks to a receptor, not how much it activates the receptor in comparison with the endogenous ligand. Obviously, DOI, DOB and LSD are all very high affinity 5-HT2A/C receptor agonists. Dose-wise, DOB is ever slightly more potent than DOI.
In terms of duration, however, DOI and DOB should be virtually identical. Given the choice, I'd take DOI every single time. In theory, DOC is supposed to be a little friendlier than DOI, which is friendlier than DOB. However, given a broader choice, I'd take neither and opt for the ergoloid. The 2,5-dimethoxy-4-halo-phenethylamine psychedelics cause way too much (that is, too long-lasting) tolerance for my enjoyment these days. Tolerance to the effects of something like LSD can be dissipated in around 7 days, 14 being optimal. Tolerance to DOI takes around a month to fully reset. Curiously, even though compounds like DMT and 5-MeO-DMT are also full agonists at the 5-HT2A/C receptors, tolerance to their effects resets after as little as 24 hours. Phenethylamines must cause a more profound downregulation of 5-HT2A receptors than tryptamines or ergoloids.
Some of those DOX compounds are really esoteric--I'd be interested in trying them maybe once, just for novelty's sake. I mean how often would someone encounter something like DOET or DOEF.
In terms of duration, however, DOI and DOB should be virtually identical. Given the choice, I'd take DOI every single time. In theory, DOC is supposed to be a little friendlier than DOI, which is friendlier than DOB. However, given a broader choice, I'd take neither and opt for the ergoloid. The 2,5-dimethoxy-4-halo-phenethylamine psychedelics cause way too much (that is, too long-lasting) tolerance for my enjoyment these days. Tolerance to the effects of something like LSD can be dissipated in around 7 days, 14 being optimal. Tolerance to DOI takes around a month to fully reset. Curiously, even though compounds like DMT and 5-MeO-DMT are also full agonists at the 5-HT2A/C receptors, tolerance to their effects resets after as little as 24 hours. Phenethylamines must cause a more profound downregulation of 5-HT2A receptors than tryptamines or ergoloids.
Some of those DOX compounds are really esoteric--I'd be interested in trying them maybe once, just for novelty's sake. I mean how often would someone encounter something like DOET or DOEF.
