DMBMPP
DMBMPP, also known as juncosamine or as 2--6-piperidine, is a highly selective serotonin 5-HT2A receptor agonist and 2-benzylpiperidine analogue of the serotonergic psychedelic 25B-NBOMe which is used in scientific research.
Pharmacology
Pharmacodynamics
The -isomer is the most selective agonist for the human serotonin 5-HT2A receptor yet discovered, with a affinity of 2.5nM at the human serotonin 5-HT2A receptor and with 124-fold selectivity for the serotonin 5-HT2A receptor over the structurally similar serotonin 5-HT2C receptor. Together with 25CN-NBOH, -DMBMPP is the only known 5-HT2A agonist to exhibit this level of selectivity. In contrast to the case of the serotonin 5-HT2A receptor, no functional data has been reported for DMBMPP at the serotonin 5-HT2C receptor as of 2023.| Ligand | Ki ± SEM | Ki ± SEM | Ki ± SEM |
| ketanserin | mesulergine | fold selectivity | |
| h5-HT2A | h5-HT2C | h5-HT2C/h5-HT2A | |
| 2C-B | 6.0 ± 0.3 | 23.8 ± 2.6 | 9.5 |
| 25B-NBOMe | 0.19 ± 0.01 | 4.0 ± 0.4 | 21 |
| -DMBMPP | 5.3 ± 0.3 | 520 ± 22 | 98 |
| --DMBMPP | 2.5 ± 0.1 | 310 ± 42 | 124 |
| --DMBMPP | 2,100 ± 171 | 28,600 ± 4700 | 27 |
-DMBMPP was assessed and found to fully substitute for the psychedelic drug LSD in rodent drug discrimination tests. As such, DMBMPP may be expected to have hallucinogenic effects in humans.
Despite its uniquely high selectivity for the serotonin 5-HT2A receptor, it has been said that DMBMPP is not widely used as a pharmacological tool in scientific research, presumably due to its chemical synthesis being relatively inaccessible. Consequently, 25CN-NBOH, another highly selective serotonin 5-HT2A receptor agonist, has been proposed as an alternative to DMBMPP for use in scientific research. DMBMPP and 25CN-NBOH are the two most selective serotonin 5-HT2A receptor agonists known as of 2020.