Difference between revisions of "25I-NBOH"

From DMT-Nexus Wiki
Jump to: navigation, search
(Links)
Line 21: Line 21:
 
* isomerdesign.com: [http://isomerdesign.com/PiHKAL/explore.php?domain=pk&id=5379 25I-NBOH]
 
* isomerdesign.com: [http://isomerdesign.com/PiHKAL/explore.php?domain=pk&id=5379 25I-NBOH]
 
* wikipedia.org: [https://en.wikipedia.org/wiki/25I-NBOH 25I-NBOH]
 
* wikipedia.org: [https://en.wikipedia.org/wiki/25I-NBOH 25I-NBOH]
 +
* eve-rave.ch: [http://eve-rave.ch/Forum/viewtopic.php?f=53&t=32464 25i/c-nboh] (German)
 +
* drugs-forum.com: [http://www.drugs-forum.com/forum/showthread.php?t=95632 25I-NBOH Experiences]
  
 
== Reference ==
 
== Reference ==

Revision as of 13:40, 19 April 2014

Safety profile Note error.png
Category:
  • Psychedelic
Main effects:
  • Open and closed eye visuals, euphoria, change in perception of time
Side effects:
  • Nausea (possible), vasoconstriction(mostly when combined with other vasoconstricting substances like LSD), unusual body sensations (facial flushing, chills, goosebumps, body energy), slight increase in heart rate, difficulty focusing (possible)
Health risks:
  • paranoia (possible), fear (possible), panic (possible), dystonia (rare), seizure (rare), death (rare)
Important safety remarks:
  • 25I-NBOH is a very new substance, with little known about its pharmacological or behavioral risks. The LD50 (median lethal dose) is not known.
  • Elaborate studies on this substance have not been performed, so long term effects are UNKNOWN!
  • Warning: This chemical is active in the microgram (µg) range! Please use extreme caution if working with this substance, a milligram scale and liquid measurement are VITAL! Please start with doses of 500µg or less!


25I-NBOH (NBOH-2CI, Cimbi-27) is a derivative of the phenethylamine derived hallucinogen 2C-I. It acts as a potent agonist for the 5HT2A receptor, with a Ki of 0.061nM at the human 5HT2A receptor, similar to the better-known compound 25I-NBOMe, making it some twelve times the potency of 2C-I itself.

It was discovered in 2006 by a team at Purdue University.

Links

Reference