BMB-202
Overview
BMB-202 is a selective serotonin 5-HT2A receptor agonist and psychedelic drug of the N-benzylphenethylamine family which is under development for the treatment of depressive disorders and post-traumatic stress disorder (PTSD). It is taken orally.[1–7] WP
Drug class
Serotonin 5-HT2A receptor agonist Serotonergic psychedelic Hallucinogen WP
From the Wikipedia article's infobox.
Pharmacology
Pharmacodynamics
BMB-202 acts as a highly selective full agonist of the serotonin 5-HT2A receptor. In terms of EC₅₀ (half-maximal effective concentration) values, it shows 36- to 40-fold selectivity for activation of the serotonin 5-HT2A receptor over the serotonin 5-HT2C receptor and 500-fold selectivity for activation of the serotonin 5-HT2A receptor over the serotonin 5-HT2B receptor. It has been claimed by its developer that BMB-202 is the most selective serotonin 5-HT2A receptor agonist yet to be discovered or to be in development, at least as of late 2024.[1–7] WP
BMB-202 induces the head-twitch response (HTR), a behavioral proxy of psychedelic effects, in animals. Hence, it is putatively hallucinogenic in humans. As with other psychedelics like psilocybin, the HTR induced by BMB-202 shows a biphasic or inverted U-shaped dose–response curve.[3] WP
The drug shows a pharmacokinetic profile of high peak levels, rapid metabolic clearance, and a short elimination half-life in animals. It is predicted that BMB-202 will have a short half-life of less than 2 hours and short duration of 1 to 2 hours in humans. In relation to this, the drug is described as a "fast-on-fast-off" compound. The expected short duration of BMB-202 is analogous to the short duration of dimethyltryptamine (DMT). Short-acting psychedelics like DMT and BMB-202 may be more suitable for use in clinical therapeutic settings. BMB-202 is also described as having rapid absorption and brain distribution, high bioavailability, and significant first-pass metabolism resulting in it being fast-acting and having a short duration.[3]
Research
Research
BMB-202 is under development by Bright Minds Biosciences. As of September 2025, it is in the preclinical research stage of development for treatment of depressive disorders and PTSD.[1]
Chemistry
Harm reduction information
No harm reduction data is on file for this compound yet. That means no dose, timing or combination data from PsychonautWiki or TripSit. Please don't guess a dose from similar compounds. If you have taken it and feel unwell, contact emergency services or a poison control center.
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Sources
- Journal / agency BMB 202. 24 April 2023
- Other Delving into the Latest Updates on BMB-202 with Synapse. 29 October 2024
- Other Vasilkevich A, Halberstadt AL, Duan J, Merritt CR, Cunningham KA, McCorvy J, Kozikowski A, Pedersen J. Novel 5-HT2A selective agonists with well-characterized PK profile and short duration of action. October 2024
- Other Bright Minds Biosciences Provides Clinical Program Updates and Outlines Anticipated Milestones for 2023. 27 February 2023
- Other Bright Minds Biosciences Receives a Favorable Written Opinion from the International Searching Authority for BMB-202. 19 April 2023
- Other Bright Minds Biosciences. Bright Minds Novel Drugs for Targeted Treatment of CNS & Neuropsychiatric Disorders September 2024 (BMB Investor Deck). September 2024
- Other Vasilkevich A, Lovera A, Duan J, McDonald I, Collins SD, Pedersen JT. Overview of Bright Minds Biosciences: Pioneering Serotonin Pharmacology. 7 December 2025
- Journal / agency Cameron LP, Olson DE. Dark Classics in Chemical Neuroscience: N, N-Dimethyltryptamine (DMT). ACS Chem Neurosci. October 2018. doi:10.1021/acschemneuro.8b00101 · PMID 30036036
- Journal / agency Chaves C, Dos Santos RG, Dursun SM, Tusconi M, Carta MG, Brietzke E, Hallak JE. Why N, N-Dimethyltryptamine (DMT) Matters: Unique Features and Therapeutic Potential Beyond Classical Psychedelics. Frontiers in Psychiatry. 2024. doi:10.3389/fpsyt.2024.1485337 · PMID 39568756 · PMC11576444
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