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Serotonin 5-HT2A receptor agonist · Serotonergic psychedelic · Hallucinogen

BMB-202

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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][5–9] WP

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][2] WP

Chemistry

Awaiting sourceFormula, structure and identifiers from PubChem.

Harm reduction information

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Sources

  1. Journal / agency BMB 202. 24 April 2023
  2. Other Delving into the Latest Updates on BMB-202 with Synapse. 29 October 2024
  3. 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
  4. Other Bright Minds Biosciences Provides Clinical Program Updates and Outlines Anticipated Milestones for 2023. 27 February 2023
  5. Other Bright Minds Biosciences Receives a Favorable Written Opinion from the International Searching Authority for BMB-202. 19 April 2023
  6. Other Bright Minds Biosciences. Bright Minds Novel Drugs for Targeted Treatment of CNS & Neuropsychiatric Disorders September 2024 (BMB Investor Deck). September 2024
  7. Other Vasilkevich A, Lovera A, Duan J, McDonald I, Collins SD, Pedersen JT. Overview of Bright Minds Biosciences: Pioneering Serotonin Pharmacology. 7 December 2025
  8. 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
  9. 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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