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5-Bromo-DMT: Wikis

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5-Bromo-DMT
5-Bromo-DMT.svg
IUPAC name
Identifiers
CAS number 17274-65-6
PubChem 360252
SMILES
Properties
Molecular formula C12H15N2Br
Melting point

98-99 °C

Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

5-Bromo-DMT (5-bromo-N,N-dimethyltryptamine) is a brominated indole alkaloid found in certain marine invertebrates. It is the 5-bromo analogue of DMT, a hallucinogen found in many plants and animals.[1] Other naturally occurring 5-substituted analogues of DMT include bufotenin and 5-MeO-DMT, both of which, like DMT, are psychoactive and found in plants and animals. Animal studies on 5-bromo-DMT showed it to produce effects suggestive of sedative and antidepressant activity.[2]

References

  1. ^ Djura, Peter et al. (1980). "Some Metabolites of the Marine Sponges Smenospongia aurea and Smenospongia (= Polyfibrospongia) echina". Journal of Organic Chemistry 45 (8): 1435–1441. doi:10.1021/jo01296a019.  
  2. ^ Kochanowska AJ, Rao KV, Childress S, El-Alfy A, Matsumoto RR, Kelly M, Stewart GS, Sufka KJ, Hamann MT (February 2008). "Secondary metabolites from three Florida sponges with antidepressant activity". Journal of Natural Products 71 (2): 186–9. doi:10.1021/np070371u. PMID 18217716.  
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5-Bromo-DMT
Identifiers
CAS number 17274-65-6
PubChem 360252
SMILES
Properties
Molecular formula C12H15N2Br
Melting point

98-99 °C

Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

5-Bromo-DMT (5-bromo-N,N-dimethyltryptamine) is a brominated indole alkaloid found in certain marine invertebrates. It is the 5-bromo analogue of DMT, a hallucinogen found in many plants and animals.[1] Other naturally occurring 5-substituted analogues of DMT include bufotenin and 5-MeO-DMT, both of which, like DMT, are psychoactive and found in plants and animals. Animal studies on 5-bromo-DMT showed it to produce effects suggestive of sedative and antidepressant activity.[2]

References

  1. ^ Djura, Peter et al. (1980). [Expression error: Unexpected < operator "Some Metabolites of the Marine Sponges Smenospongia aurea and Smenospongia (= Polyfibrospongia) echina"]. Journal of Organic Chemistry 45 (8): 1435–1441. doi:10.1021/jo01296a019. 
  2. ^ Kochanowska AJ, Rao KV, Childress S, El-Alfy A, Matsumoto RR, Kelly M, Stewart GS, Sufka KJ, Hamann MT (February 2008). [Expression error: Unexpected < operator "Secondary metabolites from three Florida sponges with antidepressant activity"]. Journal of Natural Products 71 (2): 186–9. doi:10.1021/np070371u. PMID 18217716. 

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