From Wikipedia, the free encyclopedia
3-Methoxymethamphetamine
Legal status
Legal status
Identifiers
  • 1-(3-methoxyphenyl)-N-methyl-propan-2-amine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard ( EPA)
Chemical and physical data
FormulaC11H17NO
Molar mass179.263 g·mol−1
3D model ( JSmol)
  • CNC(C)Cc(c1)cccc1OC
  • InChI=1S/C11H17NO/c1-9(12-2)7-10-5-4-6-11(8-10)13-3/h4-6,8-9,12H,7H2,1-3H3 checkY
  • Key:USQWRDRXXKZFDI-UHFFFAOYSA-N checkY
 ☒NcheckY  (what is this?)   (verify)

3-Methoxymethamphetamine (also known as meta-methoxymethamphetamine or MMMA), which is most closely related to 3-methoxyamphetamine and PMMA and shares similar monoamine releasing effects, although its effects have not been studied so extensively as other related drugs. [1] It is an agonist of human TAAR1. [2]

See also

References

  1. ^ Dal Cason TA (June 2001). "A re-examination of the mono-methoxy positional ring isomers of amphetamine, methamphetamine and phenyl-2-propanone". Forensic Science International. 119 (2): 168–194. doi: 10.1016/S0379-0738(00)00425-4. PMID  11376983.
  2. ^ Lewin AH, Miller GM, Gilmour B (December 2011). "Trace amine-associated receptor 1 is a stereoselective binding site for compounds in the amphetamine class". Bioorganic & Medicinal Chemistry. 19 (23): 7044–7048. doi: 10.1016/j.bmc.2011.10.007. PMC  3236098. PMID  22037049.
From Wikipedia, the free encyclopedia
3-Methoxymethamphetamine
Legal status
Legal status
Identifiers
  • 1-(3-methoxyphenyl)-N-methyl-propan-2-amine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard ( EPA)
Chemical and physical data
FormulaC11H17NO
Molar mass179.263 g·mol−1
3D model ( JSmol)
  • CNC(C)Cc(c1)cccc1OC
  • InChI=1S/C11H17NO/c1-9(12-2)7-10-5-4-6-11(8-10)13-3/h4-6,8-9,12H,7H2,1-3H3 checkY
  • Key:USQWRDRXXKZFDI-UHFFFAOYSA-N checkY
 ☒NcheckY  (what is this?)   (verify)

3-Methoxymethamphetamine (also known as meta-methoxymethamphetamine or MMMA), which is most closely related to 3-methoxyamphetamine and PMMA and shares similar monoamine releasing effects, although its effects have not been studied so extensively as other related drugs. [1] It is an agonist of human TAAR1. [2]

See also

References

  1. ^ Dal Cason TA (June 2001). "A re-examination of the mono-methoxy positional ring isomers of amphetamine, methamphetamine and phenyl-2-propanone". Forensic Science International. 119 (2): 168–194. doi: 10.1016/S0379-0738(00)00425-4. PMID  11376983.
  2. ^ Lewin AH, Miller GM, Gilmour B (December 2011). "Trace amine-associated receptor 1 is a stereoselective binding site for compounds in the amphetamine class". Bioorganic & Medicinal Chemistry. 19 (23): 7044–7048. doi: 10.1016/j.bmc.2011.10.007. PMC  3236098. PMID  22037049.

Videos

Youtube | Vimeo | Bing

Websites

Google | Yahoo | Bing

Encyclopedia

Google | Yahoo | Bing

Facebook