Anhalamine

In this article we will talk about Anhalamine and its relevance in different contexts. Anhalamine has become a topic of interest and debate in today's society, since its impact ranges from personal aspects to global repercussions. Throughout history, Anhalamine has played a fundamental role in various spheres, influencing the way we relate, consume information, and make decisions. In this article we will explore the different aspects that make Anhalamine an important topic today, as well as its evolution over time and its influence on contemporary society.

Anhalamine
Names
Preferred IUPAC name
6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinolin-8-ol
Identifiers
3D model (JSmol)
ChemSpider
KEGG
UNII
  • InChI=1S/C11H15NO3/c1-14-9-5-7-3-4-12-6-8(7)10(13)11(9)15-2/h5,12-13H,3-4,6H2,1-2H3
    Key: DVQVXTPSJBCBJI-UHFFFAOYSA-N
  • InChI=1/C11H15NO3/c1-14-9-5-7-3-4-12-6-8(7)10(13)11(9)15-2/h5,12-13H,3-4,6H2,1-2H3
    Key: DVQVXTPSJBCBJI-UHFFFAOYAR
  • COC1=C(C(=C2CNCCC2=C1)O)OC
Properties
C11H15NO3
Molar mass 209.245 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).

Anhalamine is a naturally occurring alkaloid which can be isolated from Lophophora williamsii.[1] It is structurally related to mescaline.[2]

See also

References

  1. ^ Lundström, J; Agurell, S (August 1968). "Biosynthesis of mescaline and anhalamine in peyote. IIa". Tetrahedron Letters. 9 (42): 4437–40. doi:10.1016/s0040-4039(01)99153-1. PMID 5672059.
  2. ^ Ghansah, E.; Kopsombut, P.; Maleque, M.A.; Brossi, A. (February 1993). "Effects of mescaline and some of its analogs on cholinergic neuromuscular transmission". Neuropharmacology. 32 (2): 169–174. doi:10.1016/0028-3908(93)90097-M. PMID 8383816. S2CID 42388554.


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