From Wikipedia, the free encyclopedia
Anhalidine
Names
Preferred IUPAC name
6,7-Dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-8-ol
Identifiers
ChemSpider
UNII
InChI=1S/C12H17NO3/c1-13-5-4-8-6-10(15-2)12(16-3)11(14)9(8)7-13/h6,14H,4-5,7H2,1-3H3
Key: DTXOXOHMRGAFDX-UHFFFAOYSA-N
InChI=1/C12H17NO3/c1-13-5-4-8-6-10(15-2)12(16-3)11(14)9(8)7-13/h6,14H,4-5,7H2,1-3H3
Key: DTXOXOHMRGAFDX-UHFFFAOYAS
OC1=C(C(OC)=CC2=C1CN(C)CC2)OC
Properties
C 12 H 17 N O 3
Molar mass
223.272 g·mol−1
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound
Anhalidine is a naturally occurring
tetrahydroisoquinoline based
alkaloid which can be isolated from
Lophophora williamsii ;
[1] it has also been detected other
cactii
[2] and several species of
Acacia .
[3]
[4] It is part of a family of compounds that are structurally related to
mescaline .
See also
References
^ Lundström, Jan; Agurell, Stig (1967). "Thin-layer chromatography of the peyote alkaloids". Journal of Chromatography A . 30 (1): 271–272.
doi :
10.1016/S0021-9673(00)84157-6 .
ISSN
0021-9673 .
PMID
4293618 .
^ Roush, Robin A.; Cooks, R. Graham.; Sweetana, Stephanie A.; McLaughlin, Jerry L. (1985). "Search for new alkaloids in Pachycereus weberi by tandem mass spectrometry". Analytical Chemistry . 57 (1): 109–114.
doi :
10.1021/ac00279a030 .
ISSN
0003-2700 .
PMID
3985330 .
^ Clement, Beverly A.; Goff, Christina M.; Forbes, T. David A. (1997). "Toxic amines and alkaloids from Acacia berlandieri ". Phytochemistry . 46 (2): 249–254.
Bibcode :
1997PChem..46..249C .
doi :
10.1016/S0031-9422(97)00240-9 .
ISSN
0031-9422 .
^ Clement, Beverly A; Goff, Christina M; Forbes, T.David A (1998). "Toxic amines and alkaloids from Acacia rigidula ". Phytochemistry . 49 (5): 1377–1380.
Bibcode :
1998PChem..49.1377C .
doi :
10.1016/S0031-9422(97)01022-4 .
ISSN
0031-9422 .