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Anhalidine

From Wikipedia, the free encyclopedia
Anhalidine
Names
Preferred IUPAC name
6,7-Dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-8-ol
Identifiers
3D model (JSmol)
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
C12H17NO3
Molar mass223.272 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Anhalidine is a naturally occurringtetrahydroisoquinoline basedalkaloid which can be isolated fromLophophora williamsii;[1] it has also been detected othercactii[2] and several species ofAcacia.[3][4] It is part of a family of compounds that are structurally related tomescaline. Anhalidine has been found to act as apotentinverse agonist of theserotonin5-HT7 receptor.[5]

See also

[edit]

References

[edit]
  1. ^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.
  2. ^Roush, Robin A.; Cooks, R. Graham.; Sweetana, Stephanie A.; McLaughlin, Jerry L. (1985). "Search for new alkaloids inPachycereus weberi by tandem mass spectrometry".Analytical Chemistry.57 (1):109–114.doi:10.1021/ac00279a030.ISSN 0003-2700.PMID 3985330.
  3. ^Clement, Beverly A.; Goff, Christina M.; Forbes, T. David A. (1997). "Toxic amines and alkaloids fromAcacia berlandieri".Phytochemistry.46 (2):249–254.Bibcode:1997PChem..46..249C.doi:10.1016/S0031-9422(97)00240-9.ISSN 0031-9422.
  4. ^Clement, Beverly A; Goff, Christina M; Forbes, T.David A (1998). "Toxic amines and alkaloids fromAcacia rigidula".Phytochemistry.49 (5):1377–1380.Bibcode:1998PChem..49.1377C.doi:10.1016/S0031-9422(97)01022-4.ISSN 0031-9422.
  5. ^Chan CB, Pottie E, Simon IA, Rossebø AG, Herth MM, Harpsøe K, Kristensen JL, Stove CP, Poulie CB (February 2025). "Synthesis, Pharmacological Characterization, and Binding Mode Analysis of 8-Hydroxy-Tetrahydroisoquinolines as 5-HT7 Receptor Inverse Agonists".ACS Chem Neurosci.16 (3):439–451.doi:10.1021/acschemneuro.4c00667.PMID 39836645.

External links

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5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
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