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N-Methylanhalinine

From Wikipedia, the free encyclopedia
N-Methylanhalinine
Names
IUPAC name
6,7,8-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline
Other names
1,2,3,4-Tetrahydro-6,7,8-trimethoxy-2-methylisoquinoline;O-Methylanhalidine
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C13H19NO3/c1-14-6-5-9-7-11(15-2)13(17-4)12(16-3)10(9)8-14/h7H,5-6,8H2,1-4H3
    Key: WMHZXZCCGOMWEQ-UHFFFAOYSA-N
  • CN1CCC2=CC(=C(C(=C2C1)OC)OC)OC
Properties
C13H19NO3
Molar mass237.299 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

N-Methylanhalinine, also known asO-methylanhalidine, is atetrahydroisoquinolinealkaloid found in variousTurbinicarpuscactus species.[1][2][3] It has been found to act as apotentinverse agonist of theserotonin5-HT7 receptor.[4] The compound is several-fold more potent as a serotonin 5-HT7 receptor inverse agonist than itsparent compoundanhalinine.[4]

See also

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References

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  1. ^Štarha, Roman; Chybidziurová, Adéla; Lacný, Zdenek (1999)."Alkaloids of the genus Turbinicarpus (Cactaceae)".Biochemical Systematics and Ecology.27 (8):839–841.Bibcode:1999BioSE..27..839S.doi:10.1016/S0305-1978(99)00019-8. Retrieved21 May 2025.
  2. ^Keeper Trout & friends (2013).Trout's Notes on The Cactus Alkaloids Nomenclature, Physical properties, Pharmacology & Occurrences (Sacred Cacti Fourth Edition, Part C: Cactus Chemistry: Section 1)(PDF). Mydriatic Productions/Better Days Publishing.
  3. ^Reti, L. (1954). "Chapter 26 Simple Isoquinoline Alkaloids".The Alkaloids: Chemistry and Physiology. Vol. 4. Elsevier. p. 7–21.doi:10.1016/s1876-0813(08)60153-0.ISBN 978-0-12-469504-7. Retrieved21 May 2025.{{cite book}}:ISBN / Date incompatibility (help)
  4. ^abChan 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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