6-Methoxytryptamine (CAS 3610-36-4)
QUICK LINKS
6-Methoxytryptamine is a chemical compound that functions as a serotonin receptor agonist in experimental applications. It interacts with serotonin receptors in the brain and other tissues, modulating their activity and influencing various physiological processes. At the molecular level, 6-Methoxytryptamine binds to specific serotonin receptor subtypes, triggering intracellular signaling cascades and altering cellular responses. 6-Methoxytryptamine′s mode of action involves the activation of serotonin receptors, leading to downstream effects on neurotransmission, mood regulation, and other biological functions. In development, 6-Methoxytryptamine is utilized to investigate the role of serotonin receptors in various physiological and pathological conditions, providing insights into the molecular mechanisms underlying these processes. Its ability to selectively target serotonin receptors makes it useful for studying the signaling pathways involved in neurotransmission and behavior.
6-Methoxytryptamine (CAS 3610-36-4) References
- Screening for endogenous substrates reveals that CYP2D6 is a 5-methoxyindolethylamine O-demethylase. | Yu, AM., et al. 2003. Pharmacogenetics. 13: 307-19. PMID: 12777961
- Inhibitory influence of late afternoon melatonin injections and the counter-inhibitory action of melatonin-containing pellets on thyroid growth process in male Wistar rats: comparison with effects of other indole substances. | Wajs, E. and Lewiński, A. 1992. J Pineal Res. 13: 158-66. PMID: 1287191
- Tandem intramolecular photocycloaddition-retro-Mannich fragmentation as a route to spiro[pyrrolidine-3,3'-oxindoles]. Total synthesis of (+/-)-coerulescine, (+/-)-horsfiline, (+/-)-elacomine, and (+/-)-6-deoxyelacomine. | White, JD., et al. 2010. J Org Chem. 75: 3569-77. PMID: 20429523
- Total synthesis of (±)-trigonoliimine C via oxidative rearrangement of an unsymmetrical bis-tryptamine. | Qi, X., et al. 2011. J Am Chem Soc. 133: 10050-3. PMID: 21671591
- Enantioselective total synthesis of (+)-reserpine. | Rajapaksa, NS., et al. 2013. Org Lett. 15: 706-9. PMID: 23331099
- Enantioselective Synthesis of (+)-Peganumine A. | Piemontesi, C., et al. 2016. J Am Chem Soc. 138: 11148-51. PMID: 27558528
- Nine-step total synthesis of (-)-strychnofoline. | Yu, Q., et al. 2018. Chem Commun (Camb). 54: 1125-1128. PMID: 29334094
- Engineered Production of Strictosidine and Analogues in Yeast. | Misa, J., et al. 2022. ACS Synth Biol. 11: 1639-1649. PMID: 35294193
- Synthesis and Antibacterial Study of Novel Harmine Derivatives and Tetrahydro-β-Carboline Derivatives In Vitro. | Liang, Y., et al. 2022. Molecules. 27: PMID: 35566239
- Enantioselective Syntheses of Yohimbine Alkaloids: Proving Grounds for New Catalytic Transformations. | Miller, ER. and Scheidt, KA. 2022. Synthesis (Stuttg). 54: 1217-1230. PMID: 36187077
- Divergent Asymmetric Total Synthesis of (-)-Voacafricines A and B. | Andres, R., et al. 2023. Angew Chem Int Ed Engl. 62: e202301517. PMID: 36825653
- The Engagement of Cytochrome P450 Enzymes in Tryptophan Metabolism. | Haduch, A., et al. 2023. Metabolites. 13: PMID: 37233670
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
6-Methoxytryptamine, 100 mg | sc-254891 | 100 mg | $62.00 | |||
6-Methoxytryptamine, 250 mg | sc-254891A | 250 mg | $135.00 |