Tryptamines and derivatives
Tryptamines and their derivatives are a class of alkaloid compounds that play significant roles in various biological processes, particularly in the central nervous system (CNS). These compounds are characterized by a core structure consisting of an indole ring fused to a pyrrole ring. The most well-known tryptamine is L-tryptophan, one of the essential amino acids.
Derivatives of tryptamines often include substitutions at various positions on the indole and pyrrole rings, such as methyl groups or hydroxyl groups, which can alter their pharmacological properties. Notable examples include melatonin (N-acetyl-5-methoxytryptamine) and psilocybin (psilocin's prodrug form), both of which are known for their psychoactive effects.
In the pharmaceutical industry, tryptamines and their derivatives have been used to develop a wide range of drugs targeting various neurological disorders. For instance, certain antidepressants like fluoxetine contain structural elements reminiscent of tryptamine derivatives. Additionally, these compounds hold promise in treating conditions such as depression, anxiety, and even some forms of chronic pain.
Due to their complex structures and diverse biological activities, research into tryptamines continues to be a dynamic field in both academic and industrial settings.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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1H-Indole-3-ethanamine,2-methyl-5-nitro- | 28027-52-3 | C11H13N3O2 |
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5-Methoxy-N,N-diisopropyltryptamine Hydrochloride | 2426-63-3 | C17H27ClN2O |
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2-(5-Benzyloxy-1H-indol-3-yl)-ethylamine | 20776-45-8 | C17H18N2O |
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7-Methoxytryptamine | 2436-04-6 | C11H14N2O |
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1H-Indole-2-acetic acid, 3-[2-(3-ethyl-1-piperidinyl)ethyl]-α-(hydroxymethyl)-, methyl ester | 28423-88-3 | C21H30N2O3 |
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4-Piperidinamine,1-[2-(1-methyl-1H-indol-3-yl)ethyl]- | 26844-39-3 | C16H23N3 |
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1H-Indole-3-ethanamine,N,N,5,6,7-pentamethyl- | 25390-70-9 | C15H22N2 |
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N,N-5-Trimethyl-1H-indole-3-ethanamine | 22120-39-4 | C13H18N2 |
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4-Hydroxy-N,N-diethyltryptamine | 22204-89-3 | C14H20N2O |
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5-Cyanotryptamine | 46276-24-8 | C11H11N3 |
Related Literature
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Guang Xu,Wei Zhang,Ying Zhang,Xiaoxia Zhao,Ping Wen,Di Ma RSC Adv., 2018,8, 19353-19361
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J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
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Byungho Lim,Jaewon Jin,Jin Yoo,Seung Yong Han,Kyeongyeol Kim,Sungah Kang,Nojin Park,Sang Moon Lee,Hae Jin Kim,Seung Uk Son Chem. Commun., 2014,50, 7723-7726
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Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
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