Tryptamine-5-carboxamide

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Identification

Molecular formula
C11H13N3O
CAS Number
14639-25-9
IUPAC Name
3-(2-aminoethyl)-1H-indole-5-carboxamide
Molecular Weight
203.24g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2670g/cm3
Synonyms
5-Carboxamidotryptamine
Interesting facts

Interesting Facts about 3-(2-aminoethyl)-1H-indole-5-carboxamide

3-(2-aminoethyl)-1H-indole-5-carboxamide, also known as a derivative of indole, is a fascinating compound notable for its biological and medicinal significance. Here are some key points to consider:

  • Biological Relevance: This compound is recognized for its role in various biochemical pathways, particularly in relation to neurotransmitter modulation.
  • Medicinal Applications: Research indicates that derivatives of indole compounds may exhibit potential therapeutic effects, including anti-cancer properties and neuroprotective activities.
  • Structural Features: The indole ring system is a critical element, contributing to the compound’s unique properties. Indole’s ability to engage in various chemical interactions makes it a valuable scaffold in drug design.
  • Multifunctionality: Compounds containing aminoethyl groups often display increased solubility and can enhance bioavailability, making this compound a subject of interest in pharmacological studies.
  • Research Potential: Ongoing studies focus on its derivatives to explore novel therapeutic applications, particularly in treating neurodegenerative diseases.

As a student of chemistry, you might find it intriguing to explore the synthesis of this compound and its analogs. It presents a wonderful opportunity to understand indole chemistry and its implications in medicinal chemistry. As a mental note, remember: “The beauty of chemistry lies in its ability to connect molecular structures with biological functions.”

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