Serotonin Hydroxycinnamate

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Identification

Molecular formula
C14H16N2O4
CAS Number
71610-00-9
IUPAC Name
2-(5-hydroxy-1H-indol-3-yl)ethylammonium;4-hydroxy-4-oxo-but-2-enoate
Molecular Weight
319.34g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.7000g/cm3
Interesting facts

Interesting Facts about 2-(5-hydroxy-1H-indol-3-yl)ethylammonium; 4-hydroxy-4-oxo-but-2-enoate

This compound is an intriguing example of a bi-functional molecule that interacts with both biological systems and synthetic processes. Here are some fascinating insights:

  • Biosynthetic Role: This compound is involved in various biosynthetic pathways, linking it to important metabolic processes in living organisms. The indole moiety is especially notable, as indole derivatives are common in many natural products and pharmaceuticals.
  • Interaction with Receptors: Due to its indole structure, this compound can potentially interact with serotonin receptors, making it a topic of interest in psychopharmacology. Researchers are investigating its implications in mood regulation and neurological functions.
  • Antioxidant Properties: The presence of hydroxy groups in its structure is often indicative of antioxidant activity. Compounds with phenolic structures can scavenge free radicals, which are damaging to biological tissues.
  • Potential Therapeutic Uses: Ongoing studies might reveal its utility in developing therapeutic agents for various conditions, including cancer and neurodegenerative diseases. The compound's unique structural features contribute to its potential efficacy.
  • Versatile Synthesis: The synthetic pathways to access this compound can include various methods of organic synthesis, highlighting its versatility and relevance in organic chemistry education.

As scientists continue to explore the complexity of such compounds, the potential applications in areas ranging from medicine to materials science remain vast. The study of 2-(5-hydroxy-1H-indol-3-yl)ethylammonium; 4-hydroxy-4-oxo-but-2-enoate exemplifies the intersection of chemistry, biology, and pharmacology.

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