Serotonin Hydrogen Succinate
ADVERTISEMENT
- Molecular formula
- C14H18N2O5
- CAS Number
- 65004-53-5
- IUPAC Name
- 2-(5-hydroxy-1H-indol-3-yl)ethylammonium;4-hydroxy-4-oxo-butanoate
- Molecular Weight
- 309.34g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2400g/cm3
- Appearance
- can vary depending on the purity and form of the sample. It is often used in research settings relating to neurotransmitter function and studies.
- Synonyms
- Serotonin succinate
Identification
Interesting facts
Interesting Facts About 2-(5-Hydroxy-1H-Indol-3-yl)ethylammonium; 4-Hydroxy-4-oxo-butanoate
The compound 2-(5-hydroxy-1H-indol-3-yl)ethylammonium; 4-hydroxy-4-oxo-butanoate is a fascinating chemical that combines elements from biochemistry and medicinal chemistry. Here are some noteworthy aspects:
- Biological Relevance: This compound exhibits connections to indole metabolism, which is crucial as indoles occur naturally in many biological processes, including the synthesis of neurotransmitters.
- Structure and Stability: The bipartite structure of this compound demonstrates the interaction between an indole derivative and an α-keto acid, enriching its potential functionality in biochemical pathways.
- Potential Applications: Due to its organization, this compound might show promise in drug development, particularly in targeting metabolic pathways related to neurotransmission and hormonal regulation.
- Research Insights: The 5-hydroxy substitution on the indole ring enhances its ability to engage in various biochemical activities, possibly affecting enzyme kinetics.
- Historical Significance: Indole compounds have long been researched for their biological effects, emphasizing their role in nature as \emph{plant hormones} and \emph{neurotransmitter precursors}.
As scientists continue to explore this compound’s applications, the intersection of its structural properties and biological significance offers exciting opportunities for novel discoveries in the field of medicinal chemistry.