Penicillin G
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- Molecular formula
- C16H18N2O6S
- CAS Number
- 69-57-8
- IUPAC Name
- 2-amino-5-[[2-(carboxymethylamino)-2-oxo-1-(sulfosulfanylmethyl)ethyl]amino]-5-oxo-pentanoic acid
- Molecular Weight
- 333.36g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.6680g/cm3
- Synonyms
- SCHEMBL9188225
Identification
Interesting facts
Interesting Facts about 2-amino-5-[[2-(carboxymethylamino)-2-oxo-1-(sulfosulfanylmethyl)ethyl]amino]-5-oxo-pentanoic Acid
This fascinating compound is a member of the amino acid derivatives, showcasing a unique structure that makes it noteworthy in the field of biochemistry. Here are some compelling aspects:
- Complex Structure: The compound features multiple functional groups, including carboxymethyl, amino, and sulfonyl moieties, contributing to its structural complexity and potential biological activity.
- Potential Biological Role: Its structure suggests it could play a role in metabolic pathways, possibly acting as a precursor or derivative in synthesis processes related to amino acids and proteins.
- Research Applications: Compounds like this one are often studied in relation to therapeutic applications, particularly in the fields of drug development and biochemical research. The presence of the sulfosulfanylmethyl group may indicate applications in pharmaceuticals or agricultural chemistry.
- Noteworthy Mechanism: Research surrounding similar compounds reveals they may exhibit enzyme-inhibitory properties, which could be of great interest in the design of inhibitors for specific metabolic pathways.
- Potential Environmental Significance: Given its structure, it might also show properties related to environmental sustainability, especially in bioremediation or as a biodegradable alternative in various applications.
As we delve deeper into the chemical properties and implications of 2-amino-5-[[2-(carboxymethylamino)-2-oxo-1-(sulfosulfanylmethyl)ethyl]amino]-5-oxo-pentanoic acid, it becomes clear that its intricate design underlines the remarkable complexity of biochemical interactions and the potential for innovative research avenues.