Interesting facts
Interesting Facts about 2-[(2-formamido-4-methylsulfanyl-butanoyl)amino]-3-phenyl-propanoic acid
This compound is a fascinating example of medicinal chemistry due to its complex structure and functional groups. Here are some intriguing points to consider:
- Biological Importance: This compound contains an amino acid derivative that plays a crucial role in the development of various therapeutic agents.
- Functional Diversity: The presence of both a phenyl group and a sulfanyl group significantly enhances its chemical versatility, making it useful in various synthetic pathways.
- Potential Applications: Researchers are exploring its potential in anti-inflammatory and antimicrobial processes, highlighting the importance of structure-activity relationships in drug design.
- Analytical Techniques: Due to its unique properties, this compound can be analyzed using sophisticated techniques such as NMR spectroscopy and mass spectrometry, providing insights into its molecular behavior.
- Synthesis Challenges: The synthetic route to this compound can be quite complex, involving multiple steps of functional group interconversion and selective reactions.
In the words of a renowned chemist, "Understanding the intricacies of compounds like this offers an unparalleled glimpse into the world of chemical innovation." Indeed, the study of such compounds not only enhances our chemical knowledge but also opens up new avenues for drug discovery and development.
Overall, this compound serves as a reminder of the intricate relationship between structure and function in the realm of chemistry.
Synonyms
N-formylmethionylphenylalanine
FOR-MET-PHE-OH
Spectrum_001318
Spectrum2_001193
Spectrum3_001054
Spectrum4_001194
Spectrum5_001071
BSPBio_002608
KBioGR_001887
KBioSS_001798
DivK1c_000498
SPBio_001265
SCHEMBL3382813
CHEMBL3039207
HMS501I20
KBio1_000498
KBio2_001798
KBio2_004366
KBio2_006934
KBio3_001828
CHEBI:111175
NINDS_000498
CCG-40320
IDI1_000498
NCGC00178577-01
DB-045762
BRD-A09975616-001-02-3
Q27190675
2-[[2-formamido-4-(methylthio)-1-oxobutyl]amino]-3-phenylpropanoic acid
Solubility of 2-[(2-formamido-4-methylsulfanyl-butanoyl)amino]-3-phenyl-propanoic acid
This compound exhibits unique solubility characteristics due to its complex structure, incorporating both hydrophobic and hydrophilic portions. Understanding the solubility of such compounds can be crucial for their applications in pharmaceuticals and biochemistry.
Factors Affecting Solubility:
As a rule of thumb, compounds that are more polar tend to be more soluble in polar solvents, while non-polar parts can hinder solubility in such environments. Thus, this compound may be better soluble in mixed solvent systems or in conditions where its amino and carboxyl groups can engage in hydrogen bonding.
In summary, the solubility of 2-[(2-formamido-4-methylsulfanyl-butanoyl)amino]-3-phenyl-propanoic acid is influenced by its structural features and environmental conditions. As with many compounds, understanding these nuances can be pivotal in maximizing their potential use in various applications.