Interesting facts
Interesting Facts about 2-acetamido-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic acid
This compound, also known for its role in medicinal chemistry, is of particular interest for its potential applications in pharmaceuticals. Here are some compelling facts that highlight its significance:
- Medicinal Potential: This compound is related to anticancer agents, and its structure suggests promising activity against various types of tumors.
- Mechanism of Action: The presence of the bis(2-chloroethyl)amino group is crucial, as it forms a reactive alkylating agent, which can interact with DNA, potentially stopping cancer cell proliferation.
- Structure Activity Relationship (SAR): Understanding the precise influence of the acetamido and phenyl groups on the biological activity is a key area of research, helping scientists design more effective derivatives.
- Analytical Techniques: Researchers utilize advanced analytical methods, such as NMR spectroscopy and mass spectrometry, to study the compound's dynamics and confirm its structure.
- Research Significance: Ongoing studies explore this compound's role in targeted therapy, aiming to reduce side effects common in traditional chemotherapy.
With its intricate structure and promising pharmacological properties, 2-acetamido-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic acid exemplifies the exciting intersections of chemistry and medicine. As noted by many scientists, "The journey to understanding this compound may uncover new pathways to combat cancer." The ongoing work surrounding it emphasizes the critical importance of chemical innovation in advancing healthcare.
Synonyms
N-Acetylmelphalan
N-Acetylsarcolysine
Acetylsarcolysine
1160-90-3
5786-56-1
2-acetamido-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic acid
DL-Phenylalanine, N-acetyl-4-[bis(2-chloroethyl)amino]-
N-Acmel
DL-Phenylalanine, N-acetyl-4-(bis(2-chloroethyl)amino)-
Phenylalanine, N-acetyl-4-(bis(2-chloroethyl)amino)-
NSC 212512
ALANINE, N-ACETYL-3-(p-(BIS(2-CHLOROETHYL)AMINO)PHENYL)-
MLS000123340
SCHEMBL6661149
CHEMBL1406831
L-Phenylalanine, N-acetyl-4-[bis(2-chloroethyl)amino]-
DTXSID90921896
NZEYWBNQKCRBFO-UHFFFAOYSA-N
HMS2470G07
NSC154852
NSC212512
2-Acetylamino-3-{4-[bis-(2-chloro-ethyl)-amino]-phenyl}-propionic acid
AKOS000588937
AKOS024304113
NSC-154852
NSC-212512
NCGC00245095-01
SMR000124012
SR-01000319133
SR-01000319133-1
N-acetyl-4-[bis(2-chloroethyl)amino]-dl-phenylalanine
2-acetylamino-3-{4-[bis(2-chloroethyl)amino]phenyl}propionic acid
4-[Bis(2-chloroethyl)amino]-N-(1-hydroxyethylidene)phenylalanine
Alanine, N-acetyl-3-(p-(bis(2-chloroethyl)amino)phenyl)-, DL-
Solubility of 2-acetamido-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic acid
The solubility of 2-acetamido-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic acid presents an intriguing profile due to its complex molecular structure. Understanding its solubility characteristics can provide insight into its applications and behavior in various environments. Here are some important points to consider:
As a rule of thumb, it’s often stated that “like dissolves like,” meaning that polar compounds will generally have better solubility in polar solvents, while non-polar compounds prefer non-polar solvents. For 2-acetamido-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic acid, its unique blend of functionalities suggests a moderate solubility behavior that merits further experimental investigation.