Interesting facts
Interesting Facts About 2-Amino-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic Acid
2-Amino-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic acid, often referred to in the context of medicinal chemistry, is a curious compound with intriguing properties and applications. Here are some fascinating insights:
- Chemotherapeutic Agent: This compound is notable for its role as a potential anticancer agent. Its structure suggests a capacity for targeting rapidly dividing cells, a hallmark of many cancer therapies.
- Mechanism of Action: The presence of the bis(2-chloroethyl)amino moiety is relevant, as it is known to form highly reactive species that can lead to DNA cross-linking, thereby inhibiting cell division.
- Structural Complexity: The compound exemplifies a sophisticated design with multiple functional groups, enabling interactions that are vital in pharmacology. The balance between both amine and carboxylic acid groups contributes to its chemical behavior.
- Importance of Chirality: As an amino acid derivative, this compound also exhibits chirality, with implications for its biological interactions and specificity in drug design.
- Research Applications: Ongoing research explores its potential roles not only in cancer treatment but also in addressing other conditions where cellular proliferation is a concern.
In summary, 2-amino-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic acid serves as a prime example of how structure determines function in medicinal chemistry. Understanding its unique properties is crucial for the development of effective therapeutic strategies.
Synonyms
Sarcolysin
Merphalan
531-76-0
Sarcolysinum
Sarcolysine
Sarcolysin [INN]
Sarcoclorin
Sarcolisina
2-amino-3-(4-(bis(2-chloroethyl)amino)phenyl)propanoic acid
DL-Phenylalanine mustard
Sarkolysin
Phenylalanin-lost
Sarcolysine [INN-French]
Sarcolysinum [INN-Latin]
Phenylalanin-lost [German]
Sarcolisina [INN-Spanish]
CCRIS 376
NCI-CO4944
Sarcolysin, dl-
Melphalan dl-form
Mephalan
A960M0G5TP
4-[Bis(2-chloroethyl)amino]phenylalanine
4-(BIS(2-CHLOROETHYL)AMINO)-DL-PHENYLALANINE
AI3-25298
MERPHALAN [IARC]
DL-Phenylalanine, 4-(bis(2-chloroethyl)amino)-
DTXSID9031569
CHEBI:82339
Phenylalanine, 4-(bis(2-chloroethyl)amino)-
NSC 8806
Alanine, 3-(p-(bis(2-chloroethyl)amino)phenyl)-, DL-
2-amino-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic acid
Merfalan
MERPHALAN (IARC)
DL-Sarcolysine
3025 C. B.
DL-Sarcolysin
Sarcolysine (INN-French)
Sarcolysinum (INN-Latin)
Sarcolisina (INN-Spanish)
At-290
2-amino-3-{4-[bis(2-chloroethyl)amino]phenyl}propanoic acid
4-(Bis(2-chloroethyl)amino)phenylalanine
NSC 14210
3-p-(Di(2-chloroethyl)amino) phenyl-L-alanine
3-p-[Di(2-chloroethyl)amino] phenyl-L-alanine
CB-3307
UNII-A960M0G5TP
p-Di(2-chloroethyl)amino-DL-phenylalanine
MFCD00057717
NSC-35051
NSC241286
p-N-Di(chloroethyl)aminophenylalanine
DL-3-(p-(Bis(2-chloroethyl)amino)phenyl)alanine
p-Di-(2-chloraethyl)-amino-DL-phenyl-alanin [German]
Sarcolysin [WHO-DD]
p-Di-(2-chloraethyl)-amino-DL-phenyl-alanin
MERPHALAN [WHO-DD]
D-Phenylalanine mustard base
Lopac0_000793
MLS003899189
SCHEMBL414671
Phenylalanine,4-[bis(2-chloroethyl)amino]-, hydrochloride (1:1)
CHEMBL429405
MELPHALAN DL-FORM [MI]
DTXCID7011569
WLN: QVYZ1R DN2G2G-L
WLN: QVYZ1R DN2G2G -D
HMS3371C10
AAA53176
BCP04106
NCS-8806
NSC35051
STK396207
AKOS003404808
AC-1327
CB 3026
CCG-204877
LP00793
SDCCGSBI-0050770.P002
NCGC00015653-02
NCGC00015653-03
NCGC00015653-04
NCGC00015653-05
NCGC00015653-06
NCGC00015653-07
NCGC00094128-01
NCGC00094128-02
NCGC00094128-03
NCGC00094128-04
NCI60_041947
SMR001456362
DB-042954
p-Bis(.beta.-chloroethyl)aminophenylalanine
EU-0100793
NS00007007
4-[Bis(2-chloroethyl)amino]phenylalanine, L-
C19256
M 2011
SR-01000075983
SR-01000075983-1
Q27155886
2-Amino-3-{4-[bis(2-chloroethyl)amino]phenyl}propionic acid
638-807-0
Solubility of 2-amino-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic acid
The solubility of 2-amino-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic acid, with the chemical formula C13H18Cl2N2O2, is a complex topic due to the intricate structure and functional groups present in the molecule. Generally, solubility can be influenced by several factors, including:
However, it is essential to note that the presence of multiple chlorine atoms may hinder solubility in water, as halogenated compounds often display reduced solubility. In organic solvents, the compound may show improved solubility due to a more compatible chemical environment.
In summary, while 2-amino-3-[4-[bis(2-chloroethyl)amino]phenyl]propanoic acid may exhibit solubility in polar solvents owing to its functional groups, the overall solubility profile is likely to depend on the solvent chosen and the concentrations employed. Understanding these factors is crucial for predicting solubility behaviors in practical applications.