Interesting facts
Interesting Facts about 4-Amino-3-phenyl-butanoic acid
4-Amino-3-phenyl-butanoic acid, often referred to by its abbreviation, is a fascinating compound in the field of organic chemistry. Here are some noteworthy insights:
- Composition: This compound belongs to the class of amino acids, which are the building blocks of proteins. It features both an amino group and a carboxylic acid, making it crucial for various biochemical processes.
- Biological Relevance: Amino acids play key roles in metabolism and serve as precursors for the synthesis of hormones, neurotransmitters, and other essential molecules. 4-Amino-3-phenyl-butanoic acid may have biological significance in certain metabolic pathways.
- Pharmaceutical Applications: Compounds like 4-amino-3-phenyl-butanoic acid can be explored for their potential therapeutic properties. They may have uses in the development of pharmaceuticals or nutraceuticals due to their structural characteristics.
- Stereochemistry: The compound's stereochemistry can significantly influence its biological activity. Understanding the 3D orientation of its atoms is vital for drug design and function.
As one delves deeper into the chemistry of 4-amino-3-phenyl-butanoic acid, it becomes clear that its study is not only essential due to its structure but also for its potential applications in various scientific fields. "Each amino acid has a story to tell," and this compound is no exception.
Researchers continue to investigate the myriad of ways such compounds can impact health and technology, ensuring that our understanding of this and similar molecules evolves as science progresses.
Synonyms
4-Amino-3-phenylbutanoic acid
Phenibut
1078-21-3
Fenibut
4-Amino-3-phenylbutyric acid
PhGaba
Phenylgamma
phenigamma
Fenigam
Fenigama
Phenigam
Phenylgam
Pgaba
phenygam
Phenigama
beta-Phenyl-gamma-aminobutyric acid
beta-(Aminomethyl)hydrocinnamic acid
beta-Phenyl-gamma-aminobutyrate
beta-(Aminomethyl)benzenepropanoic acid
Benzenepropanoic acid, beta-(aminomethyl)-
EINECS 214-079-6
BRN 2804903
T2M58D6LA8
Dl-4-amino-3-phenylbutanoic acid
PHENIBUT [WHO-DD]
phenyl-GABA
BUTYRIC ACID, 4-AMINO-3-PHENYL-
Benzenepropanoic acid, .beta.-(aminomethyl)-
DTXSID70870838
4-14-00-01723 (Beilstein Handbook Reference)
phenybut
fenibut citrate
4-AMINO-3-PHENYLBUTYRIC ACID [MI]
.BETA.-(AMINOMETHYL)HYDROCINNAMIC ACID
.BETA.-PHENYL-.GAMMA.-AMINOBUTYRIC ACID
.BETA.-(AMINOMETHYL)BENZENEPROPANOIC ACID
citrocard
noophen
(+-)-FENIBUT
(+-)-BETA-PHENYL-GABA
DTXCID80818524
(+-)-.BETA.-PHENYL-GABA
214-079-6
Benzenepropanoic acid, b-(aminomethyl)-
(3R)-4-amino-3-phenylbutanoic acid
(3S)-4-amino-3-phenylbutanoic acid
UNII-T2M58D6LA8
Phenibut; Fenibut
Oprea1_183000
Oprea1_381119
(+/-)-FENIBUT
SCHEMBL340838
3-phenyl-4-aminobutanoic acid
CHEMBL315818
EX-A734
CHEBI:136039
GLXC-20028
HMS3886K05
butanoic acid, 4-amino-3-phenyl-
ALBB-022462
BCP10710
BBL000576
MFCD00456233
s4892
STK182861
(+/-)-.BETA.-PHENYL-GABA
3-amino-2-phenylpropanecarboxylic acid
AKOS000555914
AKOS016347357
CCG-266416
DB13455
GS-3145
3-[3-(Aminomethyl)phenyl]propionic acid
FA130469
NS00018243
D10509
D96082
EN300-110013
Q419559
BRD-A66920069-001-01-3
Z1255487817
Solubility of 4-amino-3-phenyl-butanoic acid
4-amino-3-phenyl-butanoic acid, commonly known as phenylalanine, exhibits intriguing solubility characteristics that are vital for its applications in biochemistry and nutrition.
In terms of its solubility profile:
Overall, as emphasized by its solubility traits, the properties of 4-amino-3-phenyl-butanoic acid make it a versatile compound in both dietary applications and various biochemical environments. Understanding its solubility plays a vital role in maximizing its effectiveness and functionality in scientific and nutritional contexts.