Interesting facts
Interesting Facts about 2-amino-3-(3-hydroxyphenyl)-2-methyl-propanoic acid
2-amino-3-(3-hydroxyphenyl)-2-methyl-propanoic acid, often referred to as a derivative of the well-known amino acid, is fascinating for several reasons:
- Role in Biochemistry: This compound plays a crucial role in various biochemical processes, particularly in metabolism and protein synthesis.
- Potential Medicinal Uses: Due to its structural similarity to amino acids, it may exhibit properties that can be exploited for therapeutic applications, such as in the treatment of neurological disorders.
- Phenolic Connection: The presence of the hydroxyphenyl group introduces unique electron-donating properties, which can affect the compound's reactivity and interactions with biological systems.
- Steric Hindrance: The methyl group attached to the central carbon increases steric hindrance, affecting how this compound interacts with enzymes and receptors, which is a critical aspect in drug design.
- Research Significance: Ongoing research into this compound may unveil new insights into amino acid derivatives and their implications in fields such as medicinal chemistry, pharmacology, and nutrition.
As you delve into the study of this compound, keep in mind the intricacies of its structure and the myriad of ways it can influence biological systems. In the words of a famous chemist, "Chemistry is the central science" - bridging gaps and opening doors to understanding life's processes.
Whether you are a chemistry student or a seasoned researcher, exploring compounds like 2-amino-3-(3-hydroxyphenyl)-2-methyl-propanoic acid will deepen your appreciation for the complexity and beauty of chemical interactions!
Synonyms
alpha-Methyl-m-tyrosine
305-96-4
dl-alpha-Methyl-m-tyrosine
a-mmt
62-25-9
alpha-Methyl-D,L-m-tyrosine
A-METHYL-D,L-M-TYROSINE
2-amino-3-(3-hydroxyphenyl)-2-methylpropanoic acid
alpha-Methyl-DL-m-tyrosine
DL-.alpha.-Methyl-m-tyrosine
Phenylalanine, 3-hydroxy-.alpha.-methyl-
EINECS 206-172-5
9UL7R46488
AI3-62543
DTXSID20883357
.ALPHA.-METHYL-M-TYROSINE
NSC 92520
.ALPHA.-METHYL-D,L-M-TYROSINE
.ALPHA.-METHYL-M-TYROSINE [MI]
Phenylalanine, 3-hydroxy-alpha-methyl-
|A-methyl-m-tyrosine
AC1L1CXX
UNII-9UL7R46488
3-Hydroxy-?-methylphenylalanine; ?-Methyl-m-tyrosine; 3-Hydroxy-?-methyl-3-
DL-?-Methyl-m-tyrosine
Maybridge4_003461
alpha-methyl-meta-tyrosine
?-Methyl-D,L-m-tyrosine
?-MMT
SCHEMBL586073
alpha -Methyl-D,L-m-tyrosine
CHEBI:10303
CAHPJJJZLQXPKS-UHFFFAOYSA-N
DTXCID701022894
NSC92520
NSC-92520
(.+-.)-.alpha.-Methyl-m-tyrosine
AKOS006275061
3-Hydroxy-alpha-methyl-3-phenylalanine
CCG-256347
FM66494
NCGC00175819-01
DL-.alpha.-Methyl-3-hydroxyphenylalanine
DB-054111
NS00042247
DL-ALPHA-METHYL-M-TYROSINE MONOHYDRATE
DL-Phenylalanine, 3-hydroxy-.alpha.-methyl-
2-amino-3-(3-hydroxyphenyl)-2-methyl-propanoic acid
Q27108613
Solubility of 2-amino-3-(3-hydroxyphenyl)-2-methyl-propanoic acid (C9H11NO2)
The solubility of 2-amino-3-(3-hydroxyphenyl)-2-methyl-propanoic acid can be characterized by several key factors:
In summary, the solubility of 2-amino-3-(3-hydroxyphenyl)-2-methyl-propanoic acid in water is expected to be relatively high due to its polar nature and ability to form hydrogen bonds. This property makes it highly relevant for biological and chemical applications.