Interesting facts
Interesting Facts about 2-amino-3-(4-hydroxy-3,5-diiodo-phenyl)propanoic acid
2-amino-3-(4-hydroxy-3,5-diiodo-phenyl)propanoic acid, often referred to in scientific circles for its complex structure, is a fascinating compound with several noteworthy aspects:
- Structural Complexity: This compound contains multiple functional groups, including an amino group, hydroxyl group, and iodine substituents. This multi-functionality contributes to its diverse chemical behavior and reactivity.
- Halogenated Aromatic Compound: The presence of iodine atoms introduces unique properties, such as increased molecular weight and potential for novel interactions in biochemical systems. The halogen substituents can significantly alter the activity of the parent molecule.
- Biological Significance: Compounds similar to this structure are known to play roles in biological systems, particularly in the context of metabolism and signaling. They may serve as models for studying various biochemical pathways and interactions.
- Potential Therapeutic Applications: Research has suggested that derivatives of amino acids substituted with halogens could exhibit interesting pharmacological activities, paving the way for new drug discoveries.
- Environmental Impact: The iodine content may also contribute to unique environmental behaviors, particularly in marine ecosystems, where halogenated compounds can affect the bioavailability and toxicity of certain drugs and pollutants.
To quote a well-known chemist, "The beauty of chemistry lies in the intricacies of molecular interactions." Understanding compounds like 2-amino-3-(4-hydroxy-3,5-diiodo-phenyl)propanoic acid is essential for advancing our knowledge of both organic chemistry and its applications in science and medicine.
Synonyms
66-02-4
2-amino-3-(4-hydroxy-3,5-diiodophenyl)propanoic acid
3,5-Diiodo-DL-tyrosine
Jodgorgon
Cemiod
Itir
Iodogorgoic acid
Iodogorgonic acid
Diidotyrosine
Jodgorgosaeure
Apothyrin
Flaianina
Agontan
Dityrin
Tyrosine, 3,5-diiodo-
Gorgoic acid, diiodo-
Gorgonic acid, diiodo-
DL-3,5-Diiodotyrosine
3,5-Diiodo-4-hydroxyphenylalanine
2-Amino-3-(4-hydroxy-3,5-diiodophenyl)-propanoic acid
C9H9I2NO3
ST90Q60YF3
NSC4143
NSC-97936
620-59-7
.beta.-(4-Hydroxy-3,5-diiodophenyl)alanine
NSC 208959
Diiodotyrosine, dl-
DIT (VAN)
NSC-208959
3,5-Diiodotyrosine (VAN)
3,5-diiodotyrosine dl-form
3,5-Diiod-L-tyrosin
EINECS 200-620-3
Tyrosine, 3,5-diiodo-, labeled with carbon-14
BRN 2218690
UNII-ST90Q60YF3
beta-(4-Hydroxy-3,5-diiodophenyl)alanine
NSC-4143
MFCD00237693
NSC208959
Acid, iodogorgoic
3,5-Dijodtyrosin
EINECS 210-643-0
MFCD00063076
Tyrosine,5-diiodo-
3953-13-7
beta-(3,5-Diiod-4-hydroxyphenyl)alanin
DL-Tyrosine,5-diiodo-
DIIODO-L-TRYOSINE
(S)-3-(4-Hydroxy-3,5-diiodphenyl)alanin
Tyrosine,5-diiodo-, L-
TRYOSINE,5-DIIODO-
Tyrosine,5-diiodo-, DL-
CBDivE_002920
2-14-00-00384 (Beilstein Handbook Reference)
SCHEMBL147578
(S)-3-(4-Hydroxy-3,5-diiodphenyl)alanin [IUPAC]
2-Amino-3-(4-hydroxy-3,5-diiodophenyl)propanoicacid
DIIODOTYROSINE [WHO-DD]
2-amino-3-(4-hydroxy-3,5-diiodo-phenyl)propanoic acid
CHEMBL2003070
L-2-Amino-3-(3,5-diiod-4-hydroxyphenyl)propionsaeure
DTXSID50110067
NYPYHUZRZVSYKL-UHFFFAOYSA-N
diiodotyrosine (no stereo defined)
HMS3370A04
(2S)-2-ammonio-3-(3,5-diiodo-4-oxidophenyl)propanoate
NSC97936
3,5-diiodo-L-Tyrosinic acid(1-)
NSC 97936
AKOS015998813
HY-W052493
3,5-DIIODOTYROSINE DL-FORM [MI]
DS-18174
NCI60_001756
SY041404
DB-183018
CS-0045361
NS00114171
EN300-178305
Q28091398
Z90343194
F3284-0277
(2S)-2-ammonio-3-(3,5-diiodo-4-Oxidophenyl)propanoic acid
2-Amino-3-(4-hydroxy-3,5-diiodophenyl)propanoic acid (H-DL-Tyr(3,5-diI)-OH)
Solubility of 2-amino-3-(4-hydroxy-3,5-diiodo-phenyl)propanoic acid
The solubility of the compound 2-amino-3-(4-hydroxy-3,5-diiodo-phenyl)propanoic acid, with the chemical formula C15H11I2NO4, is influenced by several key factors, including its molecular structure and the presence of functional groups.
Understanding solubility can often be summarized by considering:
According to the principle of “like dissolves like”, compounds with similar polarities will tend to be soluble in each other. Therefore:
In conclusion, while the compound is likely soluble in polar solvents, its precise solubility profile would require experimental data to determine accurately, considering the complexity introduced by its molecular structure and the interactions of its functional groups.