(R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid - 26787-75-7

(R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid

Catalog Number: EVT-462326
CAS Number: 26787-75-7
Molecular Formula: C16H15NO5
Molecular Weight: 301.29 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.
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Product Introduction

Description
(R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid, also known as Z-DOPA, is a synthetic amino acid derivative that has been extensively studied for its potential therapeutic applications in various fields of research. This compound is a chiral molecule that has a unique chemical structure, which makes it an interesting target for drug development and other scientific applications.
Applications in Various Fields
(R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid has various applications in medical research, environmental research, and industrial research. In medical research, (R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid has been studied for its potential role in drug development. Clinical trials have shown promising results for the use of this compound in the treatment of Parkinson's disease and other neurological disorders. However, further research is needed to determine the safety and efficacy of this compound in humans. In environmental research, (R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid has been studied for its effects on ecosystems and its role in pollution management. This compound has been shown to have potential environmental impacts, including toxicity to aquatic organisms. In industrial research, (R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid has been used in manufacturing processes to improve product quality and efficiency. Health and safety considerations are important when using this compound in industrial settings.

Properties

CAS Number

26787-75-7

Product Name

(R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid

IUPAC Name

(2R)-2-(4-hydroxyphenyl)-2-(phenylmethoxycarbonylamino)acetic acid

Molecular Formula

C16H15NO5

Molecular Weight

301.29 g/mol

InChI

InChI=1S/C16H15NO5/c18-13-8-6-12(7-9-13)14(15(19)20)17-16(21)22-10-11-4-2-1-3-5-11/h1-9,14,18H,10H2,(H,17,21)(H,19,20)/t14-/m1/s1

InChI Key

CGDQNVNWDDEJPY-CQSZACIVSA-N

SMILES

C1=CC=C(C=C1)COC(=O)NC(C2=CC=C(C=C2)O)C(=O)O

Canonical SMILES

C1=CC=C(C=C1)COC(=O)NC(C2=CC=C(C=C2)O)C(=O)O

Isomeric SMILES

C1=CC=C(C=C1)COC(=O)N[C@H](C2=CC=C(C=C2)O)C(=O)O
Method of Synthesis or Extraction
(R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid can be synthesized using various methods, including chemical synthesis and enzymatic synthesis. Chemical synthesis involves the use of chemical reactions to produce the compound, while enzymatic synthesis involves the use of enzymes to catalyze the reaction. The efficiency and yield of each method depend on various factors, such as the starting materials, reaction conditions, and purification methods. Chemical synthesis methods have been reported to have higher yields and efficiency compared to enzymatic synthesis methods. However, enzymatic synthesis methods are considered to be more environmentally friendly and safer than chemical synthesis methods.
Chemical Structure and Biological Activity
(R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid has a unique chemical structure that consists of a carboxylic acid, an amine, and a phenolic group. This compound has been shown to have various biological activities, including anti-inflammatory, antioxidant, and neuroprotective effects. The mechanism of action of (R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid involves the inhibition of the enzyme catechol-O-methyltransferase (COMT), which is involved in the metabolism of dopamine and other catecholamines. This inhibition leads to an increase in the levels of dopamine and other catecholamines in the brain, which can have various therapeutic effects.
Biological Effects
(R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid has been shown to have various biological effects on cell function and signal transduction. This compound has been reported to modulate the activity of various signaling pathways, including the MAPK/ERK pathway and the PI3K/Akt pathway. (R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid has also been shown to have potential therapeutic and toxic effects. This compound has been studied for its potential use in the treatment of various diseases, including Parkinson's disease, Alzheimer's disease, and cancer. However, (R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid has also been shown to have potential toxic effects, including hepatotoxicity and nephrotoxicity.
Future Perspectives and Challenges
(R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid has promising future prospects in the application in scientific research. However, there are current limitations in the use and study of this compound, including the lack of understanding of its long-term effects and potential toxicity. Possible solutions and improvements include the development of safer and more efficient synthesis methods and the identification of new therapeutic targets for this compound. Future trends and prospects in the application of (R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid in scientific research include the development of new drugs and therapies for various diseases and the exploration of its potential applications in other fields of research, such as environmental and industrial research.
Conclusion:
(R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid is a synthetic amino acid derivative that has been extensively studied for its potential therapeutic applications in various fields of research. This compound has a unique chemical structure and has been shown to have various biological activities and effects on cell function and signal transduction. (R)-2-(Carbobenzoxy)amino-2-(4-hydroxyphenyl)acetic Acid has various applications in medical research, environmental research, and industrial research. However, there are current limitations in the use and study of this compound, and further research is needed to determine its safety and efficacy in humans.

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