Cyclo(Ala-Tyr)
Cyclo(Ala-Tyr)
CAS: 21754-26-7
Molecular Formula: C12H14N2O3
Cyclo(Ala-Tyr) - Names and Identifiers
| Name | Cyclo(Ala-Tyr) |
| Synonyms | Cyclo(Ala-Tyr) cyclo(Tyr-Ala) 2,5-Piperazinedione, 3-[(4-hydroxyphenyl)methyl]-6-methyl-, (3S,6S)- |
| CAS | 21754-26-7 |
Cyclo(Ala-Tyr) - Physico-chemical Properties
| Molecular Formula | C12H14N2O3 |
| Molar Mass | 234.25 |
| Density | 1.244±0.06 g/cm3(Predicted) |
| Boling Point | 599.6±40.0 °C(Predicted) |
| pKa | 9.90±0.15(Predicted) |
| Storage Condition | 2-8℃ |
Cyclo(Ala-Tyr) - Introduction
Cyclo(Ala-Tyr)(cycloalanyl-tyrosyl) is an amino acid dipeptide consisting of alanyl (Ala) and tyrosyl (Tyr). Its structure is characterized by the formation of a ring structure between alanine residues and tyrosine residues.
Cyclo(Ala-Tyr) has important physiological functions in organisms and can participate in a variety of biochemical processes, including protein synthesis, signal transduction and metabolism. It has antioxidant, anti-aging, anti-inflammatory and other activities, so it has a wide range of applications in the field of drug research and beauty.
A common method for preparing Cyclo(Ala-Tyr) is through chemical synthesis. Generally, the strategy of amino acid protecting group is to first protect the side chain Group of the reactant, then connect alanine and tyrosine into a ring structure through hydrazide coupling and cyclization reaction, and finally remove the protecting group to obtain the target product.
Regarding safety information, Cyclo(Ala-Tyr), as a natural amino acid dipeptide, often exists in organisms and has good biocompatibility and biological safety. However, further research and evaluation are needed for specific toxicity and hazards, such as following relevant laboratory practices and safe operating procedures.
Cyclo(Ala-Tyr) has important physiological functions in organisms and can participate in a variety of biochemical processes, including protein synthesis, signal transduction and metabolism. It has antioxidant, anti-aging, anti-inflammatory and other activities, so it has a wide range of applications in the field of drug research and beauty.
A common method for preparing Cyclo(Ala-Tyr) is through chemical synthesis. Generally, the strategy of amino acid protecting group is to first protect the side chain Group of the reactant, then connect alanine and tyrosine into a ring structure through hydrazide coupling and cyclization reaction, and finally remove the protecting group to obtain the target product.
Regarding safety information, Cyclo(Ala-Tyr), as a natural amino acid dipeptide, often exists in organisms and has good biocompatibility and biological safety. However, further research and evaluation are needed for specific toxicity and hazards, such as following relevant laboratory practices and safe operating procedures.
Last Update：2024-04-09 20:45:29
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CAS: 21754-26-7
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CAS: 21754-26-7
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Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
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