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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Product Name: Cyclo(Ala-Tyr) Visit Supplier Webpage Request for quotationCAS: 21754-26-7
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tech@medchemexpress.com
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Product Name: Cyclo(Ala-Tyr) Visit Supplier Webpage Request for quotation
CAS: 21754-26-7
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CAS: 21754-26-7
Tel: 18301782025
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View History
Cyclo(Ala-Tyr)
N4-乙酰胞嘧啶核苷
1,2,3-Propanetriol, 2-methyl-, 1-(4-methylbenzenesulfonate), (S)- (9CI)
2一乙酰氧基一5一甲氧基一6一甲基3-[(Z-10-十五烯基)-1,4-苯醌
2-hydroxyethyl dihydrogenphosphate
N-(2-碘苯基)乙酰胺
1-乙酰金刚烷胺
1-(Indol-3-yl)Butan-3-One
BETA-(AMINOMETHYL)-4-CHLOROBENZENEETHANESULFONIC ACID
洛索洛芬EP杂质K
N4-乙酰胞嘧啶核苷
1,2,3-Propanetriol, 2-methyl-, 1-(4-methylbenzenesulfonate), (S)- (9CI)
2一乙酰氧基一5一甲氧基一6一甲基3-[(Z-10-十五烯基)-1,4-苯醌
2-hydroxyethyl dihydrogenphosphate
N-(2-碘苯基)乙酰胺
1-乙酰金刚烷胺
1-(Indol-3-yl)Butan-3-One
BETA-(AMINOMETHYL)-4-CHLOROBENZENEETHANESULFONIC ACID
洛索洛芬EP杂质K