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CAS 128140-12-5

:

leualacin

Description:
Leualacin, with the CAS number 128140-12-5, is a chemical compound that belongs to the class of amino acids. It is characterized by its structure, which includes a branched-chain aliphatic side chain, making it a hydrophobic amino acid. Leualacin is known for its role in protein synthesis and is often studied for its potential applications in nutrition and biochemistry. It is typically found in various natural sources, including proteins in animal and plant tissues. The compound exhibits properties such as solubility in organic solvents and limited solubility in water, which is common among hydrophobic amino acids. Additionally, leualacin may participate in various biochemical pathways, influencing metabolic processes. Its unique structure and properties make it a subject of interest in research related to nutrition, health, and the development of dietary supplements. However, specific applications and effects may vary, and further studies are often required to fully understand its biological significance.
Formula:C31H47N3O7
InChI:InChI=1/C31H47N3O7/c1-19(2)15-23(33)27(39)30(18-35,34(7)29(41)25(37)17-21(5)6)31(26(38)13-14-32,22-11-9-8-10-12-22)28(40)24(36)16-20(3)4/h8-12,18-20,23-25,36-37H,5,13-17,32-33H2,1-4,6-7H3/t23-,24?,25-,30-,31?/m0/s1
Synonyms:
  • Cyclo(beta-alanyl-4-methyl-2-hydroxypentanoylleucyl-4-methyl-2-hydroxypentanoyl-N-methylphenylalanyl)
  • Leualacin
  • Cyclo(beta-alanyl-4-methyl-D-2-hydroxypentanoyl-L-leucyl-4-methyl-L-2-hydroxypentanoyl-N-methyl-L-phenylalanyl)
  • (2S)-N-[(4S,6S)-4-amino-7-(3-aminopropanoyl)-6-formyl-9-hydroxy-2,11-dimethyl-5,8-dioxo-7-phenyldodecan-6-yl]-2-hydroxy-N,4-dimethylpent-4-enamide
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