69010-59-9 Usage
Description
H-BETA-ALA-BETA-ALA-BETA-ALA-OH is a synthetic peptide composed of three beta-alanine molecules linked together, with a hydroxyl group at the end. This peptide is widely utilized in research to investigate the interactions between beta-alanine residues and their influence on biological systems. Beta-alanine, a non-proteinogenic amino acid, is crucial for the synthesis of carnosine, a dipeptide that functions as a pH buffer in skeletal muscle tissues. Through the study of H-BETA-ALA-BETA-ALA-BETA-ALA-OH, researchers can explore the potential applications of beta-alanine and related compounds in various physiological processes.
Uses
Used in Research Applications:
H-BETA-ALA-BETA-ALA-BETA-ALA-OH is used as a research tool for studying the interactions between beta-alanine residues and their effects on biological systems. This helps researchers gain insights into the potential applications of beta-alanine and related compounds in various physiological processes.
Used in Pharmaceutical Industry:
H-BETA-ALA-BETA-ALA-BETA-ALA-OH is used as a potential therapeutic agent for conditions related to muscle function and pH regulation. Its role in the synthesis of carnosine, a pH buffer in skeletal muscle tissues, makes it a candidate for the development of treatments targeting muscle fatigue and related disorders.
Used in Sports Nutrition:
H-BETA-ALA-BETA-ALA-BETA-ALA-OH is used as a supplement in sports nutrition to enhance muscle carnosine levels, which can improve exercise performance and reduce muscle fatigue. By increasing carnosine synthesis, this synthetic peptide may help athletes maintain their performance during high-intensity workouts and delay the onset of muscle fatigue.
Used in Cosmetics Industry:
H-BETA-ALA-BETA-ALA-BETA-ALA-OH is used as an ingredient in cosmetic products for its potential skin care benefits. The peptide's role in pH regulation and its antioxidant properties may contribute to the development of skincare products that promote healthy skin and protect against environmental stressors.
Check Digit Verification of cas no
The CAS Registry Mumber 69010-59-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,1 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69010-59:
(7*6)+(6*9)+(5*0)+(4*1)+(3*0)+(2*5)+(1*9)=119
119 % 10 = 9
So 69010-59-9 is a valid CAS Registry Number.
69010-59-9Relevant articles and documents
Structure of the Stacked Cyclic Oligoamides: 1,6-Diaza-2,7-cyclodecadione and 1,5,9-Triaza-2,6,10-cyclododecatrione. A Ring Model of the α-Helix
Tereshko, V.,Monserrat, J. M.,Perez-Folch, J.,Aymami, J.,Fita, I.,Subirana, J. A.
, p. 243 - 251 (2007/10/02)
The structure of two cyclic amides, comprised of methylene and peptide groups, is described.The cyclic amides form parallel columns of stacked hydrogen-bonded rings.The cyclic dimer of butyramide (1,6-diaza-2,7-cyclodecadione) (I), C8H14N2O2, forms monoclinic crystals, space group P21/n, a = 4.874(2), b = 11.714(4), c = 8.088(2) Angstroem, β = 107.3(3) deg, R = 0.125 for 536 observed reflections, I > 3?(I), Z = 2, Dx = 1.28 g cm-3, λ(Cu Kα) = 1.5418 Angstroem,μ = 7.26 cm-1, T = 298 K.Extra peaks were found near the peptide groups, but the R factor could not be reduced by introducing additional parameters to account for disorder.The ten-membered ring skeleton adopts a centrosymmetric crown conformation which is rarely found in other ten-atom rings, but had been described for its isomer 1,5-diaza-6,10-cyclodecadione.A cyclic trimer of β-alanine (1,5,9-triaza-2,6,10-cyclododecatrione) (2), C9H15N3O3, is also studied.It forms trigonal crystals, a = b = 13.74(2), c = 4.82(1) Angstroem, space group R3m, R = 0.060 for 161 observed reflections, I > 2.5?(I), Z = 3, Dx = 1.35 g cm-3, λ(Cu Kα) = 1.5418 Angstroem, μ = 8.16 cm-1, T = 298 K.The 12-atom ring has two conformations which are mirror images and co-exist in the crystal.They appear superimposed in the solved structure.The peptide groups are planar and the organization of the stacked rings is very similar to that of an α-helix.
