2189-26-6 Usage
Uses
Used in Dietary Supplements:
Glycyl-DL-Tryptophan is used as a dietary supplement to provide the essential amino acid tryptophan, which the body cannot produce on its own and must be obtained through dietary sources. It supports protein synthesis and various physiological functions.
Used in Pharmaceutical Formulations:
Glycyl-DL-Tryptophan is used in pharmaceutical formulations for its potential health benefits and therapeutic applications. The combination of tryptophan and glycine may have synergistic effects that contribute to overall health and well-being.
Used in Nutritional Products:
Glycyl-DL-Tryptophan is used in nutritional products to enhance the amino acid profile and support protein synthesis. Its presence in these products may contribute to improved health and well-being.
Used in Research and Development:
Glycyl-DL-Tryptophan is used in research and development for its potential therapeutic applications. The synergistic effects of tryptophan and glycine in GLYCYL-DL-TRYPTOPHAN may offer new insights into the development of treatments for various health conditions.
Used in Metabolic Processes:
Glycyl-DL-Tryptophan is used in metabolic processes, particularly in the synthesis of proteins and neurotransmission. The presence of both essential and non-essential amino acids in GLYCYL-DL-TRYPTOPHAN may contribute to the efficient functioning of these processes.
Check Digit Verification of cas no
The CAS Registry Mumber 2189-26-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,8 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2189-26:
(6*2)+(5*1)+(4*8)+(3*9)+(2*2)+(1*6)=86
86 % 10 = 6
So 2189-26-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H15N3O3/c14-6-12(17)16-11(13(18)19)5-8-7-15-10-4-2-1-3-9(8)10/h1-4,7,11,15H,5-6,14H2,(H,16,17)(H,18,19)
2189-26-6Relevant academic research and scientific papers
PROTECTION OF THE TRYPTOPHAN INDOLE RING IN PEPTIDE SYNTHESIS. USE OF A NEW DERIVATIVE, Nin-2,2,2-TRICHLOROETHOXYCARBONYLTRYPTOPHAN
Kiso, Yoshiaki,Inai, Masatoshi,Kitagawa, Kouki,Akita, Tadashi
, p. 739 - 742 (2007/10/02)
The 2,2,2-trichloroethoxycarbonyl (Troc) group attached at the Nin function of tryptophan by acylation with Troc-Cl in the presence of a catalytic amount of tetra-n-butylammonium hydrogensulfate can be quantitatively removed either by cadmium dust in acetic acid or under basic conditions, e. g., hydrazine hydrate and NaOH, but is resistant to strong acidic conditions.
