40297-96-9 Usage
Uses
Used in Pharmaceutical Research:
H-GLY-LEU-MET-NH2 HCL is used as a research compound for studying the effects of these specific amino acids on protein structure and function. This can help in understanding the role of these amino acids in various biological processes and their potential therapeutic applications.
Used in Peptide-based Drug Development:
H-GLY-LEU-MET-NH2 HCL is used as a building block in the development of peptide-based drugs. H-GLY-LEU-MET-NH2 HCL can be used to create novel peptide sequences with potential therapeutic properties, targeting specific biological pathways or diseases.
Used in Nutritional Supplements:
H-GLY-LEU-MET-NH2 HCL may be used as a dietary supplement to provide the essential amino acids glycine, leucine, and methionine to the body. These amino acids are vital for protein synthesis and various metabolic processes, supporting overall health and well-being.
Used in Cosmetics and Skincare:
H-GLY-LEU-MET-NH2 HCL can be used in cosmetic and skincare products to promote skin health and repair. The amino acids present in the compound may help improve skin elasticity, reduce the appearance of fine lines and wrinkles, and support the skin's natural collagen production.
Used in Food and Beverage Industry:
H-GLY-LEU-MET-NH2 HCL may be used as a flavor enhancer or a nutritional supplement in the food and beverage industry. The amino acids present in the compound can contribute to the taste and nutritional value of various food products, promoting a healthier diet.
Check Digit Verification of cas no
The CAS Registry Mumber 40297-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,9 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40297-96:
(7*4)+(6*0)+(5*2)+(4*9)+(3*7)+(2*9)+(1*6)=119
119 % 10 = 9
So 40297-96-9 is a valid CAS Registry Number.
40297-96-9Relevant academic research and scientific papers
Synthesis of substance-P C-terminal hexapeptide analogues and their biological activity. Analogues with antagonistic activity without containing D-amino acids
Karagiannis,Manopoulou,Poulos,Stavropoulos
, p. 667 - 673 (2007/10/02)
Analogues of the C-terminal hexapeptide of substance P have been synthesized in which each amino-acid residue was replaced by the bulky and strong lipophilic residue Asp(OBzl). The amino-acid residue of other selected places has also been replaced by Glu(
Synthesis of N-Protected Eledoisin (6-11)-hexapeptide Using Proteases as Biocatalysts
Kuhl, Peter,Doering, Guenter,Neubert, Klaus,Jakubke, Hans-Dieter
, p. 423 - 430 (2007/10/02)
Papain and α-chymotrypsin were used for the protease-catalyzed assembly of Boc-protected eledoisin (6-11)-hexapeptide by (2+4)- and (3+3)-segment condensation, respectively, in aqueous-organic solvent systems.As C-components, chemically synthesized Boc-pr
Tritiated peptides. 12. Synthesis and biological activity of [4-3H-Phe8]substance P
Allen,Brundish,Wade,Sandberg,Hanley,Iversen
, p. 1209 - 1213 (2007/10/02)
Substance P has been prepared 3H-labeled at Phe8 by catalytic deiodination of a protected precursor. Synthesis of the precursor was by solid-phase methodology on polydimethylacrylamide resin and by condensation in solution of fragments covering sequences 1-4, 5-7, and 8-11. Free peptide made by each route analyzed satisfactorily and had the same chromatographic characteristics as unlabeled substance P. It was distinguishable from the latter by radioimmunoassay when N and C terminally directed antisera were used and in the ability to cause contractions of isolated guinea pig ileum. Specific radioactivity was 23 Ci/mmol.
