Gly-Ser-OH (CAS 7361-43-5)
QUICK LINKS
Gly-Ser-OH, a derivative of amino acids glycine and L-serine, has garnered significant attention in scientific research due to its potential applications across various fields. This compound serves as a valuable biochemical reagent, plays a role as a structural component of proteins. The applications of Gly-Ser-OH in scientific research span a wide range. It has found utility as a biochemical reagent in studying enzymatic reactions, as a fundamental building block in protein structures. Furthermore, Gly-Ser-OH has contributed to the exploration of metabolic pathways. Gly-Ser-OH has demonstrated inhibitory effects on specific enzymes involved in metabolic pathways, potentially functioning as an enzyme inhibitor. Moreover, it has been proposed to act as a structural component by binding to certain proteins. Believed to block the activity of specific enzymes in metabolic pathways, Gly-Ser-OH holds promise as an enzyme inhibitor. Furthermore, it has been suggested that its interaction with certain proteins may contribute to its role as a structural component.
Gly-Ser-OH (CAS 7361-43-5) References
- What is the best crystal size for collection of X-ray data? Refinement of the structure of glycyl-L-serine based on data from a very large crystal. | Görbitz, CH. 1999. Acta Crystallogr B. 55: 1090-1098. PMID: 10927450
- Peptidases in human blood. IV. The hydrolysis of glycyl-L-leucine and other dipeptides by leucocytes. | FLEISHER, GA. 1956. Arch Biochem Biophys. 61: 119-27. PMID: 13292946
- Metabolism of glycine and serine in Escherichia coli. | SIMMONDS, S. and MILLER, DA. 1957. J Bacteriol. 74: 775-83. PMID: 13502304
- Gas-phase basicities of serine and dipeptides of serine and glycine. | McKieman, JW., et al. 1994. J Am Soc Mass Spectrom. 5: 718-23. PMID: 24221998
- Serine-borate complex as a transition-state inhibitor of gamma-glutamyl transpeptidase. | Tate, SS. and Meister, A. 1978. Proc Natl Acad Sci U S A. 75: 4806-9. PMID: 33382
- Kinetic studies on the alkali-catalyzed hydrolysis and epimerization of model alkyl and hydroxyalkyl di- and tripeptides. | Noll, BW., et al. 1974. Biochemistry. 13: 5164-9. PMID: 4433513
- The irreversible redox rearrangment of cobalt oxygen complexes of dipeptides. | Harris, WR., et al. 1977. J Am Chem Soc. 99: 2958-63. PMID: 850044
- Oxygenation equilibriums of cobalt(II) complexes of amino acids and dipeptides | Wesley R. Harris, George McLendon, and Arthur E. Martell. 1976. J. Am. Chem. Soc. 98, 26: 8378–8381.
- Studies on transition-metal–peptide complexes. Part 6. Influence of side-chain donor group on the equilibrium and thermodynamics of binary and ternary copper(II)–dipeptide complexes | Arthur Gergely and Etelka Farkas. 1982. J. Chem. Soc., Dalton Trans. 2: 381-386.
- Effects of side-chain donor groups on deprotonation of peptide amide in copper(II) complexes at high pH | E Farkas, T Kiss. 1989. Polyhedron. 8 (20): 2463-2467.
- An ESR study of the copper(II)–glycyl-l-serine and copper(II)–l-seryl-glycine systems by the simultaneous analysis of multi-component isotropic spectra. Formation constants and coordination modes | T Szabó-Plánka, Z Árkosi, A Rockenbauer, L Korecz. 2001. Polyhedron. 20 (9–10): 995-1003.
- Copper(II) complexes with hydroxyl-containing dipeptides glycyl- L -serine and L -seryl- L -tyrosine | Tsonko Kolev, et al. 2008. Journal of Coordination Chemistry. 61, 12: 1897-1905.
- The enthalpies of solution of some dipeptides in aqueous urea mixtures at T = 298.15 K | B Pałecz, S Belica, B Nowicka. 2009. The Journal of Chemical Thermodynamics. 41, 8: 923-925.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Gly-Ser-OH, 1 g | sc-479097 | 1 g | $102.00 | |||
Gly-Ser-OH, 5 g | sc-479097A | 5 g | $342.00 |