G3502
Gly-Tyr
≥98% (TLC)
Synonym(s):
Glycyl-L-tyrosine
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About This Item
Linear Formula:
NH2CH2CONHCH(COOH)CH2C6H4OH
CAS Number:
Molecular Weight:
238.24
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
211-525-1
MDL number:
Beilstein/REAXYS Number:
2700715
Product Name
Gly-Tyr,
InChI key
XBGGUPMXALFZOT-VIFPVBQESA-N
InChI
1S/C11H14N2O4/c12-6-10(15)13-9(11(16)17)5-7-1-3-8(14)4-2-7/h1-4,9,14H,5-6,12H2,(H,13,15)(H,16,17)/t9-/m0/s1
SMILES string
NCC(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O
assay
≥98% (TLC)
form
powder
color
white
mp
282 °C
application(s)
peptide synthesis
storage temp.
−20°C
Quality Level
Application
- Elucidating uptake and metabolic fate of dipeptides in CHO cell cultures using (13)C labeling experiments and kinetic modeling: This study delves into the uptake and metabolic processing of dipeptides such as Gly-Tyr in cell cultures, providing insights into their utilization and role in enhancing biopharmaceutical production processes (Naik et al., 2024).
Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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E C Meng et al.
Proteins, 17(3), 266-278 (1993-11-01)
The biological activities of proteins depend on specific molecular recognition and binding. Computational methods for predicting binding modes can facilitate the discovery and design of ligands and yield information on the factors governing complementarity. The DOCK suite of programs has
J D House et al.
Pediatric research, 41(4 Pt 1), 575-583 (1997-04-01)
Tyrosine may be a conditionally indispensable amino acid in the neonate; however, the provision of aromatic amino acids to neonates receiving total parenteral nutrition (TPN) is complicated by the poor solubility of crystalline tyrosine. In the present study, we investigated
S Albers et al.
Clinical science (London, England : 1979), 76(6), 643-648 (1989-06-01)
1. A commercial amino acid solution supplemented with two synthetic dipeptides, L-alanyl-L-glutamine (Ala-Gln) and glycyl-L-tyrosine (Gly-Tyr), or alternatively with isonitrogenous amounts of free alanine and glycine has been continuously infused over 4 h in six apparently healthy volunteers. 2. The
P Stehle et al.
The Journal of nutrition, 126(3), 663-667 (1996-03-01)
Poor solubility hampers the addition of sufficient amounts of free tyrosine to parenteral amino solutions. We investigated the use of a highly soluble synthetic dipeptide, glycyl-L-tyrosine, as a parenteral tyrosine source in 18 male Wistar rats (body weight 180-200 g).
E A Liechty et al.
The Journal of nutrition, 129(6), 1161-1166 (1999-06-04)
The purpose of this study was to determine whether the ovine fetus is capable of increased disposal of an amino acid load; if so, would it respond by increased protein synthesis, amino acid catabolism or both? A further purpose of
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