G3502
Gly-Tyr
≥98% (TLC)
Synonym(s):
Glycyl-L-tyrosine
Sign Into View Organizational & Contract Pricing
Select a Size
About This Item
Linear Formula:
NH2CH2CONHCH(COOH)CH2C6H4OH
CAS Number:
Molecular Weight:
238.24
Beilstein:
2700715
EC Number:
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26
Product Name
Gly-Tyr,
Assay
≥98% (TLC)
Quality Level
form
powder
color
white
mp
282 °C
application(s)
peptide synthesis
storage temp.
−20°C
SMILES string
NCC(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O
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
InChI key
XBGGUPMXALFZOT-VIFPVBQESA-N
Looking for similar products? Visit Product Comparison Guide
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 Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
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 M Booth et al.
The journal of physical chemistry. B, 110(25), 12419-12426 (2006-06-28)
Voltammetric techniques have been introduced to monitor the formation of gold nanoparticles produced via the reaction of the amino acid glycyl-L-tyrosine with Au(III) (bromoaurate) in 0.05 M KOH conditions. The alkaline conditions facilitate amino acid binding to Au(III), inhibit the
S A Roberts et al.
Pediatric research, 49(1), 111-119 (2001-01-03)
Although tyrosine is considered indispensable during the neonatal period, its poor solubility has limited its inclusion in parenteral amino acid solutions to less than 1% of total amino acids. Dipeptides of tyrosine are highly soluble, have been shown to be
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).
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service