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G3502

Sigma-Aldrich

Gly-Tyr

≥98% (TLC)

Synonym(s):

Glycyl-L-tyrosine

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About This Item

Linear Formula:
NH2CH2CONHCH(COOH)CH2C6H4OH
CAS Number:
658-79-7
Molecular Weight:
238.24
Beilstein:
2700715
EC Number:
211-525-1
MDL number:
MFCD00008126
UNSPSC Code:
12352209
PubChem Substance ID:
24895127
NACRES:
NA.26

product name

Gly-Tyr,

Assay

≥98% (TLC)

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

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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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Gly-Ala ≥99.0% (NT)

Sigma-Aldrich

50150

Gly-Ala

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 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
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 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
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