Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

G3502

Sigma-Aldrich

Gly-Tyr

≥98% (TLC)

Synonym(s):

Glycyl-L-tyrosine

Sign Into View Organizational & Contract Pricing
All Photos(1)

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)

Quality Level

200

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

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

Gly-Ala ≥99.0% (NT)

Sigma-Aldrich

50150

Gly-Ala

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
L J Wykes et al.
The American journal of physiology, 267(5 Pt 1), E672-E679 (1994-11-01)
Low tyrosine solubility in total parenteral nutrition (TPN) solutions complicates meeting the aromatic amino acid needs of infants. This study compared the effectiveness of two tyrosine precursors to supply the aromatic amino acid needs of TPN-fed neonatal piglets with a
P Labute et al.
Journal of medicinal chemistry, 44(10), 1483-1490 (2001-05-04)
A method is presented for flexibly aligning small molecules. The method accepts a collection of small molecules with 3D coordinates as input and computes a collection of alignments. Each alignment is given a score, which quantifies the quality of the
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
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
View All Related Papers

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