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Merck
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Key Documents

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G3502

Sigma-Aldrich

Gly-Tyr

≥98% (TLC)

Sinónimos:

Glycyl-L-tyrosine

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About This Item

Fórmula lineal:
NH2CH2CONHCH(COOH)CH2C6H4OH
Número de CAS:
658-79-7
Peso molecular:
238.24
Beilstein/REAXYS Number:
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

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Ala-Leu

Sigma-Aldrich

A1878

Ala-Leu

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
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 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).
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 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
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