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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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Categorías relacionadas

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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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
Hiromichi Akizawa et al.
Bioconjugate chemistry, 24(2), 291-299 (2013-01-22)
We previously demonstrated that Fab fragments labeled with 3'-[(131)I]iodohippuryl N(ε)-maleoyl-l-lysine ([(131)I]HML) showed low renal radioactivity from early postinjection time, due to a liberation of m-[(131)I]iodohippuric acid by the action of renal brush border enzymes. Since there are lots of enzymes
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
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