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G3502

Sigma-Aldrich

Gly-Tyr

≥98% (TLC)

Synonym(e):

Glycyl-L-tyrosin

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About This Item

Lineare Formel:
NH2CH2CONHCH(COOH)CH2C6H4OH
CAS-Nummer:
658-79-7
Molekulargewicht:
238.24
Beilstein:
2700715
EG-Nummer:
211-525-1
MDL-Nummer:
MFCD00008126
UNSPSC-Code:
12352209
PubChem Substanz-ID:
24895127
NACRES:
NA.26

product name

Gly-Tyr,

Assay

≥98% (TLC)

Form

powder

Farbe

white

mp (Schmelzpunkt)

282 °C

Anwendung(en)

peptide synthesis

Lagertemp.

−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

InChIKey

XBGGUPMXALFZOT-VIFPVBQESA-N

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Anwendung


  • 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).

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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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
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
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