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G1377

Sigma-Aldrich

Gly-Gly-Gly

≥98% (TLC)

Synonym(e):

Glycyl-glycyl-glycin, Triglycin

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About This Item

Lineare Formel:
NH2CH2CONHCH2CONHCH2COOH
CAS-Nummer:
556-33-2
Molekulargewicht:
189.17
Beilstein:
1711130
EG-Nummer:
209-122-0
MDL-Nummer:
MFCD00036223
UNSPSC-Code:
12352209
PubChem Substanz-ID:
24895061
NACRES:
NA.26

product name

Gly-Gly-Gly,

Assay

≥98% (TLC)

Form

powder

Farbe

white

Anwendung(en)

peptide synthesis

SMILES String

NCC(=O)NCC(=O)NCC(O)=O

InChI

1S/C6H11N3O4/c7-1-4(10)8-2-5(11)9-3-6(12)13/h1-3,7H2,(H,8,10)(H,9,11)(H,12,13)

InChIKey

XKUKSGPZAADMRA-UHFFFAOYSA-N

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Amino Acid Sequence

Gly-Gly-Gly

Anwendung

Triglycine (Gly-Gly-Gly) is used as a model peptide for studies of physicochemical parameters and molecular associations of small peptides. Triglycine is used as a copper chelator.

Biochem./physiol. Wirkung

Substrat für reproduzierbare Serumproteinmessungen mittels Biuret-Reaktion und für die Untersuchung von Aminotripeptidasen.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Sigma-Aldrich

50200

Gly-Gly

Ala-Ala-Ala-Ala-Ala

Sigma-Aldrich

A5025

Ala-Ala-Ala-Ala-Ala

Gly-Gly BioPerformance Certified, suitable for cell culture, ≥99%

Sigma-Aldrich

G3915

Gly-Gly

Iminodiessigsäure 98%

Sigma-Aldrich

220000

Iminodiessigsäure

Gly-Tyr

Sigma-Aldrich

G3502

Gly-Tyr

Glycylglycin

SAFC

G0674

Glycylglycin

Blake E Ziegler et al.
The journal of physical chemistry. A, 114(44), 11953-11963 (2010-10-26)
Hydrogen/deuterium exchange reactions involving protonated triglycine and deuterated ammonia (ND(3)) have been examined in the gas phase using a Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometer. Ab initio and density functional theory (DFT) calculations have been carried out to
S J Woltman et al.
Analytical chemistry, 67(3), 541-551 (1995-02-01)
The reversible electrochemistry of the Cu(II)/Cu(III) couple was investigated for the copper(II) complexes of triglycine (G3), tetraglycine (G4), and pentaglycine (G5) in alkaline solution using a rotating ring-disk electrode (RRDE). The study was motivated by the need to elucidate electrochemical
Chi-Kit Siu et al.
Journal of the American Society for Mass Spectrometry, 20(6), 996-1005 (2009-03-04)
Fragmentations of tautomers of the alpha-centered radical triglycine radical cation, [GGG(*)](+), [GG(*)G](+), and [G(*)GG](+), are charge-driven, giving b-type ions; these are processes that are facilitated by a mobile proton, as in the fragmentation of protonated triglycine (Rodriquez, C. F. et
Jiyun Shi et al.
Bioconjugate chemistry, 20(4), 750-759 (2009-03-27)
Radiolabeled cyclic RGD (Arg-Gly-Asp) peptides represent a new class of radiotracers with potential for early tumor detection and noninvasive monitoring of tumor metastasis and therapeutic response in cancer patients. This article describes the synthesis of two cyclic RGD peptide dimer
Craig P Schwartz et al.
Proceedings of the National Academy of Sciences of the United States of America, 107(32), 14008-14013 (2010-07-28)
Nitrogen K-edge spectra of aqueous triglycine were measured using liquid microjets, and the effects of Hofmeister-active salts on the spectra were observed. Spectra simulated using density functional theory, sampled from room temperature classical molecular dynamics trajectories, capture all major features
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