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G1002

Sigma-Aldrich

Gly-Gly

≥99% (titration)

Sinónimos:

Diglycine, Glycyl-glycine

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About This Item

Fórmula lineal:
NH2CH2CONHCH2COOH
Número de CAS:
556-50-3
Peso molecular:
132.12
Beilstein/REAXYS Number:
1765223
EC Number:
209-127-8
MDL number:
MFCD00008130
UNSPSC Code:
12352209
PubChem Substance ID:
24895032
NACRES:
NA.26

assay

≥99% (titration)

form

powder

color

white

useful pH range

7.5-8.9

pKa (25 °C)

8.2

mp

262-264 °C

application(s)

diagnostic assay manufacturing

SMILES string

NCC(=O)NCC(O)=O

InChI

1S/C4H8N2O3/c5-1-3(7)6-2-4(8)9/h1-2,5H2,(H,6,7)(H,8,9)

InChI key

YMAWOPBAYDPSLA-UHFFFAOYSA-N

Gene Information

human ... SLC15A1(6564)

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Application

Gly-Gly has been used as a buffer for the measurement of glucose-6-phosphate dehydrogenase (G6PDH) activity and as a component of luciferase assay buffer.

Biochem/physiol Actions

Gly-Gly or diglycine is the simplest dipeptide. It may possess proteolytic properties. Gly-gly is hydrolyzed by glycylglycine dipeptidase.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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-Ala

Sigma-Aldrich

A9502

Ala-Ala

Triglycine United States Pharmacopeia (USP) Reference Standard

USP

1686386

Triglycine

Primary Epithelial Cell Models for Cystic Fibrosis Research
Scott H. Randell
Methods in Molecular Biology null
THE GLYCYLGLYCINE DIPEPTIDASES OF SKELETAL
MUSCLE AND HUMAN UTERUS*
EMIL L. SMITH
The Journal of Biological Chemistry (1947)
Open questions in origin of life: experimental studies on the origin of nucleic acids and proteins with specific and functional sequences by a chemical synthetic biology approach
Katarzyna A
Computational and structural biotechnology journal, 9, e201402004-e201402004 (2014)
Zheng Ma et al.
Antimicrobial agents and chemotherapy, 53(7), 2857-2864 (2009-04-22)
Nephrotoxicity is an important limitation to the clinical use of colistin against Pseudomonas aeruginosa and other gram-negative pathogens. Previous work reported net tubular reabsorption of colistin by the kidney in vivo, but there is no knowledge of its disposition within
P B Armentrout et al.
Journal of the American Society for Mass Spectrometry, 23(4), 621-631 (2011-09-29)
We present a full computational description of the fragmentation reactions of protonated diglycine (H(+)GG). Relaxed potential energy surface scans performed at B3LYP/6-31 G(d) or B3LYP/6-311 + G(d,p) levels are used to map the reaction coordinate surfaces and identify the transition states (TSs) and
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Protocolos

Enzymatic Assay of Glucose-6-Phosphate Dehydrogenase (EC 1.1.1.49)

To measure glucose-6-phosphate dehydrogenase activity, beta-nicotinamide adenine dinucleotide phosphate is used in a spectrophotometric rate determination assay at 340 nm.

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