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Merck

G1002

Gly-Gly

≥99% (titration)

Synonym(s):

Diglycine, Glycyl-glycine

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About This Item

Linear Formula:
NH2CH2CONHCH2COOH
CAS Number:
556-50-3
Molecular Weight:
132.12
UNSPSC Code:
12352209
NACRES:
NA.26
PubChem Substance ID:
24895032
EC Number:
209-127-8
Beilstein/REAXYS Number:
1765223
MDL number:
MFCD00008130

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Product Name

Gly-Gly, ≥99% (titration)

InChI key

YMAWOPBAYDPSLA-UHFFFAOYSA-N

InChI

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

SMILES string

NCC(=O)NCC(O)=O

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

Quality Level

400

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000520993
0000520993
0000517791
0000517791
0000517967

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Methods in Molecular Biology null
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)
THE GLYCYLGLYCINE DIPEPTIDASES OF SKELETAL
MUSCLE AND HUMAN UTERUS*
EMIL L. SMITH
The Journal of Biological Chemistry (1947)
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
Lasse Jenner et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(10), 3812-3816 (2013-02-23)
Here we present an X-ray crystallography structure of the clinically relevant tigecycline antibiotic bound to the 70S ribosome. Our structural and biochemical analysis indicate that the enhanced potency of tigecycline results from a stacking interaction with nucleobase C1054 within the
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Product Information Sheet - G1002

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