G1627
Gly-His
powder
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About This Item
Empirical Formula (Hill Notation):
C8H12N4O3
CAS Number:
Molecular Weight:
212.21
UNSPSC Code:
12352202
PubChem Substance ID:
NACRES:
NA.26
MDL number:
Product Name
Gly-His,
SMILES string
NCC(=O)NC(Cc1cnc[nH]1)C(O)=O
InChI
1S/C8H12N4O3/c9-2-7(13)12-6(8(14)15)1-5-3-10-4-11-5/h3-4,6H,1-2,9H2,(H,10,11)(H,12,13)(H,14,15)
InChI key
YIWFXZNIBQBFHR-UHFFFAOYSA-N
form
powder
color
white
storage temp.
−20°C
Quality Level
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Giulio Vistoli et al.
Biochemical and biophysical research communications, 492(3), 487-492 (2017-08-24)
The study combines HPLC-based with MS-based competitive analyses to evaluate the quenching activity of a set of carnosine derivatives towards methylglyoxal (MGO) and malondialdehyde (MDA) chosen as representative of α- and β-dicarbonyls, respectively. The obtained results underline that these derivatives
Javiera Cortés-Ríos et al.
Analytical biochemistry, 608, 113904-113904 (2020-08-18)
Amongst the available methodologies for protein determination, the bicinchoninic acid (BCA) assay highlights for its simplicity, sensitivity, repeatability and reproducibility. Nevertheless, in spite that the general principle behind this methodology is known, there are still unanswered questions regarding the chemistry
Michael S Kostelansky et al.
Biochemistry, 43(9), 2475-2483 (2004-03-03)
Structural analysis of recombinant fibrinogen fragment D revealed that the calcium-binding site (beta2-site) composed of residues BbetaAsp261, BbetaAsp398, BbetaGly263, and gammaGlu132 is modulated by the "B:b" interaction. To determine the beta2-site's role in polymerization, we engineered variant fibrinogen gammaE132A in
E Matczak-Jon et al.
Journal of inorganic biochemistry, 12(2), 143-156 (1980-04-01)
1H and 13C nmr studies on the Pd(II)Gly-His complex interaction with cytidine and GMP have shown that the nucleoside binds the palladium complex via N3 nitrogen and the nucleotide binds that complex via N7 nitrogen. The analysis of the Cyd
Giampiero De Sanctis et al.
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 11(2), 153-167 (2005-12-13)
The pH dependence of redox properties, spectroscopic features and CO binding kinetics for the chelated protohemin-6(7)-L-histidine methyl ester (heme-H) and the chelated protohemin-6(7)-glycyl-L-histidine methyl ester (heme-GH) systems has been investigated between pH 2.0 and 12.0. The two heme systems appear
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