M3129
Met-Gly
≥98% (TLC)
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About This Item
Empirical Formula (Hill Notation):
C7H14N2O3S
CAS Number:
Molecular Weight:
206.26
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352202
EC Number:
238-487-9
MDL number:
Product Name
Met-Gly,
assay
≥98% (TLC)
Quality Level
form
powder
color
white
storage temp.
−20°C
SMILES string
OC(CNC([C@@H](N)CCSC)=O)=O
InChI
1S/C7H14N2O3S/c1-13-3-2-5(8)7(12)9-4-6(10)11/h5H,2-4,8H2,1H3,(H,9,12)(H,10,11)/t5-/m0/s1
InChI key
QXOHLNCNYLGICT-YFKPBYRVSA-N
Biochem/physiol Actions
Met-Gly is a dipeptide.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Olga B Morozova et al.
The journal of physical chemistry. B, 113(20), 7398-7406 (2009-05-15)
Time-resolved chemically induced dynamic nuclear polarization (CIDNP) was applied to the investigation of the photo-oxidation of two sulfur containing peptides, glycylmethionine (Gly-Met) and methionylglycine (Met-Gly). It was established that the reaction of Gly-Met with a photosensitizer, triplet 4-carboxybenzophenone, occurs via
Justin Kai-Chi Lau et al.
Journal of the American Society for Mass Spectrometry, 24(4), 543-553 (2013-02-27)
Radical cations [Met-Gly](•+), [Gly-Met](•+), and [Met-Met](•+) have been generated through collision-induced dissociation (CID) of [Cu(II)(CH3CN)2(peptide)](•2+) complexes. Their fragmentation patterns and dissociation mechanisms have been studied both experimentally and theoretically using density functional theory at the UB3LYP/6-311++G(d,p) level. The captodative structure
Urszula Rychlewska et al.
Acta crystallographica. Section C, Crystal structure communications, 66(Pt 2), m51-m54 (2010-02-04)
Crystallographic analysis of a solid solution of two diastereoisomers, i.e. ({(1S,R)-1-carboxy-3-[(R,S)-methylsulfinyl]propyl}aminocarbonyl)methanaminium tetrachloridoaurate(III) and ({(1S,R)-1-carboxy-3-[(S,R)-methylsulfinyl]propyl}aminocarbonyl)methanaminium tetrachloridoaurate(III), (C(7)H(15)N(2)O(4)S)[AuCl(4)], has shown that in the presence of gold(III), the methionine part of the Gly-D,L-Met dipeptide is oxidized to sulfoxide, and no coordination to the