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Details

Stereochemistry ABSOLUTE
Molecular Formula C7H14N2O3S
Molecular Weight 206.263
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLYCYLMETHIONINE

SMILES

CSCC[C@H](NC(=O)CN)C(O)=O

InChI

InChIKey=PFMUCCYYAAFKTH-YFKPBYRVSA-N
InChI=1S/C7H14N2O3S/c1-13-3-2-5(7(11)12)9-6(10)4-8/h5H,2-4,8H2,1H3,(H,9,10)(H,11,12)/t5-/m0/s1

HIDE SMILES / InChI

Molecular Formula C7H14N2O3S
Molecular Weight 206.263
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Photo-CIDNP study of transient radicals of Met-Gly and Gly-Met peptides in aqueous solution at variable pH.
2009-05-21
Kinetics and mechanism of the substitution reactions of [PtCl(bpma)]+, [PtCl(gly-met-S,N,N)] and their aqua analogues with L-methionine, glutathione and 5'-GMP.
2007-11
The membrane-associated lipoprotein-9 GmpC from Staphylococcus aureus binds the dipeptide GlyMet via side chain interactions.
2004-12-28
Sites of hydroxyl radical reaction with amino acids identified by (2)H NMR detection of induced (1)H/(2)H exchange.
2001-02-14
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:52:22 GMT 2025
Edited
by admin
on Mon Mar 31 21:52:22 GMT 2025
Record UNII
0H4L5K3198
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-88866
Preferred Name English
GLYCYLMETHIONINE
Systematic Name English
L-METHIONINE, GLYCYL-
Systematic Name English
N-GLYCYLMETHIONINE
Systematic Name English
N-GLYCYLMETHIONINE, L-
Common Name English
L-METHIONINE, N-GLYCYL-
Systematic Name English
GLYCYL-L-METHIONINE
Systematic Name English
METHIONINE, N-GLYCYL-, L-
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
209-076-1
Created by admin on Mon Mar 31 21:52:22 GMT 2025 , Edited by admin on Mon Mar 31 21:52:22 GMT 2025
PRIMARY
CAS
554-94-9
Created by admin on Mon Mar 31 21:52:22 GMT 2025 , Edited by admin on Mon Mar 31 21:52:22 GMT 2025
PRIMARY
CHEBI
74120
Created by admin on Mon Mar 31 21:52:22 GMT 2025 , Edited by admin on Mon Mar 31 21:52:22 GMT 2025
PRIMARY
PUBCHEM
151282
Created by admin on Mon Mar 31 21:52:22 GMT 2025 , Edited by admin on Mon Mar 31 21:52:22 GMT 2025
PRIMARY
FDA UNII
0H4L5K3198
Created by admin on Mon Mar 31 21:52:22 GMT 2025 , Edited by admin on Mon Mar 31 21:52:22 GMT 2025
PRIMARY
CHEBI
74393
Created by admin on Mon Mar 31 21:52:22 GMT 2025 , Edited by admin on Mon Mar 31 21:52:22 GMT 2025
PRIMARY
NSC
88866
Created by admin on Mon Mar 31 21:52:22 GMT 2025 , Edited by admin on Mon Mar 31 21:52:22 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER