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
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
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
Title | Date | PubMed |
---|---|---|
Sites of hydroxyl radical reaction with amino acids identified by (2)H NMR detection of induced (1)H/(2)H exchange. | 2001 Feb 14 |
|
The membrane-associated lipoprotein-9 GmpC from Staphylococcus aureus binds the dipeptide GlyMet via side chain interactions. | 2004 Dec 28 |
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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 Nov |
|
Photo-CIDNP study of transient radicals of Met-Gly and Gly-Met peptides in aqueous solution at variable pH. | 2009 May 21 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:05:20 GMT 2023
by
admin
on
Sat Dec 16 08:05:20 GMT 2023
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Record UNII |
0H4L5K3198
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Record Status |
Validated (UNII)
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Record Version |
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Related Record | Type | Details | ||
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RACEMATE -> ENANTIOMER |