Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C5H12N2OS |
| Molecular Weight | 148.227 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CSCC[C@H](N)C(N)=O
InChI
InChIKey=GSYTVXOARWSQSV-BYPYZUCNSA-N
InChI=1S/C5H12N2OS/c1-9-3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H2,7,8)/t4-/m0/s1
| Molecular Formula | C5H12N2OS |
| Molecular Weight | 148.227 |
| 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 |
|---|---|---|
| Aliphatic peptidyl hydroperoxides as a source of secondary oxidation in hydroxyl radical protein footprinting. | 2009-06 |
|
| Role of the [2Fe-2S]2+ cluster in biotin synthase: mutagenesis of the atypical metal ligand arginine 260. | 2006-11-28 |
|
| L: -Stereoselective amino acid amidase with broad substrate specificity from Brevundimonas diminuta: characterization of a new member of the leucine aminopeptidase family. | 2006-04 |
|
| Peptide models XLV: conformational properties of N-formyl-L-methioninamide and its relevance to methionine in proteins. | 2005-02-15 |
|
| Purification and properties of an enantioselective and thermoactive amidase from the thermophilic actinomycete Pseudonocardia thermophila. | 2004-07 |
|
| S-stereoselective piperazine-2-tert-butylcarboxamide hydrolase from Pseudomonas azotoformans IAM 1603 is a novel L-amino acid amidase. | 2004-04 |
|
| Kinetic studies of rat kidney gamma-glutamyltranspeptidase deacylation reveal a general base-catalyzed mechanism. | 2003-10-07 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:30:48 GMT 2025
by
admin
on
Mon Mar 31 21:30:48 GMT 2025
|
| Record UNII |
QSM06A70MD
|
| Record Status |
Validated (UNII)
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| Record Version |
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4510-08-1
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21362
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QSM06A70MD
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146480
Created by
admin on Mon Mar 31 21:30:48 GMT 2025 , Edited by admin on Mon Mar 31 21:30:48 GMT 2025
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