Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C5H11NO3 |
| Molecular Weight | 133.1457 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)[C@@H](N)[C@@H](C)O
InChI
InChIKey=TVHCXXXXQNWQLP-DMTCNVIQSA-N
InChI=1S/C5H11NO3/c1-3(7)4(6)5(8)9-2/h3-4,7H,6H2,1-2H3/t3-,4+/m1/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| NMR characterizations of the ice binding surface of an antifreeze protein. | 2010-12-28 |
|
| Architecture of y-family DNA polymerases relevant to translesion DNA synthesis as revealed in structural and molecular modeling studies. | 2010-09-16 |
|
| Generating a generation of proteasome inhibitors: from microbial fermentation to total synthesis of salinosporamide a (marizomib) and other salinosporamides. | 2010-03-25 |
|
| AtPIN: Arabidopsis thaliana protein interaction network. | 2009-12-31 |
|
| A versatile chemo-enzymatic route to enantiomerically pure beta-branched alpha-amino acids. | 2004-04-07 |
|
| Stereoselective addition of dimethyl thiophosphite to imines. | 2004-04-02 |
|
| Evaluation of the Escherichia coli threonine deaminase gene as a selectable marker for plant transformation. | 2004-03 |
|
| CD exciton chirality method for determination of the absolute configuration of beta-hydroxy-alpha-amino acid derivatives. | 2001-05-15 |
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222-158-1
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100000151979
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9FOK073U22
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DTXSID50955339
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3373-59-9
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2734894
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287508
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SUB126434
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SUBSTANCE RECORD