Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C4H8N2O3 |
| Molecular Weight | 132.1179 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
N[C@H](CC(N)=O)C(O)=O
InChI
InChIKey=DCXYFEDJOCDNAF-UWTATZPHSA-N
InChI=1S/C4H8N2O3/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H2,6,7)(H,8,9)/t2-/m1/s1
PubMed
| Title | Date | PubMed |
|---|---|---|
| The discovery of stereoselectivity at biological receptors: Arnaldo Piutti and the taste of the asparagine enantiomers--history and analysis on the 125th anniversary. | 2012-12 |
|
| Modified ammonia electrode method to investigate D-asparagine breakdown by Campylobacter strains. | 1986-04 |
|
| Utilization of D-asparagine by Saccharomyces cerevisiae. | 1976-03 |
|
| Inhibition of L-asparaginase in extracts of Mycobacterium phlei by D-asparagine. | 1956-03-31 |
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2058-58-4
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50349
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m2097
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74337
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DTXSID30872479
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218-163-3
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T6QV1010K6
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28159
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439600
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DB03943
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SUBSTANCE RECORD
