Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H5NO3 |
| Molecular Weight | 103.0767 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)CC(O)=O
InChI
InChIKey=CGJMROBVSBIBKP-UHFFFAOYSA-N
InChI=1S/C3H5NO3/c4-2(5)1-3(6)7/h1H2,(H2,4,5)(H,6,7)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Crystallization and preliminary X-ray crystallographic analysis of malonamidase E2, an amidase signature family member. | 2002 Mar |
|
| Identification of fonofos metabolites in Latuca sativa, Beta vulgaris, and Triticum aestivum by packed capillary flow fast atom bombardment tandem mass spectrometry. | 2002 Mar 27 |
|
| Practical synthesis of optically active alpha,alpha-disubstituted malonamic acids through asymmetric hydrolysis of malonamide derivatives with Rhodococcus sp. CGMCC 0497. | 2003 Mar 21 |
|
| Microbial transformation products of benzoxazolinone and benzoxazinone allelochemicals--a review. | 2004 Feb |
|
| Arg-158 is critical in both binding the substrate and stabilizing the transition-state oxyanion for the enzymatic reaction of malonamidase E2. | 2006 Dec 29 |
|
| The highly enantioselective phase-transfer catalytic mono-alkylation of malonamic esters. | 2009 Feb 21 |
|
| Substituted aryl malonamates as new serine beta-lactamase substrates: structure-activity studies. | 2010 Jan 1 |
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SUBSTANCE RECORD
