Description
A monocarboxylic acid resulting from the formal 1,4-addition of one of the amino groups of urea to methacrylic acid (the Z isomer), or by the hydrolytic ring cleavage of uracil
Chemical properties
| Chemical formula | Net charge | Average mass |
|---|---|---|
| C5H8N2O3 | 0 | 144.130 |
-2-methylureidoacrylic acid.svg)
Nomenclature
| IUPAC | SMILES | InChI | InChIKey |
|---|---|---|---|
| (2Z)-3-(carbamoylamino)-2-methylacrylic acid | N(C(N)=O)/C=C(\C(O)=O)/C | InChI=1S/C5H8N2O3/c1-3(4(8)9)2-7-5(6)10/h2H,1H3,(H,8,9)(H3,6,7,10)/b3-2- | XHTOIFCGKIBYRK-IHWYPQMZSA-N |
Citations
- Adak, S, et al. 2017. RutA-Catalyzed Oxidative Cleavage of the Uracil Amide Involves Formation of a Flavin-N5-oxide. Biochemistry. 56(29).
- Mukherjee, T, et al. 2010. Catalysis of a flavoenzyme-mediated amide hydrolysis. Journal of the American Chemical Society. 132(16).