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Record Information |
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| Version |
1.0 |
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| Update Date |
1/22/2018 11:54:54 AM |
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Metabolite ID | PAMDB001562 |
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Identification |
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| Name: |
2-Aminomalonate semialdehyde |
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| Description: | 2-Aminomalonate semialdehyde is an organic compound that can be formed from a reaction between NADP+ and L-serine. (EcoCyc) |
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Structure |
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| Synonyms: | - (2S)-2-amino-3-oxopropanoate
- (2S)-2-amino-3-oxopropanoic acid
- (S)-2-amino-3-oxopropanoate
- (S)-2-amino-3-oxopropanoic acid
- 2-Amino-3-oxo-Propanoate
- 2-Amino-3-oxo-Propanoic acid
- 2-Amino-3-oxopropionate
- 2-Amino-3-oxopropionic acid
- 2-Aminomalonate semialdehyde
- 2-Aminomalonic acid semialdehyde
- 2-Ammoniomalonate semialdehyde
- 2-Ammoniomalonic acid semialdehyde
- 2-Formylglycine
- 3-Oxo-(9CI)-Alanine
- 3-Oxo-L-alanine
- 3-Oxoalanine
- A-Formylglycine
- Alpha-Formylglycine
- Amino-(8CI)Malonaldehydate
- Amino-(8CI)Malonaldehydic acid
- L-3-Oxoalanine
- L-a-Formylglycine
- L-alpha-Formylglycine
- L-Amino-malonate semialdehyde
- L-Amino-malonic acid semialdehyde
- L-Aminomalonaldehydate
- L-Aminomalonaldehydic acid
- L-Serine semialdehyde [misnomer]
- L-α-Formylglycine
- α-Formylglycine
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Chemical Formula: |
C3H5NO3 |
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| Average Molecular Weight: |
103.0767 |
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| Monoisotopic Molecular
Weight: |
103.026943031 |
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| InChI Key: |
XMTCKNXTTXDPJX-REOHCLBHSA-N |
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| InChI: | InChI=1S/C3H5NO3/c4-2(1-5)3(6)7/h1-2H,4H2,(H,6,7)/t2-/m0/s1 |
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| CAS
number: |
5735-66-0 |
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| IUPAC Name: | (2S)-2-amino-3-oxopropanoic acid |
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Traditional IUPAC Name: |
2-aminomalonate semialdehyde |
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| SMILES: | N[C@@H](C=O)C(O)=O |
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Chemical Taxonomy |
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Taxonomy Description | This compound belongs to the class of organic compounds known as d-alpha-amino acids. These are alpha amino acids which have the D-configuration of the alpha-carbon atom. |
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Kingdom |
Organic compounds |
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| Super Class | Organic acids and derivatives |
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Class |
Carboxylic acids and derivatives |
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| Sub Class | Amino acids, peptides, and analogues |
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Direct Parent |
D-alpha-amino acids |
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| Alternative Parents |
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| Substituents |
- D-alpha-amino acid
- 1,3-dicarbonyl compound
- Monocarboxylic acid or derivatives
- Carboxylic acid
- Hydrocarbon derivative
- Primary amine
- Organooxygen compound
- Organonitrogen compound
- Primary aliphatic amine
- Carbonyl group
- Amine
- Aldehyde
- Aliphatic acyclic compound
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| Molecular Framework |
Aliphatic acyclic compounds |
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| External Descriptors |
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Physical Properties |
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| State: |
Solid |
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| Charge: | 0 |
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Melting point: |
Not Available |
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| Experimental Properties: |
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| Predicted Properties |
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Biological Properties |
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| Cellular Locations: |
Cytoplasm |
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| Reactions: | |
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Pathways: |
Not Available |
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Spectra |
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| Spectra: |
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References |
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| References: |
Not Available |
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| Synthesis Reference: |
Not Available |
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| Material Safety Data Sheet (MSDS) |
Not Available |
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Links |
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| External Links: |
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