| Record Information |
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| Version | 2.0 |
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| Creation Date | 2012-10-10 12:15:18 -0600 |
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| Update Date | 2015-06-03 17:25:53 -0600 |
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| Secondary Accession Numbers | |
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| Identification |
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| Name: | Iminobutyrate |
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| Description | Iminobutyrate is a short-lived, unstable intermediate that appears in the degradation or dehydration of threonine via L-threonine dehydratase. It is a tautomer of aminocrotonate, which tautomerizes to its imine form iminobutyrate. |
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| Structure | |
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| Synonyms: | |
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| Chemical Formula: | C6H11NO2 |
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| Weight: | Average: 129.157
Monoisotopic: 129.078978601 |
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| InChI Key: | YPMPTULBFPFSEQ-UHFFFAOYSA-N |
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| InChI: | InChI=1S/C6H11NO2/c1-3-9-6(8)4-5(2)7/h4H,3,7H2,1-2H3 |
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| CAS number: | Not Available |
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| IUPAC Name: | ethyl 3-aminobut-2-enoate |
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| Traditional IUPAC Name: | ethyl 3-aminobut-2-enoate |
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| SMILES: | CCOC(=O)C=C(C)N |
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| Chemical Taxonomy |
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| Description | belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. |
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| Kingdom | Organic compounds |
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| Super Class | Lipids and lipid-like molecules |
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| Class | Fatty Acyls |
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| Sub Class | Fatty acid esters |
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| Direct Parent | Fatty acid esters |
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| Alternative Parents | |
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| Substituents | - Fatty acid ester
- Enoate ester
- Alpha,beta-unsaturated carboxylic ester
- Vinylogous amide
- Amino acid or derivatives
- Carboxylic acid ester
- Monocarboxylic acid or derivatives
- Enamine
- Carboxylic acid derivative
- Organopnictogen compound
- Organic oxygen compound
- Primary amine
- Organooxygen compound
- Organonitrogen compound
- Primary aliphatic amine
- Organic nitrogen compound
- Amine
- Carbonyl group
- Organic oxide
- Hydrocarbon derivative
- Aliphatic acyclic compound
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| Molecular Framework | Aliphatic acyclic compounds |
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| External Descriptors | Not Available |
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| Physical Properties |
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| State: | Not Available |
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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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| SMPDB Pathways: | Not Available |
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| KEGG Pathways: | Not Available |
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| EcoCyc Pathways: | Not Available |
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| Concentrations |
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| Not Available |
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| Spectra |
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| Spectra: | |
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| References |
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| References: | - Yurtsever D. (2007). Fatty acid methyl ester profiling of Enterococcus and Esherichia coli for microbial source tracking. M.sc. Thesis. Villanova University: U.S.A
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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: | | Resource | Link |
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| CHEBI ID | Not Available | | HMDB ID | Not Available | | Pubchem Compound ID | 95308 | | Kegg ID | Not Available | | ChemSpider ID | Not Available | | Wikipedia ID | Not Available | | BioCyc ID | Not Available |
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