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Record Information |
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| Version |
1.0 |
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| Update Date |
1/22/2018 12:54:54 PM |
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Metabolite ID | PAMDB120185 |
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Identification |
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| Name: |
N-formyl-L-glutamate |
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| Description: | A doubly-charged N-acyl-L-α-amino acid anion resulting from deprotonation of both carboxy groups of N-formyl-L-glutamic acid. |
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Structure |
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| Synonyms: | - (2S)-2-(formylamino)pentanedioate
- N-formyl-L-glutamate
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Chemical Formula: |
C6H7NO5 |
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| Average Molecular Weight: |
173.125 |
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| Monoisotopic Molecular
Weight: |
175.04807 |
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| InChI Key: |
ADZLWSMFHHHOBV-BYPYZUCNSA-L |
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| InChI: | InChI=1S/C6H9NO5/c8-3-7-4(6(11)12)1-2-5(9)10/h3-4H,1-2H2,(H,7,8)(H,9,10)(H,11,12)/p-2/t4-/m0/s1 |
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| CAS
number: |
1681-96-5 |
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| IUPAC Name: | (2S)-2-formamidopentanedioate |
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Traditional IUPAC Name: |
N-formyl-L-glutamic acid |
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| SMILES: | C(=O)NC(CCC(=O)[O-])C(=O)[O-] |
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Chemical Taxonomy |
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Taxonomy Description | This compound belongs to the class of chemical entities known as glutamic acid and derivatives. These are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. |
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Kingdom |
Chemical entities |
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| Super Class | Organic compounds |
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Class |
Organic acids and derivatives |
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| Sub Class | Carboxylic acids and derivatives |
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Direct Parent |
Glutamic acid and derivatives |
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| Alternative Parents |
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| Substituents |
- Glutamic acid or derivatives
- N-acyl-l-alpha-amino acid
- N-formyl-alpha-amino acid
- N-formyl-alpha amino acid or derivatives
- Dicarboxylic acid or derivatives
- Fatty acid
- Secondary carboxylic acid amide
- Carboxamide group
- Carboxylic acid
- Organopnictogen compound
- Carbonyl group
- Organooxygen compound
- Organonitrogen compound
- Organic oxygen compound
- Organic nitrogen compound
- Hydrocarbon derivative
- Organic oxide
- 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: | -2 |
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Melting point: |
Not Available |
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| Experimental Properties: |
| Property | Value | Reference |
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| Melting Point | Not Available | Not Available | | Boiling Point | Not Available | Not Available | | Water Solubility | Not Available | Not Available | | LogP | Not Available | Not Available |
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| Predicted Properties |
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Biological Properties |
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| Cellular Locations: |
Not Available |
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| Reactions: | |
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Pathways: |
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Spectra |
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| Spectra: |
Not Available |
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References |
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| References: |
- Martí-Arbona R, Xu C, Steele S, Weeks A, Kuty GF, Seibert CM, Raushel FM (2006)Annotating enzymes of unknown function: N-formimino-L-glutamate deiminase is a member of the amidohydrolase superfamily. Biochemistry 45, Pubmed: 16475788
- Coote JG, Hassall H (1973)The degradation of L-histidine, imidazolyl-L-lactate and imidazolylpropionate by Pseudomonas testosteroni. The Biochemical journal 132, Pubmed: 4146796
- Haas D, Leisinger T (1975)N-acetylglutamate 5-phosphotransferase of Pseudomonas aeruginosa. Catalytic and regulatory properties. European journal of biochemistry 52, Pubmed: 240684
- Hu L, Mulfinger LM, Phillips AT (1987)Purification and properties of formylglutamate amidohydrolase from Pseudomonas putida. Journal of bacteriology 169, Pubmed: 3308850
- Miyake M, Innami T, Kakimoto Y (1983)A beta-citryl-L-glutamate-hydrolysing enzyme in rat testes. Biochimica et biophysica acta 760, Pubmed: 6414521
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| Synthesis Reference: |
Borek, Blanche Ann; Waelsch, Heinrich. The enzymic degradation of histidine. Journal of Biological Chemistry (1953), 205 459-74. |
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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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