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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 | PAMDB100020 |
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Identification |
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| Name: |
N-isopropyl-L-glutamine |
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| Description: | A N5-alkylglutamine where the alkyl group is isopropyl. |
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Structure |
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| Synonyms: | - γ-glutamyl-isopropylamide
- N5-isopropyl-L-glutamine
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Chemical Formula: |
C8H16N2O3 |
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| Average Molecular Weight: |
188.2242 |
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| Monoisotopic Molecular
Weight: |
188.116 |
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| InChI Key: |
CABXGBMKSVRWOG-LURJTMIESA-N |
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| InChI: | InChI=1S/C8H16N2O3/c1-5(2)10-7(11)4-3-6(9)8(12)13/h5-6H,3-4,9H2,1-2H3,(H,10,11)(H,12,13)/t6-/m0/s1 |
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| CAS
number: |
Not Available |
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| IUPAC Name: | N-propan-2-yl-L-glutamine |
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Traditional IUPAC Name: |
Not Available |
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| SMILES: | CC(C)NC(=O)CC[C@H](N)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 glutamine and derivatives. These are compounds containing glutamine or a derivative thereof resulting from reaction of glutamine 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 |
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 |
Glutamine and derivatives |
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| Alternative Parents |
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| Substituents |
- Glutamine or derivatives
- Alpha-amino acid
- L-alpha-amino acid
- Fatty amide
- N-acyl-amine
- Fatty acyl
- Fatty acid
- Carboxamide group
- Carboxylic acid salt
- Amino acid
- Secondary carboxylic acid amide
- Carboxylic acid
- Monocarboxylic acid or derivatives
- Primary amine
- Organooxygen compound
- Organonitrogen compound
- Hydrocarbon derivative
- Organic nitrogen compound
- Primary aliphatic amine
- Organic oxide
- Organopnictogen compound
- Organic oxygen compound
- Carbonyl group
- Amine
- Organic salt
- Organic zwitterion
- Aliphatic acyclic compound
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| Molecular Framework |
Aliphatic acyclic compounds |
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| External Descriptors |
- N(5)-alkyl-L-glutamine (CHEBI:85891)
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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: |
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: |
- de Azevedo Wäsch SI, van der Ploeg JR, Maire T, Lebreton A, Kiener A,
Leisinger T. Transformation of isopropylamine to L-alaninol by Pseudomonas sp.
strain KIE171 involves N-glutamylated intermediates. Appl Environ Microbiol. 2002
May;68(5):2368-75. Pubmed: 11976110
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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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