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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 | PAMDB100012 |
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Identification |
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| Name: |
iminoarginine |
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| Description: | A dehydroamino acid that is arginine in which the amino group has been oxidised to the corresponding imine. |
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Structure |
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| Synonyms: | Not Available |
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Chemical Formula: |
C6H12N4O2 |
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| Average Molecular Weight: |
172.1851 |
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| Monoisotopic Molecular
Weight: |
172.096 |
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| InChI Key: |
YWGYOCPWFDUKSA-UHFFFAOYSA-N |
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| InChI: | InChI=1S/C6H12N4O2/c7-4(5(11)12)2-1-3-10-6(8)9/h7H,1-3H2,(H,11,12)(H4,8,9,10) |
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| CAS
number: |
Not Available |
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| IUPAC Name: | 5-carbamimidamido-2-iminopentanoic acid |
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Traditional IUPAC Name: |
Not Available |
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| SMILES: | NC(=N)NCCCC(=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 fatty acids and conjugates. These are aliphatic monocarboxylic acids with a saturated or unsaturated aliphatic tail (with at least 4 Carbon atoms). |
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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 acids and conjugates |
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Direct Parent |
Fatty acids and conjugates |
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| Alternative Parents |
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| Substituents |
- Fatty acid
- Guanidine
- Ketimine
- Organic 1,3-dipolar compound
- Propargyl-type 1,3-dipolar organic compound
- Carboximidamide
- Monocarboxylic acid or derivatives
- Carboxylic acid
- Carboxylic acid derivative
- Organic oxide
- Hydrocarbon derivative
- Organic nitrogen compound
- Organooxygen compound
- Organonitrogen compound
- Carbonyl group
- Imine
- Organopnictogen compound
- Organic oxygen compound
- Aliphatic acyclic compound
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| Molecular Framework |
Aliphatic acyclic compounds |
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| External Descriptors |
- guanidines, dehydroamino acid, ketimine, arginine derivative (CHEBI:84259)
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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: |
- Gannavaram S, Sirin S, Sherman W, Gadda G. Mechanistic and computational
studies of the reductive half-reaction of tyrosine to phenylalanine active site
variants of D-arginine dehydrogenase. Biochemistry. 2014 Oct 21;53(41):6574-83.
Pubmed: 25243743
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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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