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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 | PAMDB110127 |
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Identification |
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| Name: |
N-succinyl-2-amino-6-ketopimelate |
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| Description: | N-Succinyl-2-amino-6-ketopimelate is an intermediate in lysine biosynthesis. It is the fourth to last step in the synthesis of lysine and is converted. from tetrahydrodipicolinate via the enzyme tetrahydrodipicolinate N-succinyltransferase (EC 2.3.1.117). It is then converted to N-succinyl-L,L-2,6-diaminopimelate via the enzyme Succinyldiaminopimelate transferase (EC 2.6.1.17). |
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Structure |
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| Synonyms: | -
N-Succinyl-2-L-amino-6-oxoheptanedioate
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N-succinyl-L-2-amino-6-oxoheptanedioate
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succinyl-ε-keto-α-aminopimelate
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Chemical Formula: |
C11H12NO8
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| Average Molecular Weight: |
286.22 |
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| Monoisotopic Molecular
Weight: |
289.0797664635 |
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| InChI Key: |
SDVXSCSNVVZWDD-LURJTMIESA-K |
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| InChI: |
InChI=1S/C11H15NO8/c13-7(11(19)20)3-1-2-6(10(17)18)12-8(14)4-5-9(15)16/h6H,1-5H2,(H,12,14)(H,15,16)(H,17,18)(H,19,20)/p-3/t6-/m0/s1 |
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| CAS
number: |
Not Available |
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| IUPAC Name: | (2S)-2-(3-carboxylatopropanamido)-6-oxoheptanedioate |
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Traditional IUPAC Name: |
(2S)-2-(3-carboxypropanamido)-6-oxoheptanedioic acid |
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| SMILES: | C(CC(=O)C(=O)[O-])CC(NC(CCC([O-])=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 n-acyl-l-alpha-amino acids. These are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom. |
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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 |
N-acyl-L-alpha-amino acids |
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| Alternative Parents |
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| Substituents |
- N-acyl-l-alpha-amino acid
- Tricarboxylic acid or derivatives
- Alpha-keto acid
- Fatty amide
- Keto acid
- Fatty acyl
- N-acyl-amine
- Alpha-hydroxy ketone
- Carboxamide group
- Secondary carboxylic acid amide
- Ketone
- Carboxylic acid
- Organooxygen compound
- Hydrocarbon derivative
- Organic oxide
- Organopnictogen compound
- Carbonyl group
- Organic oxygen compound
- Organic nitrogen compound
- Organonitrogen compound
- 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: | -3 |
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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: |
- superpathway of L-lysine, L-threonine and L-methionine biosynthesis IP4-PWY
- L-lysine biosynthesis IDAPLYSINESYN-PWY
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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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