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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 | PAMDB004121 |
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Identification |
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| Name: |
(S)-Succinyldihydrolipoamide |
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| Description: | (S)-Succinyldihydrolipoamide is a metabolite (a product as well as a substrate) in glutamate degradation. It is also invovled in citrate cycle and is a reactant for oxoglutarate dehydrogenase (EC 1.2.4.2) and dihydrolipoyllysine-residue succinyltransferase (EC 2.3.1.61). |
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Structure |
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| Synonyms: | - 4-[(3R)-8-amino-8-oxo-1-Sulfanyloctan-3-yl]sulfanyl-4-oxobutanoate
- 4-[(3R)-8-amino-8-oxo-1-sulfanyloctan-3-yl]sulfanyl-4-oxobutanoic acid
- 4-[(3R)-8-amino-8-oxo-1-Sulphanyloctan-3-yl]sulphanyl-4-oxobutanoate
- 4-[(3R)-8-amino-8-oxo-1-Sulphanyloctan-3-yl]sulphanyl-4-oxobutanoic acid
- S-succinyl-dihydrolipoamide
- S-Succinyldihydrolipoamide
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Chemical Formula: |
C12H21NO4S2 |
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| Average Molecular Weight: |
307.429 |
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| Monoisotopic Molecular
Weight: |
307.091199545 |
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| InChI Key: |
RJCJWONCSKSHES-SECBINFHSA-N |
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| InChI: | InChI=1S/C12H21NO4S2/c13-10(14)4-2-1-3-9(7-8-18)19-12(17)6-5-11(15)16/h9,18H,1-8H2,(H2,13,14)(H,15,16)/t9-/m1/s1 |
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| CAS
number: |
Not Available |
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| IUPAC Name: | 4-{[(3R)-7-carbamoyl-1-sulfanylheptan-3-yl]sulfanyl}-4-oxobutanoic acid |
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Traditional IUPAC Name: |
4-{[(3R)-7-carbamoyl-1-sulfanylheptan-3-yl]sulfanyl}-4-oxobutanoic acid |
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| SMILES: | NC(=O)CCCC[C@H](CCS)SC(=O)CCC(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 thia fatty acids. These are fatty acid derivatives obtained by insertion of a sulfur atom at specific positions in the chain. |
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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 |
Thia fatty acids |
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| Alternative Parents |
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| Substituents |
- Fatty acyl thioester
- Thia fatty acid
- Fatty amide
- Thiocarboxylic acid ester
- Primary carboxylic acid amide
- Carboxamide group
- Sulfenyl compound
- Thioether
- Thiocarboxylic acid or derivatives
- Monocarboxylic acid or derivatives
- Carboxylic acid
- Carboxylic acid derivative
- Carboxylic acid amide
- Alkylthiol
- Hydrocarbon derivative
- Organosulfur compound
- Organooxygen compound
- Organonitrogen compound
- Carbonyl group
- 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: | -1 |
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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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Pathways: |
Not Available |
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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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