| Record Information |
|---|
| Version | 1.0 |
|---|
| Creation Date | 2016-09-30 22:45:43 UTC |
|---|
| Update Date | 2020-05-21 16:28:30 UTC |
|---|
| BMDB ID | BMDB0001422 |
|---|
| Secondary Accession Numbers | |
|---|
| Metabolite Identification |
|---|
| Common Name | 3-Hydroxy-N6,N6,N6-trimethyl-L-lysine |
|---|
| Description | 3-Hydroxy-N6,N6,N6-trimethyl-L-lysine belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom. 3-Hydroxy-N6,N6,N6-trimethyl-L-lysine is possibly soluble (in water) and a very strong basic compound (based on its pKa). 3-Hydroxy-N6,N6,N6-trimethyl-L-lysine exists in all living organisms, ranging from bacteria to humans. 3-Hydroxy-N6,N6,N6-trimethyl-L-lysine participates in a number of enzymatic reactions, within cattle. In particular, 3-Hydroxy-N6,N6,N6-trimethyl-L-lysine and succinic acid can be biosynthesized from N6,N6,N6-trimethyl-L-lysine and oxoglutaric acid through its interaction with the enzyme trimethyllysine dioxygenase, mitochondrial. In addition, 3-Hydroxy-N6,N6,N6-trimethyl-L-lysine can be converted into glycine and 4-trimethylammoniobutanal; which is mediated by the enzyme serine hydroxymethyltransferase, cytosolic. In cattle, 3-hydroxy-N6,N6,N6-trimethyl-L-lysine is involved in the metabolic pathway called carnitine synthesis pathway. |
|---|
| Structure | |
|---|
| Synonyms | | Value | Source |
|---|
| 3-Hydroxy-N(6),N(6),N(6)-trimethyl-L-lysine | HMDB | | 3-Hydroxy-N(6),N(6),N(6)-trimethyllysine | HMDB | | 3-Hydroxy-N6,N6,N6-trimethyl-L-lysin-N6-ium | HMDB |
|
|---|
| Chemical Formula | C9H21N2O3 |
|---|
| Average Molecular Weight | 205.2746 |
|---|
| Monoisotopic Molecular Weight | 205.155217548 |
|---|
| IUPAC Name | [(5S)-5-amino-5-carboxy-4-hydroxypentyl]trimethylazanium |
|---|
| Traditional Name | [(5S)-5-amino-5-carboxy-4-hydroxypentyl]trimethylazanium |
|---|
| CAS Registry Number | Not Available |
|---|
| SMILES | C[N+](C)(C)CCCC(O)[C@H](N)C(O)=O |
|---|
| InChI Identifier | InChI=1S/C9H20N2O3/c1-11(2,3)6-4-5-7(12)8(10)9(13)14/h7-8,12H,4-6,10H2,1-3H3/p+1/t7?,8-/m0/s1 |
|---|
| InChI Key | ZRJHLGYVUCPZNH-MQWKRIRWSA-O |
|---|
| Chemical Taxonomy |
|---|
| Description | belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom. |
|---|
| Kingdom | Organic compounds |
|---|
| Super Class | Organic acids and derivatives |
|---|
| Class | Carboxylic acids and derivatives |
|---|
| Sub Class | Amino acids, peptides, and analogues |
|---|
| Direct Parent | L-alpha-amino acids |
|---|
| Alternative Parents | |
|---|
| Substituents | - L-alpha-amino acid
- Medium-chain hydroxy acid
- Medium-chain fatty acid
- Amino fatty acid
- Beta-hydroxy acid
- Hydroxy fatty acid
- Hydroxy acid
- Fatty acid
- Fatty acyl
- Tetraalkylammonium salt
- Quaternary ammonium salt
- Amino acid
- Secondary alcohol
- Carboxylic acid
- Monocarboxylic acid or derivatives
- Hydrocarbon derivative
- Amine
- Primary amine
- Organooxygen compound
- Organonitrogen compound
- Primary aliphatic amine
- Organic oxide
- Organopnictogen compound
- Alcohol
- Organic salt
- Carbonyl group
- Organic oxygen compound
- Organic nitrogen compound
- Organic cation
- Aliphatic acyclic compound
|
|---|
| Molecular Framework | Aliphatic acyclic compounds |
|---|
| External Descriptors | |
|---|
| Ontology |
|---|
| Status | Expected but not Quantified |
|---|
| Origin | |
|---|
| Biofunction | Not Available |
|---|
| Application | Not Available |
|---|
| Cellular locations | |
|---|
| Physical Properties |
|---|
| State | Solid |
|---|
| Experimental Properties | | Property | Value | Reference |
|---|
| Melting Point | Not Available | Not Available | | Boiling Point | Not Available | Not Available | | Water Solubility | Not Available | Not Available | | LogP | Not Available | Not Available |
|
|---|
| Predicted Properties | |
|---|
| Spectra |
|---|
| Spectra | |
|---|
