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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 | PAMDB110625 |
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Identification |
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| Name: |
O-acetyl-L-homoserine |
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| Description: | Zwitterionic form of O-acetyl-L-homoserine having an anionic carboxy group and a protonated α-amino group; major species at pH 7.3. |
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Structure |
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| Synonyms: | -
acetylhomoserine
-
O-acetylhomoserine
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Chemical Formula: |
C6H11NO4
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| Average Molecular Weight: |
161.16 |
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| Monoisotopic Molecular
Weight: |
162.0766328788 |
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| InChI Key: |
FCXZBWSIAGGPCB-YFKPBYRVSA-N |
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| InChI: |
InChI=1S/C6H11NO4/c1-4(8)11-3-2-5(7)6(9)10/h5H,2-3,7H2,1H3,(H,9,10)/t5-/m0/s1 |
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| CAS
number: |
Not Available |
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| IUPAC Name: | (2S)-4-acetoxy-2-azaniumylbutanoate |
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Traditional IUPAC Name: |
Not Available |
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| SMILES: | CC(OCCC(C([O-])=O)[N+])=O |
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Chemical Taxonomy |
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Taxonomy Description | This compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. |
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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 |
Alpha amino acids and derivatives |
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| Alternative Parents |
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| Substituents |
- Alpha-amino acid or derivatives
- Dicarboxylic acid or derivatives
- Fatty acid
- Carboxylic acid ester
- Carboxylic acid salt
- Carboxylic acid
- Organic nitrogen compound
- Organic salt
- Organic zwitterion
- Organooxygen compound
- Organonitrogen compound
- Hydrocarbon derivative
- Organic oxide
- Organopnictogen compound
- Organic oxygen 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: | 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: |
- L-methionine biosynthesis IIIHSERMETANA-PWY
- superpathway of sulfur amino acid biosynthesis (Saccharomyces cerevisiae)PWY-821
- L-homocysteine and L-cysteine interconversionPWY-801
- L-homocysteine biosynthesisPWY-5344
- sulfate assimilation 2PWY-781
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Spectra |
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| Spectra: |
Not Available |
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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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