Record Information |
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Version | 1.0 |
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Creation date | 2015-10-09 22:32:40 UTC |
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Update date | 2017-01-19 02:36:36 UTC |
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FoodComEx ID | PC000789 |
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FoodDB Record | FDB022372 |
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Chemical Information |
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Name | N-Formyl-L-methionine |
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Description | Effective in the initiation of protein synthesis. The initiating methionine residue enters the ribosome as N-formylmethionyl tRNA. This process occurs in Escherichia coli and other bacteria as well as in the mitochondria of eucaryotic cells. [HMDB] |
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CAS Number | 4289-98-9 |
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Structure | |
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Synonyms | Synonym | Source |
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fMet | hmdb | For-Met-OH | hmdb | Formyl-L-methionine | hmdb | formylmethionine | hmdb | N-Formyl-L-methionine | hmdb | N-formyl-methionine | hmdb |
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Chemical Formula | C6H11NO3S |
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IUPAC name | (2R)-2-formamido-4-(methylsulfanyl)butanoic acid |
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InChI Identifier | InChI=1S/C6H11NO3S/c1-11-3-2-5(6(9)10)7-4-8/h4-5H,2-3H2,1H3,(H,7,8)(H,9,10)/t5-/m1/s1 |
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InChI Key | PYUSHNKNPOHWEZ-RXMQYKEDSA-N |
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Isomeric SMILES | CSCC[C@@H](NC=O)C(O)=O |
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Average Molecular Weight | 177.221 |
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Monoisotopic Molecular Weight | 177.045963913 |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as methionine and derivatives. Methionine and derivatives are compounds containing methionine or a derivative thereof resulting from reaction of methionine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. |
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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 | Methionine and derivatives |
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Alternative Parents | |
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Substituents | - Methionine or derivatives
- N-formyl-alpha-amino acid
- N-formyl-alpha amino acid or derivatives
- Thia fatty acid
- Fatty acyl
- Fatty acid
- Carboxamide group
- Secondary carboxylic acid amide
- Carboxylic acid
- Monocarboxylic acid or derivatives
- Thioether
- Sulfenyl compound
- Dialkylthioether
- Organosulfur compound
- Organooxygen compound
- Organonitrogen compound
- Organic oxygen compound
- Organic nitrogen compound
- Organopnictogen compound
- Hydrocarbon derivative
- Organic oxide
- 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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Physico-Chemical Properties - Experimental |
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Property | Value | Reference |
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Experimental logP | Not Available | |
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Experimental Water Solubility | Not Available | |
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Melting Point | Not Available | |
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Foods of Origin |
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Food | Content Range | Average | Reference |
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Food | | | Reference |
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Production Data |
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Production Method | commercial |
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Production Method Reference | Not Available |
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Production Method Reference File | Not Available |
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Quantity Available | Production upon request, up to 200 mg |
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Delivery Time | Not Available |
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Storage Form | solid |
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Storage Conditions | -80°C |
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Stability | Not Available |
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Purity | Not Available |
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Spectra |
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Spectral Data Upon Request | Not Available |
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Provider Information |
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Commercial Vendors |
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AKSci | V5922 |
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MetaSci | HMDB0001015 |
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Sigma-Aldrich | HMDB0001015 |
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Toronto Research Chemicals | F700693 |
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