Record Information |
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Version |
1.0 |
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Update Date |
1/22/2018 12:54:54 PM |
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Metabolite ID | PAMDB120308 |
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Identification |
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Name: |
(2R,4S)-2-methyl-2,3,3,4-tetrahydroxytetrahydrofuran |
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Description: | A tetrahydroxytetrahydrofuran in which the hydroxy groups are located at positions 2, 3, 4, and 4 and which is substituted by a methyl group at position 2 (the 2R,4S diastereoisomer). |
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Structure |
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Synonyms: | - (2R,4S)-2-METHYL-2,3,3,4-TETRAHYDROXYTETRAHYDROFURAN
- (2R,4S)-2-methyldihydrofuran-2,3,3,4(2H)-tetrol
- (2R,4S)-2-methyloxolane-2,3,3,4-tetrol
- (2R,4S)-2-methyltetrahydrofuran-2,3,3,4-tetrol
- (R)-THMF
- AI-2
- auto inducer 2
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Chemical Formula: |
C5H10O5 |
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Average Molecular Weight: |
150.131 |
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Monoisotopic Molecular
Weight: |
150.05283 |
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InChI Key: |
BVIYGXUQVXBHQS-IUYQGCFVSA-N |
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InChI: | InChI=1S/C5H10O5/c1-4(7)5(8,9)3(6)2-10-4/h3,6-9H,2H2,1H3/t3-,4+/m0/s1 |
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CAS
number: |
Not Available |
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IUPAC Name: | (2R,4S)-2-methyltetrahydrofuran-2,3,3,4-tetrol |
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Traditional IUPAC Name: |
Not Available |
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SMILES: | CC1(O)(OCC(O)C(O)(O)1) |
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Chemical Taxonomy |
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Taxonomy Description | This compound belongs to the class of organic compounds known as pentoses. These are monosaccharides in which the carbohydrate moiety contains five carbon atoms. |
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Kingdom |
Organic compounds |
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Super Class | Organic oxygen compounds |
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Class |
Organooxygen compounds |
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Sub Class | Carbohydrates and carbohydrate conjugates |
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Direct Parent |
Pentoses |
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Alternative Parents |
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Substituents |
- Pentose monosaccharide
- Oxolane
- Secondary alcohol
- Hemiacetal
- Oxacycle
- Organoheterocyclic compound
- Polyol
- Carbonyl hydrate
- Hydrocarbon derivative
- Alcohol
- Aliphatic heteromonocyclic compound
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Molecular Framework |
Aliphatic heteromonocyclic compounds |
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External Descriptors |
- a small molecule (CPD-10776)
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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: |
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Spectra |
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Spectra: |
Not Available |
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References |
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References: |
- Miller ST, Xavier KB, Campagna SR, Taga ME, Semmelhack MF, Bassler BL, Hughson FM (2004)Salmonella typhimurium recognizes a chemically distinct form of the bacterial quorum-sensing signal AI-2. Molecular cell 15, Pubmed: 15350213
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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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