Rhamnose
Names | |
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IUPAC name
(2R,3R,4R,5R,6S)-6-Methyloxane-2,3,4,5-tetrol
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Other names
Isodulcit
α-L-Rhamnose L-Rhamnose L-Mannomethylose α-L-Rha α-L-Rhamnoside α-L-Mannomethylose 6-Deoxy-L-mannose Rhamnopyranose Rhamnopyranoside |
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Identifiers | |
10485-94-6 | |
ChEBI | CHEBI:16055 |
ChemSpider | 18150 |
DrugBank | DB01869 |
Jmol 3D model | Interactive image |
KEGG | C00507 |
PubChem | 19233 |
UNII | QN34XC755A |
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Properties | |
C6H12O5 | |
Molar mass | 164.16 g·mol−1 |
Density | 1.41 g/mL |
Melting point | 91 to 93 °C (196 to 199 °F; 364 to 366 K) (monohydrate) |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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verify (what is ?) | |
Infobox references | |
Rhamnose (Rham) is a naturally occurring deoxy sugar. It can be classified as either a methyl-pentose or a 6-deoxy-hexose. Rhamnose occurs in nature in its L-form as L-rhamnose (6-deoxy-L-mannose). This is unusual, since most of the naturally occurring sugars are in D-form. Exceptions are the methyl pentoses L-fucose and L-rhamnose and the pentose L-arabinose.
Rhamnose can be isolated from Buckthorn (Rhamnus), poison sumac, and plants in the genus Uncaria. Rhamnose is also produced by microalgae belonging to the Bacillariophyceae.[2]
Rhamnose is commonly bound to other sugars in nature. It is a common glycone component of glycosides from many plants. Rhamnose is also a component of the outer cell membrane of acid-fast bacteria in the Mycobacterium genus, which includes the organism that causes tuberculosis.[3]
References
- ↑ Merck Index, 11th Edition, 8171.
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External links
- Use of L-rhamnose to Study Irreversible Adsorption of Bacteriophage PL-1 to a Strain of Lactobacillus casei Journal of General Virology