- L-xylulose
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- $0.00 / 10G
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2023-02-16
- CAS:527-50-4
- Min. Order: 10G
- Purity: 98%min
- Supply Ability: 30kg/month
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| L-xylulose Basic information |
Product Name: | L-xylulose | Synonyms: | L-XYLULOSE;L-THREO-PENTULOSE;threo-2-Pentulose, L-threo-Pentulose;L-Xylulose ,98%;L-Xylulose - Aqueous solution;L-threo-2-Pentulose (9CI);threo-2-pentulose;(3R,4S)-2-(hydroxymethyl)oxolane-2,3,4-triol | CAS: | 527-50-4 | MF: | C5H10O5 | MW: | 150.13 | EINECS: | | Product Categories: | CARBOHYDRATE | Mol File: | 527-50-4.mol | |
| L-xylulose Chemical Properties |
Melting point | Not Applicable | Boiling point | 469.1±45.0 °C(Predicted) | density | 1.516±0.06 g/cm3(Predicted) | Fp | >230 °F | storage temp. | 2-8°C | solubility | Methanol (Slightly), Water (Soluble) | form | syrup | pka | 11.90±0.20(Predicted) | color | light yellow | LogP | -1.200 (est) |
WGK Germany | 3 | HS Code | 29400090 |
| L-xylulose Usage And Synthesis |
Chemical Properties | L-xylulose is a clear liquid. It is a ketopentose, meaning that it has five carbon atoms and a ketogroup at carbon C-2. It has a molecular formula of C5H10O5 and a molar mass of 150.13 g/mol. Xylulose is almost colorless and it forms syrup. The formation of crystals has not been reported (Budavari, 1996). Both D- and L - enantiomers of xylulose are found as intermediates in metabolic pathways of prokaryotes as well as eukaryotes. Both forms are rare in nature (Doten and Mortlock, 1985b). | Uses | L-Xylulose is used in studies relating to potential inhibitors of glycosidases and has been proven to inhibit oligosaccharide processing to a degree. | Definition | ChEBI: L-xylulose is a xylulose. It has a role as a human metabolite, an Escherichia coli metabolite and a mouse metabolite. It is an enantiomer of a D-xylulose. | Application | L-Xylulose has been shown to be a specific inhibitor of certain α-glucosidases,while having virtually no effect on other glycosidases such as β-glucosidase or α- and β-mannosidases. Furthermore,it is a specific inhibitor of the N-linked glycoproteinprocessing enzyme,glucosidase I, but does not inhibit glucosidase I or otherglycoprotein processing mannosidases. Thus it could prove to be a useful inhibitor forstudying glycoprotein processing, especially as it has been proven to be non-toxic andto also be effective in cell cultures (Muniruzzaman et al., 1996). L-Xylulose has been shown to have a strong inhibitory effect on the a-glucosidases,sucrase and maltase, present in the small intestine. Thus, an L-xylulose containing drug preparation for reducing blood sugar levels in humans and animals has been patented (Heinz et al.,1998). | Preparation | In 1933 a synthetic procedure for producing small amounts of D- and L -xylulose was introduced. In this method D- or L-xylose is epimerized to the corresponding diastereomer. The isomerization of xylose in pyridine leads to the production of xylulose (Touster, 1962). This enzyme catalyzes the production of L-xylulose from xylitol using either PQQ (pyrroloquinoline quinone) or FAD (flavin adenine dinucleotide) as prosthetic group, and L-xylulose is accumulated in the medium (Adachi et al., 1999; Adachi et al., 2001). |
| L-xylulose Preparation Products And Raw materials |
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