L-xylulose
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L-xylulose Eigenschaften
- Schmelzpunkt:
- Not Applicable
- Siedepunkt:
- 469.1±45.0 °C(Predicted)
- Dichte
- 1.516±0.06 g/cm3(Predicted)
- Flammpunkt:
- >230 °F
- storage temp.
- 2-8°C
- L?slichkeit
- Methanol (Slightly), Water (Soluble)
- Aggregatzustand
- syrup
- pka
- 11.90±0.20(Predicted)
- Farbe
- light yellow
- Optische Aktivit?t
- +33
- LogP
- -1.200 (est)
Sicherheit
WGK Germany | 3 | ||
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HS Code | 29400090 |
L-xylulose Chemische Eigenschaften,Einsatz,Produktion Methoden
Chemische Eigenschaften
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).Verwenden
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).synthetische
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 Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
L-xylulose Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.
Global( 54)Lieferanten
Firmenname | Telefon | Land | Produktkatalog | Edge Rate | |
---|---|---|---|---|---|
BOC Sciences | +1-631-485-4226 |
inquiry@bocsci.com | United States | 19553 | 58 |
Shaanxi Dideu Medichem Co. Ltd | +86-29-87569266 15319487004 |
1015@dideu.com | China | 3939 | 58 |
Career Henan Chemica Co | +86-0371-86658258 +8613203830695 |
laboratory@coreychem.com | China | 30233 | 58 |
Wuhan Fortuna Chemical Co., Ltd | +86-027-59207850 |
info@fortunachem.com | China | 5971 | 58 |
Watson Biotechnology Co.,Ltd | +86-18186686046 +86-18186686046 |
sales01@watsonbiotech.cn | China | 5859 | 58 |
TargetMol Chemicals Inc. | +8613564774135 |
zijue.cai@tsbiochem.com | United States | 19881 | 58 |
Amadis Chemical Company Limited | 571-89925085 |
sales@amadischem.com | China | 131957 | 58 |
J & K SCIENTIFIC LTD. | 010-82848833 400-666-7788 |
jkinfo@jkchemical.com | China | 96815 | 76 |
Hunan Hui Bai Shi Biotechnology Co., Ltd. | 0731-85526065 13308475853 |
ivy@hnhbsj.com | China | 4555 | 62 |
BOC Sciences | 1-631-485-4226; 16314854226 |
info@bocsci.com | United States | 14055 | 65 |
527-50-4()Verwandte Suche:
β,ε-Carotin-3,3'-diol
(R)-5-(1,5-Dimethyl-4-hexenyl)-o-kresol
Saccharose
Sucroseoctaacetat
Melizitose
D-Fructose, 1,6-Bis(dihydrogen-phosphat), Trinatriumsalz
O-β-D-glucopyranosyl-(1-6)-β-D-fructofuranosyl-α-D-glucopyranosid
Fructose-1-(bariumphosphat)
Octakis(O-2-hydroxypropyl)sucrose
Stachyose
Octakis-O-(2-cyanethyl)sucrose
Sucrosepalmitat
Sucrosedi(acetat)hexaisobutyrat
O-2,3,4,6-Tetra-O-acetyl-α-D-galaktopyranosyl-(1-6)-1,3,4-tri-O-acetyl-β-D-fructofuranosyl-α-D-glucopyranosidtetraacetat
- 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
- L-Threo-2-pentulose
- L-Xylulose - 1.0 M aqueous solution
- L-Xylulose (1.0 M in water)
- laevo-xylulose
- (3R,4S)-1,3,4,5-Tetrahydroxypentan-2-one
- Xanthone Impurity 18
- 527-50-4
- BioChemical
- Carbohydrate
- Metabolites and Cofactors on the Metabolic Pathways Chart
- Metabolic Pathways
- Metabolomics
- CARBOHYDRATE