α-D-Lyxopyranose
α-D-Lyxopyranose structure
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Common Name | α-D-Lyxopyranose | ||
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| CAS Number | 1114-34-7 | Molecular Weight | 150.130 | |
| Density | 1.8±0.1 g/cm3 | Boiling Point | 333.2±42.0 °C at 760 mmHg | |
| Molecular Formula | C5H10O5 | Melting Point | 108-112ºC(lit.) | |
| MSDS | Chinese USA | Flash Point | 155.3±27.9 °C | |
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Chiral separation of D/L-aldoses by micellar electrokinetic chromatography using a chiral derivatization reagent and a phenylboronic acid complex.
Anal. Bioanal. Chem 407 , 6201-6, (2015) A novel method was developed for D/L-isomeric separation of aldopentoses and aldohexoses as their (S)-(+)-4-(N,N-dimethylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole derivatives using phenylboronate buffer containing sodium dodecyl sulfate a... |
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Involvement of TRPV1 and AQP2 in hypertonic stress by xylitol in odontoblast cells.
Connect. Tissue Res. 56(1) , 44-9, (2015) To examine the responses of mouse odontoblast-lineage cell line (OLC) cultures to xylitol-induced hypertonic stress.OLCs were treated with xylitol, sucrose, sorbitol, mannitol, arabinose and lyxose. Cell viability was evaluated using the 3-(4,5-dimethylthiazo... |
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HPLC separation of all aldopentoses and aldohexoses on an anion-exchange stationary phase prepared from polystyrene-based copolymer and diamine: the effect of NaOH eluent concentration.
Molecules 16(7) , 5905-15, (2011) To investigate the separations of all aldopentoses (ribose, arabinose, xylose and lyxose) and aldohexoses (glucose, galactose, allose, altrose, mannose, gulose, idose and talose) on the D₆ stationary phase prepared by the reaction of chloromethylated styrene-... |
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Asymmetric histidine-catalyzed cross-aldol reactions of enolizable aldehydes: access to defined configured quaternary stereogenic centers.
J. Am. Chem. Soc. 131(46) , 16642-3, (2009) A histidine-catalyzed asymmetric direct cross-aldol reaction of enolizable aldehydes is described. In contrast to proline, histidine is able to clearly differentiate the reactivity of various aldehydes. In addition, this approach provides access to syn-config... |
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Characterization of a recombinant thermostable D-lyxose isomerase from Dictyoglomus turgidum that produces D-lyxose from D-xylulose.
Biotechnol. Lett. 34(6) , 1079-85, (2012) A putative D-lyxose isomerase from Dictyoglomus turgidum was purified with a specific activity of 19 U/mg for D-lyxose isomerization by heat treatment and affinity chromatography. The native enzyme was estimated as a 42 kDa dimer by gel-filtration chromatogra... |
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Dibutylsilylene-pentose bis-chelates: on the glycoses' binding sites for strongly Lewis-acidic centres.
Carbohydr. Res. 346(13) , 1767-75, (2011) Excess di(tert-butyl)silylene (DTBS) bis(trifluoromethanesulfonate) formed bis-DTBS derivatives with the four aldopentoses (arabinose, lyxose, ribose and xylose). The structure of the bis-chelates was affected by the bulk of the DTBS groups and the requiremen... |
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Induction of aldose reductase and xylitol dehydrogenase activities in Candida tenuis CBS 4435.
FEMS Microbiol. Lett. 149(1) , 31-7, (1997) In this study the ability of various sugars and sugar alcohols to induce aldose reductase (xylose reductase) and xylitol dehydrogenase (xylulose reductase) activities in the yeast Candida tenuis was investigated. Both enzyme activities were induced when the o... |
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Substrate specificity of the Bacillus licheniformis lyxose isomerase YdaE and its application in in vitro catalysis for bioproduction of lyxose and glucose by two-step isomerization.
Appl. Environ. Microbiol. 77(10) , 3343-50, (2011) Enzymatic processes are useful for industrially important sugar production, and in vitro two-step isomerization has proven to be an efficient process in utilizing readily available sugar sources. A hypothetical uncharacterized protein encoded by ydaE of Bacil... |
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Synthesis of 4-cyanophenyl and 4-nitrophenyl 2-azido-2-deoxy-1,5-dithio-beta-D-arabino- and -beta-D-lyxopyranosides possessing antithrombotic activity.
Carbohydr. Res. 325(2) , 143-9, (2000) Tri-O-acetyl-5-thio-D-ribopyranosyl bromide was converted into 3,4-di-O-benzoyl-1,5-anhydro-5-thio-D-erythro-pent-1-enitol (3,4-di-O-benzoyl-5-thio-D-ribal), the azidonitration of which afforded an unstable mixture of 2-azido-3,4-di-O-benzoyl-2-deoxy-1-O-nitr... |
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The crystal structure of a lyxose-bridged dimolybdate: a redetermination of the first monosaccharide-metal complex's structure.
Carbohydr. Res. 344(4) , 539-40, (2009) The crystal structure of the first monosaccharide-metal complex ever reported, a beta-D-lyxofuranose-bridged dimolybdate [Taylor, G. E.; Waters, J. M. Tetrahedron Lett.1981, 22, 1277-1278] was re-determined since the original work shows unbalanced charges, an... |