CAS 10257-34-8 | D-Lyxopyranose | CAS Number 10257-34-8

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10257-34-8 | D-Lyxopyranose

CAS No: 10257-34-8 Catalog No: AG0007R7 MDL No:

Product Description

Catalog Number:

AG0007R7

Chemical Name:

D-Lyxopyranose

CAS Number:

10257-34-8

Molecular Formula:

C5H10O5

Molecular Weight:

150.1299

IUPAC Name:

(3S,4S,5R)-oxane-2,3,4,5-tetrol

InChI:

InChI=1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2/t2-,3+,4+,5?/m1/s1

InChI Key:

SRBFZHDQGSBBOR-AGQMPKSLSA-N

SMILES:

O[C@@H]1COC([C@H]([C@H]1O)O)O

Properties

Complexity:

117

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

150.053g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

150.13g/mol

Monoisotopic Mass:

150.053g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

90.2A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

-2.5

Literature

Title	Journal
Characterization of a recombinant thermostable D-lyxose isomerase from Dictyoglomus turgidum that produces D-lyxose from D-xylulose.	Biotechnology letters 20120601
Broadband dielectric spectroscopy and calorimetric investigations of D-lyxose.	Carbohydrate research 20111018
Dibutylsilylene-pentose bis-chelates: on the glycoses' binding sites for strongly Lewis-acidic centres.	Carbohydrate research 20110927
Synthesis of 4-amino-4,5-dideoxy-L-lyxofuranose derivatives and their evaluation as fucosidase inhibitors.	Carbohydrate research 20110715
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 (Basel, Switzerland) 20110714
On the stabilization of ribose by silicate minerals.	Astrobiology 20110301
Characterization of a recombinant thermostable L: -rhamnose isomerase from Thermotoga maritima ATCC 43589 and its application in the production of L-lyxose and L-mannose.	Biotechnology letters 20101201
Substrate specificity of a recombinant D-lyxose isomerase from Serratia proteamaculans that produces D-lyxose and D-mannose.	Letters in applied microbiology 20100901
Substrate specificity of a recombinant D-lyxose isomerase from Providencia stuartii for monosaccharides.	Journal of bioscience and bioengineering 20100701
Asymmetric histidine-catalyzed cross-aldol reactions of enolizable aldehydes: access to defined configured quaternary stereogenic centers.	Journal of the American Chemical Society 20091125
Complexation behavior of mono- and disaccharides by the vinylbenzeneboronic acid-divinylbenzene copolymer resins packed in a high-performance liquid chromatographic column.	Journal of chromatography. A 20091030
The crystal structure of a lyxose-bridged dimolybdate: a redetermination of the first monosaccharide-metal complex's structure.	Carbohydrate research 20090310
Synthesis of 2-deoxy-D-arabino/lyxo-hexopyranosyl disaccharides.	Carbohydrate research 20080225
Theoretical study on the factors controlling the stability of the borate complexes of ribose, arabinose, lyxose, and xylose.	Chemistry (Weinheim an der Bergstrasse, Germany) 20080101
Crystal structure and solid-state 13C NMR analysis of N-p-nitrophenyl-alpha-D-ribopyranosylamine, N-p-nitrophenyl-alpha-D-xylopyranosylamine, and solid-state 13C NMR analysis of N-p-nitrophenyl-2,3,4-tri-O-acetyl-beta-D-lyxopyranosylamine and N-p-nitrophenyl-2,3,4-tri-O-acetyl-alpha-L-arabinopyranosylamine.	Carbohydrate research 20051212
Genes encoding enzymes responsible for biosynthesis of L-lyxose and attachment of eurekanate during avilamycin biosynthesis.	Chemistry & biology 20051001
Pentopyranosyl oligonucleotide systems. Part 11: Systems with shortened backbones: (D)-beta-ribopyranosyl-(4'-->3')- and (L)-alpha-lyxopyranosyl-(4'-->3')-oligonucleotides.	Bioorganic & medicinal chemistry 20010901
A convenient route to higher sugars by two-carbon chain elongation using Wittig/dihydroxylation reactions.	The Journal of organic chemistry 20010629
Design, synthesis, and antiviral activity of alpha-nucleosides: D- and L-isomers of lyxofuranosyl- and (5-deoxylyxofuranosyl)benzimidazoles.	Journal of medicinal chemistry 19980409
L-lyxose metabolism employs the L-rhamnose pathway in mutant cells of Escherichia coli adapted to grow on L-lyxose.	Journal of bacteriology 19910801