10257-35-9

Basic information

• Product Name: Lyxopyranose (7CI,8CI,9CI)
• Synonyms: Lyxopyranose (7CI,8CI,9CI)
• CAS NO: 10257-35-9
• Molecular Formula: C₅H₁₀O₅
• Molecular Weight: 150.1299
• Product Categories: CARBOHYDRATE
• Mol File: 10257-35-9.mol
• Article Data: 279

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Lyxopyranose (7CI,8CI,9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Lyxopyranose (7CI,8CI,9CI)(10257-35-9)
• EPA Substance Registry System: Lyxopyranose (7CI,8CI,9CI)(10257-35-9)

Safety Data

• Hazardous Substances Data: 10257-35-9(Hazardous Substances Data)

Upstream product

• 65604-80-0 mixture of 3-O-<α-L-rhamnopyranosyl-(1->2)><β-D-xylopyranosyl(1->3)>-β-D-glucopyranosides of diosgenin and yamogenin 
• 105798-62-7 alliofuroside A 
• 105822-00-2 22-O-methyl ether of alliofuroside A 
• 1357111-69-3 2,6-dimethoxy-p-hydroquinone 1-O-β-D-xylopyranosyl-(1->6)-β-D-glucopyranoside 
• 532-20-7 D-lyxose 
• 67-56-1 methanol 
• 552-71-6 D-(+)-xylobiose 
• 1386988-87-9 (3β,20S)-3,20,21-trihydroxydammar-24-ene 3-O-[α-L-rhamnopyranosyl-(1-2)]-[β-D-xylopyranosyl-(1-3)]-α-L-arabinopyranoside 
• 1386988-84-6 (3β,20S,23R)-3,20,23-trihydroxydammar-24-en-21-oic acid-21,23-lactone 3-O-[α-L-rhamnopyranosyl-(1-2)]-[β-D-xylopyranosyl-(1-3)]-α-L-arabinopyranoside 
• 1386988-85-7 (3β,20S,23S)-3,20,23-trihydroxydammar-24-en-21-oic acid-21,23-lactone 3-O-[α-L-rhamnopyranosyl-(1-2)]-[β-D-xylopyranosyl-(1-3)]-α-L-arabinopyranoside 
• 1386988-86-8 (20S,23S)-3β,20-dihydroxydammar-24-en-21-oic acid-21,23-lactone-3-O-[β-D-xylopyranosyl(1→3)]-β-D-glucopyranoside 
• 862286-45-1 (3β,20S,23S)-3,20,23-trihydroxydammar-24-en-21-oic acid-21,23-lactone 3-O-[α-L-rhamnopyranosyl-(1→2)]-[β-D-xylopyranosyl-(1→3)]-β-D-6-O-acetylglucopyranoside 
• 862286-49-5 (3β,20S,23S)-3,20,23-trihydroxydammar-24-en-21-oic acid-21,23-lactone 3-O-[α-L-rhamnopyranosyl-(1→2)]-[β-D-xylopyranosyl-(1→3)]-β-D-glucopyranoside 
• 1383540-06-4 26-O-β-D-glucopyranosyl-(25R)-furost-5-en-3β,20α,26-triol 3-O-β-D-xylopyranosyl(1->4)-[α-L-rhamnopyranosyl(1->2)]-β-D-glucopyranoside 

Downstream Products

• 91-09-8 methyl xyloside 
• 612-05-5 methyl-β-D-xylopyranoside 
• 91-09-8 methyl-α-D-xylopyranoside 
• 62410-08-6 5-deoxy-1,2-O-isopropylidene-α-D-xylohexofuranose 
• 76222-63-4 3,5-O-isopropylidene-D-xylofuranose 
• 13039-94-6 2,3,4,5-di-O-isopropylidene-D-xylose aldehyde 
• 2001-96-9 p-nitrophenyl β-D-xylopyranoside 
• 25217-96-3 p-Acetyl-phenyl-β-D-xylopyranosid 
• 161879-31-8 1-(3-methoxy-4-β-D-xylopyranosyloxy-phenyl)-ethanone 
• 98-01-1 furfural 
• 141-46-8 Glycolaldehyde 
• 116-09-6 hydroxy-2-propanone 
• 532-20-7 D-lyxose 
• 78-98-8 2-oxopropanal 

Relevant articles and documents

New triterpenoid saponin from the stems of Albizia adianthifolia (Schumach.) W.Wight

As part of our continuing study of apoptosis-inducing saponins from Cameroonian Albizia genus, one new triterpenoid saponin, named adianthifolioside J (1), together with the known gummiferaoside E (2), were isolated from Albizia adianthifolia stems. The s

New flavonoid glycosides from Xanthium strumarium with their protein tyrosine phosphatase 1B inhibitory activity

Two new flavonoid glycosides named 6-hydroxy-3-methoxy-apigenin 7-O-α-?-rhamnopyranoside (1) and 3-hydroxyl-apigenin 8-C-β-?-xylopyranoside (2), along with five known compounds (3-7), were isolated from Xanthium strumarium. Their structures were elucidate

Mimonoside D: a new triterpenoid saponin from Mimosa diplotricha Sauvalle (Fabaceae)

A new triterpenoid saponin (Mimonoside D: 3-O-α-L-arabinopyranosyl-3β-hydroxyolean-12-en-28-oic acid 28-O-β-D-xylopyranosyl-(1→2)-β-D- glucopyranoside ester (1)) was isolated from the aerial parts of Mimosa diplotricha Sauvalle together with nine known compounds: 7,4′-dihydroxyflavone (2), kaempferol (3), lupeol (4), betulinic acid (5), β-sitosterol (6), β-sitosterol-3-O-β-D-glucopyranoside (7), lutein (8), 5,2′-dihydroxy-7,4′,5′-trimethoxyflavone (9) and vitexin (10). Their structures were elucidated on the basis of spectroscopic (1D and 2D nuclear magnetic resonance) and high-resolution mass spectrometric data as well as by comparison of their spectral data with those of related compounds. Compounds 2, 7 and 8 had already been isolated from M. diplotricha, while compounds 3, 4, 5 and 6 have been isolated from other Mimosa species. Compound 2 moderately inhibited Proteus mirabilis (MIC = 32μg/mL), weakly inhibited Pseudomonas aeruginosa (MIC = 64μg/mL) and very weakly inhibited Staphylococcus aureus (MIC = 128μg/mL) and Enterococus faecalis (MIC = 128μg/mL).