130606-21-2

Basic information

• Product Name: alpha-Lyxopyranose (9CI)
• Synonyms: alpha-Lyxopyranose (9CI)
• CAS NO: 130606-21-2
• Molecular Formula: C₅H₁₀O₅
• Molecular Weight: 150.1299
• Product Categories: CARBOHYDRATE
• Mol File: 130606-21-2.mol
• Article Data: 279

Chemical Properties

• Appearance: /
• CAS DataBase Reference: alpha-Lyxopyranose (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: alpha-Lyxopyranose (9CI)(130606-21-2)
• EPA Substance Registry System: alpha-Lyxopyranose (9CI)(130606-21-2)

Safety Data

• Hazardous Substances Data: 130606-21-2(Hazardous Substances Data)

Upstream product

• 552-71-6 D-(+)-xylobiose 
• 67-63-0 isopropyl alcohol 
• 111-27-3 hexan-1-ol 
• 15596-26-6 3-O-β-D-xylopyranosylstrophanthidin 
• 99656-38-9 bis(N-D-xylosyl-3-aminopropionato)nickel(II)*2(water) 
• 1227373-24-1 3-O-[α-L-rhamnopyranosyl-(1->2)-β-D-xylopyranosyl]-6-O-β-D-glucopyranosyl-24-O-α-(4'-O-acetyl)-L-arabinopyranosyl-16-O-acetyl-3β,6α,16β,24(S),25-pentahydroxycycloartane 
• 109742-55-4 trachelosperoside B-2 
• 109742-54-3 trachelosperoside C-1 
• 84976-26-1 O-<5-O-(trans-feruloyl)-α-L-arabinofuranosyl>-(1<*>3)-O-β-D-xylopyranosyl-(1<*>4)-D-xylopyranose 
• 68385-35-3 herbacetin 8-(3''-O-acetylxyloside) 
• 76729-70-9 echinocystic acid-3-O-<β-D-xylopyranosyl(1->2)-α-L-arabinopyranosyl(1->6)-β-D-glucopyranoside>-28-O-<β-D-xylopyranosyl(1->3)-β-D-xylopyranosyl(1->4)-α-L-rhamnopyranosyl(1->2)><α-L-rhamnopyranosyl(1->6)>-β-D-glucopyranoside 
• 75410-53-6 3-O-{(3-O-methyl-β-D-glucopyranosyl)-(1→3)-(β-D-glucopyranosyl)-(1→4)-(β-D-quinopyranosyl)-(1→2)-4-O-sodium sulfate-β-D-xylopyranosyl}holosta-9(11)-ene-3β,12α,17α-triol 
• 76729-67-4 hederagenin 3-O-β-D-glucopyranosyl-(1-4)-β-D-glucopyranosyl-(1-4)-β-D-xylopyranosyl-(1-3)-α-L-rhamnopyranosyl-(1-2)-α-L-arabinopyranoside 
• 75410-52-5 echinoside B 

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

Ursane-type triterpene oligoglycosides with anti-hepatosteatosis and anti-hyperlipidemic activity from the leaves of Ilex paraguariensis A. St.-Hil.

The methanol extract from the leaves of Ilex paraguariensis A. St.-Hil. (Aquifoliaceae), popularly known as mate, maté, or yerba maté, inhibits the intracellular triglyceride accumulation in HepG2 cells and suppresses the plasma triglyceride elevation in olive oil-treated mice. Three new triterpene saponins, termed mateosides I (1), II (2), and III (3), were isolated from the extract along with 29 known compounds. The structures of 1–3 were elucidated based on chemical and spectroscopic evidence. Among the isolates, principal saponin constituents, 2 and matesaponins 1 (7) and 2 (9), potently inhibited the triglyceride accumulation in HepG2 cells simultaneously treated with oleic acid and high glucose. In vivo assay of the methanol extract of I. paraguariensis revealed that 7 and 9 showed anti-hyperlipidemic activities in olive oil-treated mice. These results suggested that the saponin constituents of I. paraguariensis could be valuable bioactive marker for the anti-obesogenic activity. Graphical abstract: [Figure not available: see fulltext.]

Protective effects of four new saponins from Gynostemma pentaphyllum against hydrogen peroxide-induced neurotoxicity in SH-SY5Y cells

Gynostemma pentaphyllum has been used as a medicine-food homologious health product in China for a long time. This research aimed to isolate and identify its active compounds with protective effects against hydrogen peroxide induced SH-SY5Y cell death. Four new dammarane-type saponins were isolated from G. pentaphyllum using various chromatographic methods. They were identified as gypenoside S1 (1), gypenoside S3 (2), gypenoside S2 (3) and gypenoside S4 (4), respectively by HRESIMS and NMR spectra. Their cytotoxic activity was evaluated against three human cancer cell lines, A549 (lung), HepG2 (liver), SH-SY5Y (nerve), by MTT method. They showed low cytotoxicities with the IC50 values of more than 100 μM on three cancer cell lines. However, they appeared protective effects against hydrogen peroxide induced SH-SY5Y cell death in a dose-dependent manner. They recovered cell viability more than 69% at the concentration of 20 μM from 66%, while as vitamin C to 67%. Compound 3 and 4 recovered more than 79% at 100 μM. The present study suggests that G. pentaphyllum has antioxidative potential and the saponins from G. pentaphyllum are considered as the active compounds with safe and neuroprotecitve effect.