Fraxin structure
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Common Name | Fraxin | ||
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CAS Number | 524-30-1 | Molecular Weight | 370.308 | |
Density | 1.6±0.1 g/cm3 | Boiling Point | 722.2±60.0 °C at 760 mmHg | |
Molecular Formula | C16H18O10 | Melting Point | 205-208ºC | |
MSDS | Chinese USA | Flash Point | 267.1±26.4 °C |
Use of FraxinFraxin isolated from Acer tegmentosum, F. ornus or A. hippocastanum, is a glucoside of fraxetin and reported to exert potent anti-oxidative stress action[1], anti-inflammatory and antimetastatic properties. Fraxin shows its antioxidative effect through inhibition of cyclo AMP phosphodiesterase enzyme[2]. |
Name | fraxin |
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Synonym | More Synonyms |
Description | Fraxin isolated from Acer tegmentosum, F. ornus or A. hippocastanum, is a glucoside of fraxetin and reported to exert potent anti-oxidative stress action[1], anti-inflammatory and antimetastatic properties. Fraxin shows its antioxidative effect through inhibition of cyclo AMP phosphodiesterase enzyme[2]. |
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Related Catalog | |
Target |
Cyclo AMP phosphodiesterase enzyme[2]. |
In Vitro | Fraxin (100 μM) is non-cytotoxic on Hep G2 cells. Fraxin at non-cytotoxic concentrations significantly decreases the t-BHP-induced ROS generation in a dose-dependent manner[1]. Fraxin (0.5 mM) shows free radical scavenging effect at high concentration and cell protective effect against H2O2-mediated oxidative stress[2]. |
In Vivo | Fraxin (50 mg/kg, p.o.) significantly blocks the CCl4-induced elevation of ALT and AST. Fraxin (10 and 50 mg/kg, p.o.) significantly reduces the GSSG levels (1.7±0.3 and 1.5±0.2 nM/g liver, respectively) compared with the GSSG levels of the CCl4-treated group[1]. |
References |
Density | 1.6±0.1 g/cm3 |
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Boiling Point | 722.2±60.0 °C at 760 mmHg |
Melting Point | 205-208ºC |
Molecular Formula | C16H18O10 |
Molecular Weight | 370.308 |
Flash Point | 267.1±26.4 °C |
Exact Mass | 370.089996 |
PSA | 159.05000 |
LogP | -1.93 |
Vapour Pressure | 0.0±2.5 mmHg at 25°C |
Index of Refraction | 1.664 |
Storage condition | 2-8°C |
Hazard Codes | Xi |
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RIDADR | NONH for all modes of transport |
RTECS | DJ3091000 |
Precursor 0 | |
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DownStream 1 | |
Screening for novel quorum-sensing inhibitors to interfere with the formation of Pseudomonas aeruginosa biofilm.
J. Med. Microbiol. 60(Pt 12) , 1827-34, (2011) The objective of this study was to screen for novel quorum-sensing inhibitors (QSIs) from traditional Chinese medicines (TCMs) that inhibit bacterial biofilm formation. Six of 46 active components fou... |
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[Studies on chemical constituents from stem barks of Fraxinus paxiana].
Zhongguo Zhong Yao Za Zhi 33(16) , 1990-3, (2008) To investigate the chemical constituents of Fraxinus paxiana.The chemical constituents were isolated and purified by chromatographic techniques and the structures of the compounds were identified with... |
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[Coumarins from branch of Fraxinus sieboldiana and their antioxidative activity].
Zhongguo Zhong Yao Za Zhi 33(14) , 1708-10, (2008) To investigate the chemical constituents from the branch of Fraxinus sieboldiana, and evaluate their antioxidative activity.The chemical constituents were isolated and purified by chromatographic tech... |
7,8-Dihydroxy-6-methoxycoumarin-8-b-D-glucoside |
7-Hydroxy-6-methoxy-2-oxo-2H-chromen-8-yl β-D-glucopyranoside |
8-(Glucosyloxy)-6-methoxyumbelliferone |
UNII-V7M270Y072 |
2H-1-Benzopyran-2-one, 8-(β-D-glucopyranosyloxy)-7-hydroxy-6-methoxy- |
7-Hydroxy-6-méthoxy-8-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxyméthyl)tétrahydro-2H-pyran-2-yl]oxy}-2H-chromén-2-one |
7-Hydroxy-6-methoxy-8-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}-2H-chromen-2-on |
8-(β-D-Glucopyranosyloxy)-7-hydroxy-6-methoxy-2H-1-benzopyran-2-one |
Fraxin |
8-(b-D-Glucopyranosyloxy)-7-hydroxy-6-methoxy-2H-1-benzopyran-2-one |
Fraxoside |
Fraxetin-8-O-glucoside |
Fraxetin-8-glucoside |
Paviin |
7-Hydroxy-6-methoxy-2-oxo-2H-chromen-8-yl-β-D-glucopyranoside |
Fraxetol 8-glucoside |
7-Hydroxy-6-methoxy-8-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}-2H-chromen-2-one |