vitexin structure
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Common Name | vitexin | ||
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CAS Number | 3681-93-4 | Molecular Weight | 432.378 | |
Density | 1.7±0.1 g/cm3 | Boiling Point | 767.7±60.0 °C at 760 mmHg | |
Molecular Formula | C21H20O10 | Melting Point | 256-257ºC | |
MSDS | Chinese USA | Flash Point | 273.1±26.4 °C |
Use of vitexinVitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Ficus deltoid and Spirodela polyrhiza. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. |
Name | vitexin |
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Synonym | More Synonyms |
Description | Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Ficus deltoid and Spirodela polyrhiza. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. |
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Related Catalog | |
In Vivo | Vitexin exerts neuroprotective effect against pentylenetetrazole-induced seizures, scopolamine-induced memory impairment, and glutamate-induced neuronal excitotoxicity[1]. |
References |
Density | 1.7±0.1 g/cm3 |
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Boiling Point | 767.7±60.0 °C at 760 mmHg |
Melting Point | 256-257ºC |
Molecular Formula | C21H20O10 |
Molecular Weight | 432.378 |
Flash Point | 273.1±26.4 °C |
Exact Mass | 432.105652 |
PSA | 181.05000 |
LogP | 1.28 |
Vapour Pressure | 0.0±2.7 mmHg at 25°C |
Index of Refraction | 1.743 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xn |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | DJ2984000 |
HS Code | 29389090 |
The identification of a novel SIRT6 modulator from Trigonella foenum-graecum using ligand fishing with protein coated magnetic beads.
J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 968 , 105-11, (2014) SIRT6 is a histone deacetylase that has been proposed as a potential therapeutic target for metabolic disorders and the prevention of age-associated diseases. Thus the identification of compounds that... |
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Activity-guided isolation, identification and quantification of biologically active isomeric compounds from folk medicinal plant Desmodium adscendens using high performance liquid chromatography with diode array detector, mass spectrometry and multidimentional nuclear magnetic resonance spectroscopy.
J. Pharm. Biomed. Anal. 102 , 54-63, (2014) The antioxidant activity of the crude extract (60% ethanol) from the leaves of Desmodium adscendens (Sw.) DC. (Fabaceae) was observed in DPPH, xanthine/xanthine oxidase, lipid peroxydation and neutrop... |
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In vitro and in silico studies to explore structural features of flavonoids for aldehyde oxidase inhibition.
Arch. Pharm. (Weinheim) 347(10) , 738-47, (2014) Aldehyde oxidase (AO), an important enzyme in the biotransformation of drugs and xenobiotics, is inhibited by flavonoids. This enzyme can metabolize both aldehydes and N-heterocycles. In this work, a ... |
4H-1-Benzopyran-4-one, 5,7-dihydroxy-8-β-D-glucopyranosyl-2-(4-hydroxyphenyl)- |
4H-1-Benzopyran-4-one, 5,7-dihydroxy-8-β-D- glucopyranosyl-2-(4-hydroxyphenyl)- |
8-Glucosylapigenin |
vitexin |
Apigenin8-C-glucoside |
8-b-D-Glucopyranosyl-apigenin |
ORIENTOSIDE |
Apigenin 8-C-β-D-glucopyranoside |
Vitxein |
4H-1-Benzopyran-4-one, 8-β-D-glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)- |
5,7-Dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]-4H-chromen-4-one |
D-Glucitol, 1,5-anhydro-1-C-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-8-yl]-, (1S)- |
8-D-Glucosyl-4',5,7-trihydroxyflavone |
8-β-D-Glucopyranosyl-apigenin |
(1S)-1,5-Anhydro-1-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-8-yl]-D-glucitol |
8-β-D-Glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one |
Apigenin 8-C-glucoside |
Apigenin-8-C-glucoside |
4',5,7-trihydroxyflavone-8-C-glucoside |
5,7-Dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]-4H-chromen-4-on |
5,7-Dihydroxy-2-(4-hydroxyphényl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxyméthyl)tétrahydro-2H-pyran-2-yl]-4H-chromén-4-one |