Isoquercitrin structure
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Common Name | Isoquercitrin | ||
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CAS Number | 482-35-9 | Molecular Weight | 464.376 | |
Density | 1.9±0.1 g/cm3 | Boiling Point | 872.6±65.0 °C at 760 mmHg | |
Molecular Formula | C21H20O12 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 307.5±27.8 °C |
Use of IsoquercitrinQuercetin-3-glucoside is a naturally occurring polyphenol that has antioxidant, anti-proliferative, and anti-inflammatory properties.Quercetin-3-glucoside alleviates ethanol-induced hepatotoxicity, oxidative stress, and inflammatory responses via the Nrf2/ARE antioxidant signaling pathway[1].Quercetin-3-glucoside regulates the expression of nitric oxide synthase 2 (NO2) via modulating the nuclear factor-κB (NF-κB) transcription regulation system. Quercetin-3-glucoside has high bioavailability and low toxicity, is a promising candidate agent to prevent birth defects in diabetic pregnancies[2]. |
Name | 3,3′,4′,5,7-Pentahydroxyflavone 3-β-glucoside, Isoquercitrin, Quercetin 3-β-D-glucoside |
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Synonym | More Synonyms |
Description | Quercetin-3-glucoside is a naturally occurring polyphenol that has antioxidant, anti-proliferative, and anti-inflammatory properties.Quercetin-3-glucoside alleviates ethanol-induced hepatotoxicity, oxidative stress, and inflammatory responses via the Nrf2/ARE antioxidant signaling pathway[1].Quercetin-3-glucoside regulates the expression of nitric oxide synthase 2 (NO2) via modulating the nuclear factor-κB (NF-κB) transcription regulation system. Quercetin-3-glucoside has high bioavailability and low toxicity, is a promising candidate agent to prevent birth defects in diabetic pregnancies[2]. |
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Related Catalog | |
In Vitro | Quercetin-3-glucoside (5-20 μM; 24 hours) substantially reduces ethanol-induced cytotoxicity , protects hepatic cells against ethanol‐stimulated liver injury[1].Quercetin-3-glucoside (10 μM; pre-treat 1 hour) dramatically downregulates the levels of ethanol-induced iNOS protein expression in HepG2 cells[1]. Cell Viability Assay[1] Cell Line: HepG2 cells Concentration: 5 μM, 10 μM, 20 μM Incubation Time: 24 hours Result: Caused significantly enhanced cell viability as positive controls. Western Blot Analysis[1] Cell Line: HepG2 cells Concentration: 10 μM Incubation Time: 1 hour Result: Decreased ethanol‐ induced iNOS protein expression. |
References |
Density | 1.9±0.1 g/cm3 |
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Boiling Point | 872.6±65.0 °C at 760 mmHg |
Molecular Formula | C21H20O12 |
Molecular Weight | 464.376 |
Flash Point | 307.5±27.8 °C |
Exact Mass | 464.095490 |
PSA | 210.51000 |
LogP | 1.75 |
Vapour Pressure | 0.0±0.3 mmHg at 25°C |
Index of Refraction | 1.803 |
Storage condition | −20°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi: Irritant; |
Safety Phrases | 24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | LK8960000 |
Precursor 5 | |
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DownStream 10 | |
A nicotinic receptor-mediated anti-inflammatory effect of the flavonoid rhamnetin in BV2 microglia.
Fitoterapia 98 , 11-21, (2014) The alpha7 nicotinic acetylcholine receptor (nAChR) is a potential target in neuroinflammation. Screening a plant extract library identified Solidago nemoralis as containing methyl-quercetin derivativ... |
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New Polyphenols Identified in Artemisiae abrotani herba Extract.
Molecules 20 , 11063-75, (2015) Artemisia abrotanum L. ("southernwood") belongs to the Artemisia genus and it is used in traditional medicine for the treatment of a variety of illnesses. Scarce data is available on the chemical comp... |
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Comparative Studies on Polyphenolic Composition, Antioxidant and Diuretic Effects of Nigella sativa L. (Black Cumin) and Nigella damascena L. (Lady-in-a-Mist) Seeds.
Molecules 20 , 9560-74, (2015) This study was performed to evaluate the phenolic profile, antioxidant and diuretic effects of black cumin and lady-in-a-mist seeds. In the phenolic profile, differences between the two species are si... |
Quercetin 3-O-β-glucoside |
trifoliin |
quercetin 3-O-β-D-glucopyranoside |
Quercetin 3β-O-glucoside |
Quercetin 3-β-glucoside |
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl β-D-glucopyranoside |
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one |
Quercetin 3-β-D-glucoside |
3-O-β-D-Glucopyranosylquercetin |
Quercetin glucoside |
Quercetin-3-O-β-D-glucoside |
Quercetin-3-O-β-glucopyranoside |
Isoquercetrin |
Quercetin 3-O-glucoside |
Quercetin 3-D-glucoside |
Isoquercitrin |
isoquercetin |
quercetin 3-O-β-D-glucoside |
Hirsutrin |
isotrifoliin |
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-3-(β-D-glucopyranosyloxy)-5,7-dihydroxy- |
Quercetin 3-glucoside |
Quercetin-3-β-glucopyranoside |
Quercetin-3-O-glucoside |
Quercetin 3-β-O-glucoside |
Quercetin 3-O-glucopyranoside |