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Apigenin-7-diglucuronide

CAS# 74696-01-8

Apigenin-7-diglucuronide

2D Structure

Catalog No. BCX0667----Order now to get a substantial discount!

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Apigenin-7-diglucuronide: 5mg Please Inquire In Stock
Apigenin-7-diglucuronide: 10mg Please Inquire In Stock
Apigenin-7-diglucuronide: 20mg Please Inquire Please Inquire
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Apigenin-7-diglucuronide: 1000mg Please Inquire Please Inquire

Quality Control of Apigenin-7-diglucuronide

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Apigenin-7-diglucuronide

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Chemical Properties of Apigenin-7-diglucuronide

Cas No. 74696-01-8 SDF Download SDF
PubChem ID N/A Appearance Powder
Formula C27H26O17 M.Wt 622.49
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Apigenin-7-diglucuronide Dilution Calculator

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Apigenin-7-diglucuronide Molarity Calculator

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Preparing Stock Solutions of Apigenin-7-diglucuronide

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.6065 mL 8.0323 mL 16.0645 mL 32.129 mL 40.1613 mL
5 mM 0.3213 mL 1.6065 mL 3.2129 mL 6.4258 mL 8.0323 mL
10 mM 0.1606 mL 0.8032 mL 1.6065 mL 3.2129 mL 4.0161 mL
50 mM 0.0321 mL 0.1606 mL 0.3213 mL 0.6426 mL 0.8032 mL
100 mM 0.0161 mL 0.0803 mL 0.1606 mL 0.3213 mL 0.4016 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on Apigenin-7-diglucuronide

Apigenin-7-diglucuronide protects retinas against bright light-induced photoreceptor degeneration through the inhibition of retinal oxidative stress and inflammation.[Pubmed:28336272]

Brain Res. 2017 May 15;1663:141-150.

Vision impairment in retinal degenerative diseases such as age-related macular degeneration is primarily associated with photoreceptor degeneration, in which oxidative stress and inflammatory responses are mechanistically involved as central players. Therapies with photoreceptor protective properties remain to be developed. Apigenin-7-diglucuronide (A7DG), a flavonoid glycoside, is present in an assortment of medicinal plants with anti-inflammatory or ant-oxidant activities. However, the pharmacological significance of A7DG remains unknown in vivo. The current study isolated A7DG from Glechoma longituba (Nakai) Kuprian and investigated the retinal protective effect A7DG in mice characterized by bright light-induced photoreceptor degeneration. The results showed that A7DG treatment led to remarkable photoreceptor protection in bright light-exposed BALB/c mice. Moreover, A7DG treatment alleviated photoreceptor apoptosis, mitigated oxidative stress, suppressed reactive gliosis and microglial activation and attenuated the expression of proinflammatory genes in bright light-exposed retinas. The results demonstrated for the first time remarkable photoreceptor protective activities of A7DG in vivo. Inhibition of bright light-induced retinal oxidative stress and retinal inflammatory responses was associated with the retinal protection conferred by A7DG. The work here warrants further evaluation of A7DG as a pharmacological candidate for the treatment of vision-threatening retinal degenerative disorders. Moreover, given the general implication of oxidative stress and inflammation in the pathogenesis of neurodegeneration, A7DG could be further tested for the treatment of other neurodegenerative disorders.

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