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3',5,5',7-Tetrahydroxyflavanone

CAS# 160436-10-2

3',5,5',7-Tetrahydroxyflavanone

Catalog No. BCN1710----Order now to get a substantial discount!

Product Name & Size Price Stock
3',5,5',7-Tetrahydroxyflavanone: 5mg Please Inquire In Stock
3',5,5',7-Tetrahydroxyflavanone: 10mg Please Inquire In Stock
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3',5,5',7-Tetrahydroxyflavanone: 50mg Please Inquire Please Inquire
3',5,5',7-Tetrahydroxyflavanone: 100mg Please Inquire Please Inquire
3',5,5',7-Tetrahydroxyflavanone: 200mg Please Inquire Please Inquire
3',5,5',7-Tetrahydroxyflavanone: 500mg Please Inquire Please Inquire
3',5,5',7-Tetrahydroxyflavanone: 1000mg Please Inquire Please Inquire

Quality Control of 3',5,5',7-Tetrahydroxyflavanone

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Chemical structure

3',5,5',7-Tetrahydroxyflavanone

3D structure

Chemical Properties of 3',5,5',7-Tetrahydroxyflavanone

Cas No. 160436-10-2 SDF Download SDF
PubChem ID 52945930 Appearance Powder
Formula C15H12O6 M.Wt 288.3
Type of Compound Flavonoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (2S)-2-(3,5-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one
SMILES C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=CC(=C3)O)O
Standard InChIKey AYHOUUNTAVCXBN-ZDUSSCGKSA-N
Standard InChI InChI=1S/C15H12O6/c16-8-1-7(2-9(17)3-8)13-6-12(20)15-11(19)4-10(18)5-14(15)21-13/h1-5,13,16-19H,6H2/t13-/m0/s1
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.

Source of 3',5,5',7-Tetrahydroxyflavanone

The herb of Ilex centrochinensis.

Biological Activity of 3',5,5',7-Tetrahydroxyflavanone

Description1. 5,7,3',5'-Tetrahydroxyflavanone has inhibitory effects on HIV-1 reverse transcriptase (RT)-associated RNase H function, it may have antiviral activity against HIV-1. 2. 5,7,3',5'-Tetrahydroxyflavanone has anti-inflammatory properties, it can inhibit nitric oxide (NO) production with IC50 values of 18.5 uM, the inhibitory effect is accompanied by dose-dependent decreases in LPS-induced nitric oxide synthase (iNOS) in RAW 264.7 cells.
TargetsHIV | NO | NOS

3',5,5',7-Tetrahydroxyflavanone Dilution Calculator

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3',5,5',7-Tetrahydroxyflavanone Molarity Calculator

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Preparing Stock Solutions of 3',5,5',7-Tetrahydroxyflavanone

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.4686 mL 17.343 mL 34.6861 mL 69.3722 mL 86.7152 mL
5 mM 0.6937 mL 3.4686 mL 6.9372 mL 13.8744 mL 17.343 mL
10 mM 0.3469 mL 1.7343 mL 3.4686 mL 6.9372 mL 8.6715 mL
50 mM 0.0694 mL 0.3469 mL 0.6937 mL 1.3874 mL 1.7343 mL
100 mM 0.0347 mL 0.1734 mL 0.3469 mL 0.6937 mL 0.8672 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 3',5,5',7-Tetrahydroxyflavanone

[Studies on chemical constituents of Cercis chinensis].[Pubmed:17260796]

Zhongguo Zhong Yao Za Zhi. 2006 Nov;31(21):1795-7.

OBJECTIVE: To study the chemical constituents from the aerial part of Cercis chinensis. METHOD: The constituents of C. chinensis were separated with various chromatographic techniques and their structures were elucidated by means of spectral analysis and physico-chemical properties. RESULT: Nine compounds were isolated from C. chinensis. They were identified as 3-O-methylquercetin (1), quercetin (2), (2R,3R)-3, 5, 7, 3', 5'-pentahydroxyflavan (3), 3', 5, 5', 7-tetrahydroxyflavanone (4), [+]-taxifolin (5), (2R)-naringenin (6), friedelin (7), beta-sitosterol (8), daucosterin (9). CONCLUSION: compounds 1 and 3-7 were isolated from the genus Cercis for the first time.

Hypericum hircinum L. components as new single-molecule inhibitors of both HIV-1 reverse transcriptase-associated DNA polymerase and ribonuclease H activities.[Pubmed:23821410]

Pathog Dis. 2013 Aug;68(3):116-24.

Among HIV-1 reverse transcriptase (RT)-associated functions, DNA polymerase and Ribonuclease H (RNase H) are both essential for HIV replication and excellent targets for drug development. While all RT inhibitors approved for therapy target the DNA polymerase activity, there is the pressing need for new RT inhibitors possibly targeting the RNase H function. In the last 20 years, many natural substances have shown antiviral activity against HIV-1, but only a few against the RNase H function. In this study, we have tested the ethanolic extracts obtained by the Hypericum hircinum L. (Hypericaceae) growing in Sardinia (Italy) on the HIV-1 RT-associated RNase H function and found that they have inhibitory effects. Active extracts were fractionated up to obtain the main components that have been isolated, tested, and identified to be betulinic acid, shikimic acid, chlorogenic acid, quercetin, 5,7,3',5'-tetrahydroxyflavanone, and 5,7,3',5'-tetrahydroxyflavanone 7-O-glucoside. Betulinic acid and 5,7,3',5'-tetrahydroxyflavanone 7-O-glucoside were active on both RT-associated activities, and betulinic acid was also active on HIV-1 mutant RTs resistant to efavirenz. Overall, our results suggest that some of these compounds inhibit the HIV-1 RT binding to an allosteric site previously described for other natural compounds and are potential leads for further drug development of a single molecules having dual inhibitory activity.

Anti-inflammatory compounds from Ampelopsis cantoniensis.[Pubmed:25924510]

Nat Prod Commun. 2015 Mar;10(3):383-5.

Many natural products have been shown to have an inhibitory effect on nitric oxide (NO), and are used as chemotherapy agents for inflammation disease. The current study was designed to evaluate the anti-inflammatory activity of chemical components from the leaves of Ampelopsis cantoniensis. Sixteen compounds (1-16) were isolated and identified. Phloretin (5) and 5,7,3',5'-tetrahydroxyflavanone (16) inhibited nitric oxide (NO) production with IC50 values of 5.2, and 18.5 muM, respectively. The inhibitory effect of compounds 5 and 16 were accompanied by dose-dependent decreases in LPS-induced nitric oxide synthase (iNOS) in RAW 264.7 cells, respectively. This study investigated the significant anti-inflammatory properties of isolated compounds from the leaves of A. cantoniensis for the first time. The findings demonstrate that A. cantoniensis could be used beneficially in the treatment of inflammation disease.

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