Stelleranol

CAS# 795308-62-2

Stelleranol

2D Structure

Catalog No. BCN8014----Order now to get a substantial discount!

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Stelleranol: 5mg $1024 In Stock
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Quality Control of Stelleranol

3D structure

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Stelleranol

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Chemical Properties of Stelleranol

Cas No. 795308-62-2 SDF Download SDF
PubChem ID 131676072 Appearance Powder
Formula C30H22O11 M.Wt 558.49
Type of Compound Flavonoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
SMILES C1C(C(OC2=C1C(=O)C=C3C24C(C(O3)C5=CC=C(C=C5)O)(C(=O)C6=C(C=C(C=C6O4)O)O)O)C7=CC=C(C=C7)O)O
Standard InChIKey JTLAASAWWOBQSW-SUCIVVAUSA-N
Standard InChI InChI=1S/C30H22O11/c31-15-5-1-13(2-6-15)25-21(36)11-18-19(34)12-23-30(28(18)40-25)29(38,27(39-23)14-3-7-16(32)8-4-14)26(37)24-20(35)9-17(33)10-22(24)41-30/h1-10,12,21,25,27,31-33,35-36,38H,11H2/t21-,25-,27?,29?,30?/m1/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 Stelleranol

The roots of Stellera chamaejasme

Biological Activity of Stelleranol

Description1. Stelleranol shows potent in vitro antiviral activity against respiratory syncytial virus (RSV).
TargetsAntifection

Stelleranol Dilution Calculator

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Stelleranol Molarity Calculator

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Preparing Stock Solutions of Stelleranol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.7905 mL 8.9527 mL 17.9054 mL 35.8108 mL 44.7636 mL
5 mM 0.3581 mL 1.7905 mL 3.5811 mL 7.1622 mL 8.9527 mL
10 mM 0.1791 mL 0.8953 mL 1.7905 mL 3.5811 mL 4.4764 mL
50 mM 0.0358 mL 0.1791 mL 0.3581 mL 0.7162 mL 0.8953 mL
100 mM 0.0179 mL 0.0895 mL 0.1791 mL 0.3581 mL 0.4476 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 Stelleranol

Antiviral biflavonoids from Radix Wikstroemiae (Liaogewanggen).[Pubmed:20565950]

Chin Med. 2010 Jun 21;5:23.

BACKGROUND: Radix Wikstroemiae is a common Chinese herbal medicine. The ethyl acetate fraction of the ethanolic extract of W. indica possesses potent in vitro antiviral activity against respiratory syncytial virus (RSV). This study aims to identify the antiviral components of the active fraction. METHODS: The active fraction of the Radix Wikstroemiae extract was isolated with chromatographic methods such as silica gel, Sephadex LH-20 and semi-preparative high performance liquid chromatography (HPLC) columns. The structures of the isolated compounds were determined based on spectroscopic analyses. The in vitro antiviral activity of the compounds against RSV was tested with the cytopathic effect (CPE) reduction assay and the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) method. RESULTS: Four biflavonoids, namely neochamaejasmin B, genkwanol B, genkwanol C and Stelleranol, were isolated and characterized. Genkwanol B, genkwanol C and Stelleranol, which are stereo isomers of spirobiflavonoids, showed potent anti-RSV activity whereas neochamaejasmin B did not. CONCLUSION: Neochamaejasmin B, genkwanol B, genkwanol C and Stelleranol were isolated from Radix Wikstroemiae and the complete absolute configurations of five chiral carbons in Stelleranol were substantiated for the first time. Furthermore, the anti-RSV activity of genkwanol B, genkwanol C and Stelleranol was reported for the first time.

Chemical Constituents from the Roots, Stems and Leaves of Diplomorpha sikokiana.[Pubmed:27396196]

Nat Prod Commun. 2016 Apr;11(4):475-6.

Four diarylpentanoids (1-4), two phenylpropanoids (5-6), three biflavonoids (7-9), two lignans (10-11) and a coumarin (12) were isolated from the roots of Diploniorpha sikokiana (Franchet & Savatier) Honda (Family: Thymelaeaceae). Similarly, two phenylpropanoids (5-6), five biflavonoids (7-9, 13, 14), three lignans (11, 15, 16), a flavonoid (17) and two coumarins (12, 18) were isolated from the stems, and five flavonoids (17, 19-22) from the leaves. Among them, 1,5-diphenyl-l-pentanone (1), 1,5-diphenyl-2-penten-l-one (2), 3(S)-hydroxy-1,5-diphenylpentane (3), Stelleranol (8), (-)-syringaresinol (10), (-)-pinoresinol 4,4'-di-O-beta-D-glucopyranoside (11), apiosylskimmin (12), syringaresinol 4-O-beta-D-glucopyranoside (16), quercetin 3-O-alpha-L-rhamnopyranoside (19), kaempferol 3-0-alpha-L-rhamnopyranoside (20) and tiliroside (21) were isolated for the first time from D. sikokiana.

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