Rutarensin

CAS# 119179-04-3

Rutarensin

2D Structure

Catalog No. BCN0216----Order now to get a substantial discount!

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Rutarensin: 5mg $265 In Stock
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Quality Control of Rutarensin

3D structure

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Rutarensin

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Chemical Properties of Rutarensin

Cas No. 119179-04-3 SDF Download SDF
PubChem ID 11958880 Appearance Powder
Formula C31H30O16 M.Wt 658.56
Type of Compound Coumarins Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 3-hydroxy-3-methyl-5-oxo-5-[[3,4,5-trihydroxy-6-[6-methoxy-2-oxo-3-(2-oxochromen-7-yl)oxychromen-7-yl]oxyoxan-2-yl]methoxy]pentanoic acid
SMILES CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C3C=C(C(=O)OC3=C2)OC4=CC5=C(C=C4)C=CC(=O)O5)OC)O)O)O)O
Standard InChIKey ZTLZGWDERZVHNS-UHFFFAOYSA-N
Standard InChI InChI=1S/C31H30O16/c1-31(40,11-23(32)33)12-25(35)42-13-22-26(36)27(37)28(38)30(47-22)46-20-10-18-15(7-19(20)41-2)8-21(29(39)45-18)43-16-5-3-14-4-6-24(34)44-17(14)9-16/h3-10,22,26-28,30,36-38,40H,11-13H2,1-2H3,(H,32,33)
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 Rutarensin

The herbs of Wikstroemia indica

Rutarensin Dilution Calculator

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Rutarensin Molarity Calculator

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Preparing Stock Solutions of Rutarensin

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.5185 mL 7.5923 mL 15.1846 mL 30.3693 mL 37.9616 mL
5 mM 0.3037 mL 1.5185 mL 3.0369 mL 6.0739 mL 7.5923 mL
10 mM 0.1518 mL 0.7592 mL 1.5185 mL 3.0369 mL 3.7962 mL
50 mM 0.0304 mL 0.1518 mL 0.3037 mL 0.6074 mL 0.7592 mL
100 mM 0.0152 mL 0.0759 mL 0.1518 mL 0.3037 mL 0.3796 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 Rutarensin

Phenolic compounds from the aerial parts of Diplomorpha canescens.[Pubmed:22466741]

Chem Pharm Bull (Tokyo). 2012;60(4):554-6.

One new C-methyl flavanone glucoside, farrerol 4'-O-beta-D-glucopyranoside (1) was isolated from the aerial parts of Diplomorpha canescens (MEISN.) C. A. MEYER. Fourteen known phenolic compounds such as farrerol (2), luteolin 7-methyl ether 5-O-beta-D-glucopyranoside (3), (-)-pinoresinol (4), (-)-lariciresinol (5), (-)-dihydrosesamin (6), (+/-)-dehydrodiconiferyl alcohol (7), Rutarensin (8), umbelliferone (9), coniferyl aldehyde (10), sinapyl aldehyde (11), p-coumaric acid methyl ester (12), p-hydroxybenzaldehyde (13), p-hydroxyacetophenone (14) and syringaldehyde (15) were also isolated for the first time from this plant. Structure of 1 was determined on the basis of spectroscopic data including two dimensional (2D)-NMR, circular dichroism (CD) and by the application of Klyne's rule.

Bioactive coumarins from Boenninghausenia sessilicarpa.[Pubmed:17365191]

J Asian Nat Prod Res. 2007 Jan-Feb;9(1):59-65.

Bioassay guided fractionation of Boenninghausenia sessilicarpa (Rutaceae) resulted in the isolation of a new dimeric coumarin glucoside 9'-methoxyl Rutarensin (1) and a cytotoxic compound rutamarin (4), as well as an antivirus component leptodactylone (8), together with six known coumarins. Their structures were elucidated by 1D- and 2D NMR spectroscopy and ESI-MS analyses, respectively. Rutamarin (4) showed significant inhibitory activities against A-549, Bel-7402, HepG-2 and HCT-8 tumour cell lines with IC50s of 1.318, 2.082, 2.306 and 2.497 microg/ml. In addition, leptodactylone (8) showed potent protective activity on cells infected by SARS-CoV with ratio of 60% at 100 microg/ml.

A new biscoumarin glucoside ester from Ruta chalepensis cell cultures.[Pubmed:17265302]

Planta Med. 1988 Oct;54(5):398-400.

The investigation of a plant cell culture of RUTA CHALEPENSIS L. yielded three compounds: isorutarin, rutacridone, and Rutarensin, a so far unknown ester of daphnoretin glucoside ("daphnorin"), as well as 3-hydroxy-3-methylglutaric acid.

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