Xanthiside

CAS# 866366-86-1

Xanthiside

Catalog No. BCN2545----Order now to get a substantial discount!

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Xanthiside: 5mg $552 In Stock
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Quality Control of Xanthiside

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Chemical structure

Xanthiside

3D structure

Chemical Properties of Xanthiside

Cas No. 866366-86-1 SDF Download SDF
PubChem ID 91466627 Appearance Powder
Formula C17H23NO8S M.Wt 401.4
Type of Compound Miscellaneous Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 8,8-dimethyl-7-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4H-1,4-benzothiazine-3,5-dione
SMILES CC1(C(=CC(=O)C2=C1SCC(=O)N2)COC3C(C(C(C(O3)CO)O)O)O)C
Standard InChIKey AKXSDYSKIVXIJA-JCILWVLBSA-N
Standard InChI InChI=1S/C17H23NO8S/c1-17(2)7(3-8(20)11-15(17)27-6-10(21)18-11)5-25-16-14(24)13(23)12(22)9(4-19)26-16/h3,9,12-14,16,19,22-24H,4-6H2,1-2H3,(H,18,21)/t9-,12-,13+,14-,16-/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 Xanthiside

The fruits of Xanthium sibiricum

Protocol of Xanthiside

Structure Identification
Molecules. 2013 Oct 10;18(10):12464-73.

Four new glycosides from the fruit of Xanthium sibiricum Patr.[Pubmed: 24152669]


METHODS AND RESULTS:
Four new glycosides, namely 3β-norpinan-2-one 3-O-β-d-apiofuranosyl-(1→6)-β-d-glucopyranoside (1), (6Z)-3-hydroxymethyl-7-methylocta-1,6-dien-3-ol 8-O-β-d-glucopyranoside (2), (6E)-3-hydroxymethyl-7-methylocta-1,6-dien-3-ol 8-O-β-d-gluco-pyranoside (3), and 7-[(β-d-apiofuranosyl-(1→6)-β-d-glucopyranosyl)oxymethy]-8,8-dimethyl-4,8-dihydrobenzo[1,4]thiazine-3,5-dione (4), were isolated from the fruits of Xanthium sibiricum Patr together with three known compounds, Xanthiside (5), adenosine (6), and 2,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)-propan-1-one (7).
CONCLUSIONS:
The structures of the new compounds were determined on the basis of detailed spectroscopic analyses.

Nat Prod Res. 2005 Sep;19(6):585-9.

A new heterocyclic glucoside from the fruits of Xanthium pungens.[Pubmed: 16010824]


METHODS AND RESULTS:
A new thiazinedione glucoside, 7-(beta-D-glucopyranosyloxymethyl)-8,8-dimethyl-4,8-dihydrobenzo[1,4]thiazine-3,5-dione (1) and named Xanthiside, was isolated from the methanol extract of the fruits of Xanthium pungens.
CONCLUSIONS:
Its structure was determined by spectroscopic techniques including, IR, CIMS, high-resolution-EIMS, and extensive 400 MHz one- and two-dimensional NMR-analysis (1H, 13C-NMR, DEPT, 1H-1H COSY, HMQC, COLOC, and NOE experiments).

Xanthiside Dilution Calculator

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Xanthiside Molarity Calculator

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Preparing Stock Solutions of Xanthiside

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.4913 mL 12.4564 mL 24.9128 mL 49.8256 mL 62.282 mL
5 mM 0.4983 mL 2.4913 mL 4.9826 mL 9.9651 mL 12.4564 mL
10 mM 0.2491 mL 1.2456 mL 2.4913 mL 4.9826 mL 6.2282 mL
50 mM 0.0498 mL 0.2491 mL 0.4983 mL 0.9965 mL 1.2456 mL
100 mM 0.0249 mL 0.1246 mL 0.2491 mL 0.4983 mL 0.6228 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 Xanthiside

Four new glycosides from the fruit of Xanthium sibiricum Patr.[Pubmed:24152669]

Molecules. 2013 Oct 10;18(10):12464-73.

Four new glycosides, namely 3beta-norpinan-2-one 3-O-beta-d-apiofuranosyl-(1-->6)-beta-d-glucopyranoside (1), (6Z)-3-hydroxymethyl-7-methylocta-1,6-dien-3-ol 8-O-beta-d-glucopyranoside (2), (6E)-3-hydroxymethyl-7-methylocta-1,6-dien-3-ol 8-O-beta-d-gluco-pyranoside (3), and 7-[(beta-d-apiofuranosyl-(1-->6)-beta-d-glucopyranosyl)oxymethy]-8,8-dimethyl-4,8 -dihydrobenzo[1,4]thiazine-3,5-dione (4), were isolated from the fruits of Xanthium sibiricum Patr together with three known compounds, Xanthiside (5), adenosine (6), and 2,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)-propan-1-one (7). The structures of the new compounds were determined on the basis of detailed spectroscopic analyses.

A new heterocyclic glucoside from the fruits of Xanthium pungens.[Pubmed:16010824]

Nat Prod Res. 2005 Sep;19(6):585-9.

A new thiazinedione glucoside, 7-(beta-D-glucopyranosyloxymethyl)-8,8-dimethyl-4,8-dihydrobenzo[1,4]thiazine-3,5 -dione (1) and named Xanthiside, was isolated from the methanol extract of the fruits of Xanthium pungens. Its structure was determined by spectroscopic techniques including, IR, CIMS, high-resolution-EIMS, and extensive 400 MHz one- and two-dimensional NMR-analysis (1H, 13C-NMR, DEPT, 1H-1H COSY, HMQC, COLOC, and NOE experiments).

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