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6-O-(3'',4''-Dimethoxycinnamoyl)catalpol

CAS# 147714-71-4

6-O-(3'',4''-Dimethoxycinnamoyl)catalpol

Catalog No. BCN1655----Order now to get a substantial discount!

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Quality Control of 6-O-(3'',4''-Dimethoxycinnamoyl)catalpol

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Chemical structure

6-O-(3'',4''-Dimethoxycinnamoyl)catalpol

3D structure

Chemical Properties of 6-O-(3'',4''-Dimethoxycinnamoyl)catalpol

Cas No. 147714-71-4 SDF Download SDF
PubChem ID 91895357 Appearance Powder
Formula C26H32O13 M.Wt 552.5
Type of Compound Iridoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name [(1S,2S,4S,5S,6R,10S)-2-(hydroxymethyl)-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-5-yl] (E)-3-(3,4-dimethoxyphenyl)prop-2-enoate
SMILES COC1=C(C=C(C=C1)C=CC(=O)OC2C3C=COC(C3C4(C2O4)CO)OC5C(C(C(C(O5)CO)O)O)O)OC
Standard InChIKey UGUWZDBHHDVSKD-JFBQKNIMSA-N
Standard InChI InChI=1S/C26H32O13/c1-33-14-5-3-12(9-15(14)34-2)4-6-17(29)37-22-13-7-8-35-24(18(13)26(11-28)23(22)39-26)38-25-21(32)20(31)19(30)16(10-27)36-25/h3-9,13,16,18-25,27-28,30-32H,10-11H2,1-2H3/b6-4+/t13-,16-,18-,19-,20+,21-,22+,23+,24+,25+,26-/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 6-O-(3'',4''-Dimethoxycinnamoyl)catalpol

The herbs of Buddleja asiatica Lour

Biological Activity of 6-O-(3'',4''-Dimethoxycinnamoyl)catalpol

Description1. 6-O-(3'',4''-Dimethoxycinnamoyl)catalpol has anti-hepatotoxic activity.

6-O-(3'',4''-Dimethoxycinnamoyl)catalpol Dilution Calculator

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6-O-(3'',4''-Dimethoxycinnamoyl)catalpol Molarity Calculator

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Preparing Stock Solutions of 6-O-(3'',4''-Dimethoxycinnamoyl)catalpol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.81 mL 9.0498 mL 18.0995 mL 36.1991 mL 45.2489 mL
5 mM 0.362 mL 1.81 mL 3.6199 mL 7.2398 mL 9.0498 mL
10 mM 0.181 mL 0.905 mL 1.81 mL 3.6199 mL 4.5249 mL
50 mM 0.0362 mL 0.181 mL 0.362 mL 0.724 mL 0.905 mL
100 mM 0.0181 mL 0.0905 mL 0.181 mL 0.362 mL 0.4525 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 6-O-(3'',4''-Dimethoxycinnamoyl)catalpol

Antihepatotoxic activity and chemical constituents of Buddleja asiatica Lour.[Pubmed:19323260]

Z Naturforsch C. 2009 Jan-Feb;64(1-2):11-9.

A new natural compound, named 6-O-(3",4"-dimethoxycinnamoyl) catalpol, was isolated from the defatted alcoholic extract of the flowering parts of Buddleja asiatica Lour. (family Scrophulariaceae). Other separated known compounds included steroids (beta-sitosterol, stigmasterol, stigmasterol-O-glucoside, beta-sitosterol-O-glucoside), iridoid glucosides (methyl catalpol, catalpol, aucubin), phenylpropanoids (isoacteoside and acteoside), a triterpene saponin (mimengoside A), flavonoids (diosmin and linarin) in addition to the free sugars mannitol and sucrose. The structures of the isolated compounds were established by 1H and 13C NMR and mass spectrometry. Furthermore, the polar fraction of the flowering parts and the roots showed substantial antihepatotoxic activity comparable to that of the lignan silymarin.

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