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Isosalvianolic acid C

CAS# 142115-17-1

Isosalvianolic acid C

Catalog No. BCN3476----Order now to get a substantial discount!

Product Name & Size Price Stock
Isosalvianolic acid C: 5mg Please Inquire In Stock
Isosalvianolic acid C: 10mg Please Inquire In Stock
Isosalvianolic acid C: 20mg Please Inquire Please Inquire
Isosalvianolic acid C: 50mg Please Inquire Please Inquire
Isosalvianolic acid C: 100mg Please Inquire Please Inquire
Isosalvianolic acid C: 200mg Please Inquire Please Inquire
Isosalvianolic acid C: 500mg Please Inquire Please Inquire
Isosalvianolic acid C: 1000mg Please Inquire Please Inquire

Quality Control of Isosalvianolic acid C

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Chemical structure

Isosalvianolic acid C

3D structure

Chemical Properties of Isosalvianolic acid C

Cas No. 142115-17-1 SDF Download SDF
PubChem ID 44566967 Appearance Powder
Formula C26H20O10 M.Wt 492.4
Type of Compound Phenylpropanoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (2R)-3-(3,4-dihydroxyphenyl)-2-[(E)-3-(2,3,10-trihydroxybenzo[b][1]benzoxepin-7-yl)prop-2-enoyl]oxypropanoic acid
SMILES C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C=CC4=CC(=C(C=C4OC3=C(C=C2)O)O)O)O)O
Standard InChIKey AVGRZVZQTALJJF-VURDRKPISA-N
Standard InChI InChI=1S/C26H20O10/c27-17-6-1-13(9-19(17)29)10-23(26(33)34)35-24(32)8-4-14-3-7-18(28)25-16(14)5-2-15-11-20(30)21(31)12-22(15)36-25/h1-9,11-12,23,27-31H,10H2,(H,33,34)/b8-4+/t23-/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 Isosalvianolic acid C

The herbs of Tournefortia sarmentosa.

Biological Activity of Isosalvianolic acid C

Description1. Isosalvianolic acid C exhibits more potent activity than probucol except for salvianolic acid F .
TargetsLDL

Isosalvianolic acid C Dilution Calculator

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Isosalvianolic acid C Molarity Calculator

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Preparing Stock Solutions of Isosalvianolic acid C

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.0309 mL 10.1543 mL 20.3087 mL 40.6174 mL 50.7717 mL
5 mM 0.4062 mL 2.0309 mL 4.0617 mL 8.1235 mL 10.1543 mL
10 mM 0.2031 mL 1.0154 mL 2.0309 mL 4.0617 mL 5.0772 mL
50 mM 0.0406 mL 0.2031 mL 0.4062 mL 0.8123 mL 1.0154 mL
100 mM 0.0203 mL 0.1015 mL 0.2031 mL 0.4062 mL 0.5077 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 Isosalvianolic acid C

Anti-lipid-peroxidative principles from Tournefortia sarmentosa.[Pubmed:12027757]

J Nat Prod. 2002 May;65(5):745-7.

Using the inhibition of Cu(2+)-induced low-density-lipoprotein (LDL) peroxidation to direct fractionation, four new benzenoids, tournefolal (1), tournefolic acids A (2) and B (3), and B ethyl ester (4), together with salvianolic acid A (5), Isosalvianolic acid C (6), lithospermic acid (7), salvianolic acid F (8), and rosmarinic acid (9), were isolated from the stems of Tournefortia sarmentosa. The structures of the new compounds 1-4 were elucidated on the basis of spectral and chemical methods. Furthermore, the anti-LDL-peroxidative activity of the isolated compounds was determined. All isolated compounds exhibited more potent activity than probucol except for salvianolic acid F (8).

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