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3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid

CAS# 477873-63-5

3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid

Catalog No. BCN7068----Order now to get a substantial discount!

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3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid: 5mg $828 In Stock
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Quality Control of 3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid

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Chemical structure

3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid

3D structure

Chemical Properties of 3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid

Cas No. 477873-63-5 SDF Download SDF
PubChem ID 11100427 Appearance Powder
Formula C16H22O9 M.Wt 358.34
Type of Compound Phenylpropanoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 3-[4-methoxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoic acid
SMILES COC1=CC(=C(C=C1)CCC(=O)O)OC2C(C(C(C(O2)CO)O)O)O
Standard InChIKey LIVNOUBJFOXZOR-YMILTQATSA-N
Standard InChI InChI=1S/C16H22O9/c1-23-9-4-2-8(3-5-12(18)19)10(6-9)24-16-15(22)14(21)13(20)11(7-17)25-16/h2,4,6,11,13-17,20-22H,3,5,7H2,1H3,(H,18,19)/t11-,13-,14+,15-,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 3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid

The barks of Caesalpinia bonduc.

Biological Activity of 3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid

Description1. 2-O-beta-d-Glucosyloxy-4-methoxybenzenepropanoic acid[3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid] exhibits glutathione S-transferase (GST) inhibitory and antifungal activities.
TargetsAntifection

3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid Dilution Calculator

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3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid Molarity Calculator

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Preparing Stock Solutions of 3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.7906 mL 13.9532 mL 27.9065 mL 55.8129 mL 69.7661 mL
5 mM 0.5581 mL 2.7906 mL 5.5813 mL 11.1626 mL 13.9532 mL
10 mM 0.2791 mL 1.3953 mL 2.7906 mL 5.5813 mL 6.9766 mL
50 mM 0.0558 mL 0.2791 mL 0.5581 mL 1.1163 mL 1.3953 mL
100 mM 0.0279 mL 0.1395 mL 0.2791 mL 0.5581 mL 0.6977 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 3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid

Bioactive chemical constituents of Caesalpinia bonduc (Fabaceae).

Phytochemistry Letters, 2009, 2(3):106-109.

Phytochemical studies on the ethanolic extracts of Caesalpinia bonduc (Fabaceae) yielded two new homoisoflavonoids, caesalpinianone, and 6-O-methylcaesalpinianone along with five known natural products, namely, hematoxylol, stereochenol A, 6′-O-acetylloganic acid, 4′-O-acetylloganic acid, and 2-O-β-d-glucosyloxy-4-methoxybenzenepropanoic acid[3-(2-Glucosyloxy-4-methoxyphenyl)propanoic acid]. Structures of these compounds were elucidated with the aid of extensive NMR spectral studies. All of these compounds exhibited different levels of glutathione S-transferase (GST) inhibitory and antifungal activities.

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