Junipediol ACAS# 86548-91-6 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 86548-91-6 | SDF | Download SDF |
| PubChem ID | 86072622 | Appearance | Powder |
| Formula | C10H14O4 | M.Wt | 198.22 |
| Type of Compound | Phenylpropanoids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | 2-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol | ||
| SMILES | COC1=C(C=CC(=C1)C(CO)CO)O | ||
| Standard InChIKey | UIDMTMWJXFPCFC-UHFFFAOYSA-N | ||
| Standard InChI | InChI=1S/C10H14O4/c1-14-10-4-7(2-3-9(10)13)8(5-11)6-12/h2-4,8,11-13H,5-6H2,1H3 | ||
| 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. |
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| 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. |
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| 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. | ||
| Description | 1. Junipediol A shows antioxidation activity. |
Junipediol A Dilution Calculator
Junipediol A Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 5.0449 mL | 25.2245 mL | 50.449 mL | 100.898 mL | 126.1225 mL |
| 5 mM | 1.009 mL | 5.0449 mL | 10.0898 mL | 20.1796 mL | 25.2245 mL |
| 10 mM | 0.5045 mL | 2.5224 mL | 5.0449 mL | 10.0898 mL | 12.6122 mL |
| 50 mM | 0.1009 mL | 0.5045 mL | 1.009 mL | 2.018 mL | 2.5224 mL |
| 100 mM | 0.0504 mL | 0.2522 mL | 0.5045 mL | 1.009 mL | 1.2612 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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Water-soluble constituents of caraway: aromatic compound, aromatic compound glucoside and glucides.[Pubmed:12377243]
Phytochemistry. 2002 Oct;61(4):455-9.
From the water-soluble portion of the methanolic extract of caraway (fruit of Carum carvi L.), an aromatic compound, an aromatic compound glucoside and a glucide were isolated together with 16 known compounds. Their structures were clarified as 2-methoxy-2-(4'-hydroxyphenyl)ethanol, Junipediol A 2-O-beta-D-glucopyranoside and L-fucitol, respectively.
Identification of a new angiotensin-converting enzyme (ACE) inhibitor from Thai edible plants.[Pubmed:25038653]
Food Chem. 2014 Dec 15;165:92-7.
Eight Thai edible plants were tested for their inhibitory activity against an angiotensin-converting enzyme (ACE) using an in vitro assay. The methanol extract of Apium graveolens exhibited significant ACE inhibitory activity with an IC50 value of 1.7 mg/ml, and was then subjected to an isolation procedure that resulted in identification of a pure active constituent, Junipediol A 8-O-beta-d-glucoside (1-beta-d-glucosyloxy-2-(3-methoxy-4-hydroxyphenyl)-propane-1,3-diol) (1), which had good ACE inhibitory activity with an IC50 value of 76 mug/ml. Another eight known compounds, isofraxidin-beta-d-glucoside (2), roseoside (3), apigenin-7-O-beta-d-glucoside (4), luteolin-7-O-beta-d-glucoside (5), icariside D2 (6), apiin (7), chrysoeriol-7-O-beta-d-apiosylglucoside (8), and 11,21-dioxo-3 beta,15 alpha,24-trihydroxyurs-12-ene-24-O-beta-d-glucopyranoside (9) were also identified. Although each of these five constituents (2-6) isolated from the same fraction as 1 showed no activity at concentrations of 500 muM, together, when each was present at 300 mug/ml, they enhanced the inhibitory activity of 500 muM of 1 from 64% to 81%.
