6'-O-beta-D-ApiofuranosylswerosideCAS# 266678-59-5 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 266678-59-5 | SDF | Download SDF |
| PubChem ID | 10696407 | Appearance | Powder |
| Formula | C21H30O13 | M.Wt | 490.5 |
| Type of Compound | Iridoids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | (3S,4R,4aS)-3-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-ethenyl-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one | ||
| SMILES | C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O | ||
| Standard InChIKey | JNPXCTROEJQHKD-APAPHXOESA-N | ||
| 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 | 6'-O-beta-D-Apiofuranosylsweroside is a natural product from Lonicera maackii. |
| Structure Identification | Drugs & Clinic ,2014, 29 (5) :459-464.Chemical constituents of Dipsaci Radix.[Reference: WebLink]To study the chemical constituents of Dipsaci Radix. Methods The compounds were isolated by macroporous resin, reverse phase C18 silica gel, and semi-prepative HPLC. Their structures were identified on the basis of physicochemical properties and spectroscopic data. Results Thirteen compounds were separated, seven of which were iridoid glycosides, and six of which were lignans, identified as loganin(1), sweroside(2), 6'-O-beta-D-Apiofuranosylsweroside(3), dipsanoside H(4), dipsanoside F(5), dipsanoside E(6), triplostoside A(7),(7R, 8S, 7'R, 8'S)-5-methoxyprinsepiol-4-O-β-D-glucopyranoside(8),(7R, 8S, 7'R, 8'S)-prinsepiol-4-O-β-D-glucopyranoside(9), acanthoside D(10),(7R, 8S, 7'R, 8'S)-fraxiresinol-4'-O-β-D-glucopyranoside(11),(7R, 8S, 7'R, 8'S)-8-hydroxypinoresinol-4'-O-β-D-glucopyranoside(12), and(7R, 8S, 7'R, 8'S)-8-hydroxypinoresinol-4-O-β-Dglucopyranoside(13), respectively. Conclusion Compounds 8, 9, and 11—13 are isolated from this genus for the first time. |
6'-O-beta-D-Apiofuranosylsweroside Dilution Calculator
6'-O-beta-D-Apiofuranosylsweroside Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 2.0387 mL | 10.1937 mL | 20.3874 mL | 40.7747 mL | 50.9684 mL |
| 5 mM | 0.4077 mL | 2.0387 mL | 4.0775 mL | 8.1549 mL | 10.1937 mL |
| 10 mM | 0.2039 mL | 1.0194 mL | 2.0387 mL | 4.0775 mL | 5.0968 mL |
| 50 mM | 0.0408 mL | 0.2039 mL | 0.4077 mL | 0.8155 mL | 1.0194 mL |
| 100 mM | 0.0204 mL | 0.1019 mL | 0.2039 mL | 0.4077 mL | 0.5097 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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Chemical constituents of Dipsaci Radix.
Drugs & Clinic ,2014, 29 (5) :459-464.
To study the chemical constituents of Dipsaci Radix. Methods The compounds were isolated by macroporous resin, reverse phase C18 silica gel, and semi-prepative HPLC. Their structures were identified on the basis of physicochemical properties and spectroscopic data. Results Thirteen compounds were separated, seven of which were iridoid glycosides, and six of which were lignans, identified as loganin(1), sweroside(2), 6'-O-beta-D-Apiofuranosylsweroside(3), dipsanoside H(4), dipsanoside F(5), dipsanoside E(6), triplostoside A(7),(7R, 8S, 7'R, 8'S)-5-methoxyprinsepiol-4-O-β-D-glucopyranoside(8),(7R, 8S, 7'R, 8'S)-prinsepiol-4-O-β-D-glucopyranoside(9), acanthoside D(10),(7R, 8S, 7'R, 8'S)-fraxiresinol-4'-O-β-D-glucopyranoside(11),(7R, 8S, 7'R, 8'S)-8-hydroxypinoresinol-4'-O-β-D-glucopyranoside(12), and(7R, 8S, 7'R, 8'S)-8-hydroxypinoresinol-4-O-β-Dglucopyranoside(13), respectively. Conclusion Compounds 8, 9, and 11—13 are isolated from this genus for the first time.
