6'-O-beta-D-ApiofuranosylswerosideCAS# 266678-59-5 |
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
| 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. |
||
| 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. | ||
| 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. | |||||
Calcutta University
University of Minnesota
University of Maryland School of Medicine
University of Illinois at Chicago
The Ohio State University
University of Zurich
Harvard University
Colorado State University
Auburn University
Yale University
Worcester Polytechnic Institute
Washington State University
Stanford University
University of Leipzig
Universidade da Beira Interior
The Institute of Cancer Research
Heidelberg University
University of Amsterdam
University of Auckland
TsingHua University
The University of Michigan
Miami University
DRURY University
Jilin University
Fudan University
Wuhan University
Sun Yat-sen University
Universite de Paris
Deemed University
Auckland University
The University of Tokyo
Korea University
- N4-Benzoylcytosine
Catalog No.:BCC9073
CAS No.:26661-13-2
- Dipalmitin
Catalog No.:BCN2214
CAS No.:26657-95-4
- Salirepin
Catalog No.:BCN5149
CAS No.:26652-12-0
- Conodurine
Catalog No.:BCN7463
CAS No.:2665-57-8
- Reparixin L-lysine salt
Catalog No.:BCC1886
CAS No.:266359-93-7
- Reparixin
Catalog No.:BCC1885
CAS No.:266359-83-5
- Fmoc-β-Homo-Met-OH
Catalog No.:BCC2630
CAS No.:266359-48-2
- Zotepine
Catalog No.:BCC7838
CAS No.:26615-21-4
- 3-Ethoxyandrosta-3,5-dien-17β-ol
Catalog No.:BCC8631
CAS No.:26614-48-2
- Z-D-Ala-OH
Catalog No.:BCC3059
CAS No.:26607-51-2
- SCH 202676 hydrobromide
Catalog No.:BCC7049
CAS No.:265980-25-4
- Crenatine
Catalog No.:BCN5148
CAS No.:26585-14-8
- Boc-Glycinol
Catalog No.:BCC3093
CAS No.:26690-80-2
- Picraline
Catalog No.:BCN4762
CAS No.:2671-32-1
- [Nphe1]Nociceptin(1-13)NH2
Catalog No.:BCC5739
CAS No.:267234-08-2
- Canertinib
Catalog No.:BCN2172
CAS No.:267243-28-7
- Perivine
Catalog No.:BCN2583
CAS No.:2673-40-7
- Alibendol
Catalog No.:BCC4758
CAS No.:26750-81-2
- Amoxicillin
Catalog No.:BCC4625
CAS No.:26787-78-0
- Robtein
Catalog No.:BCN4658
CAS No.:2679-65-4
- Xanthatin
Catalog No.:BCN5150
CAS No.:26791-73-1
- Dehydrodiisoeugenol
Catalog No.:BCN1240
CAS No.:2680-81-1
- Indapamide
Catalog No.:BCC4788
CAS No.:26807-65-8
- Debilon
Catalog No.:BCN7696
CAS No.:26808-51-5
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.
