Acanthoside BCAS# 7374-79-0 |
- Episyringaresinol 4'-O-β-D-glncopyranoside
Catalog No.:BCC8957
CAS No.:137038-13-2
- Tortoside A
Catalog No.:BCN9131
CAS No.:190655-16-4
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
| Cas No. | 7374-79-0 | SDF | Download SDF |
| PubChem ID | 443024 | Appearance | Powder |
| Formula | C28H36O13 | M.Wt | 580.6 |
| Type of Compound | Lignans | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | (2S,3R,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol | ||
| SMILES | COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC | ||
| Standard InChIKey | WEKCEGQSIIQPAQ-IRBNZIFYSA-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 | Acanthoside has inhibitory effects on the allergic inflammation. |
| Targets | Immunology & Inflammation related |
| In vitro | Inhibitory effects of chiisanoside and acanthoside on the allergic inflammation.[Reference: WebLink]Mol.Cell.Toxicol., 2007, 3(4):60-60.Inhibitory effects of chiisanoside and acanthoside on the allergic inflammation. |
| Structure Identification | Nat Prod Commun. 2013 Mar;8(3):333-4.Andrographidine G, a new flavone glucoside from Andrographis paniculata.[Pubmed: 23678804]A new flavone glucoside, andrographidine G (1), was isolated from Andrographis paniculata together with 13 known compounds, including flavonoids, diterpenoids, and iridoids.
Arch Pharm Res. 2011 Dec;34(12):2065-71.Multiple component quantitative analysis for the pattern recognition and quality evaluation of Kalopanacis Cortex using HPLC.[Pubmed: 22210032]A quantitative and pattern recognition analyses were conducted for quality evaluation of Kalopanacis Cortex (KC) using HPLC.
|
Acanthoside B Dilution Calculator
Acanthoside B Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 1.7224 mL | 8.6118 mL | 17.2236 mL | 34.4471 mL | 43.0589 mL |
| 5 mM | 0.3445 mL | 1.7224 mL | 3.4447 mL | 6.8894 mL | 8.6118 mL |
| 10 mM | 0.1722 mL | 0.8612 mL | 1.7224 mL | 3.4447 mL | 4.3059 mL |
| 50 mM | 0.0344 mL | 0.1722 mL | 0.3445 mL | 0.6889 mL | 0.8612 mL |
| 100 mM | 0.0172 mL | 0.0861 mL | 0.1722 mL | 0.3445 mL | 0.4306 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
- Broussonin A
Catalog No.:BCN4592
CAS No.:73731-87-0
- Broussonin B
Catalog No.:BCN4593
CAS No.:73731-86-9
- Fmoc-Thr-OH
Catalog No.:BCC3549
CAS No.:73731-37-0
- Fmoc-Ser-OH
Catalog No.:BCC3541
CAS No.:73724-45-5
- Acetylursolic acid
Catalog No.:BCN4290
CAS No.:7372-30-7
- Oxypeucedanin
Catalog No.:BCN2494
CAS No.:737-52-0
- Onysilin
Catalog No.:BCN3379
CAS No.:73695-94-0
- Naringenin 5-rhamnoside
Catalog No.:BCN2747
CAS No.:
- HEPES
Catalog No.:BCC7590
CAS No.:7365-45-9
- H-Asp-OBzl
Catalog No.:BCC2882
CAS No.:7362-93-8
- p-Coumaric acid ethyl ester
Catalog No.:BCN4289
CAS No.:7362-39-2
- 5-Amino-1-(2-hydroxyethyl)pyrazole
Catalog No.:BCC8727
CAS No.:73616-27-0
- N-(4-Aminobenzoyl)-β-alanine
Catalog No.:BCC9056
CAS No.:7377-08-4
- 360A iodide
Catalog No.:BCC1308
CAS No.:737763-37-0
- Kihadanin B
Catalog No.:BCN3441
CAS No.:73793-68-7
- Trimethoprim
Catalog No.:BCC4873
CAS No.:738-70-5
- Bergamotine
Catalog No.:BCN2733
CAS No.:7380-40-7
- S-Sulfo-L-cysteine sodium salt
Catalog No.:BCC6558
CAS No.:7381-67-1
- Orientin 2''-O-p-trans-coumarate
Catalog No.:BCN2792
CAS No.:73815-15-3
- 2,6-Dimethyl-7-octene-2,3,6-triol
Catalog No.:BCN4292
CAS No.:73815-21-1
- Boc-Asp(OcHex)-OH
Catalog No.:BCC3365
CAS No.:73821-95-1
- Boc-Glu(OcHex)-OH
Catalog No.:BCC3390
CAS No.:73821-97-3
- 3-Amino-9H-pyrido[3,4-b]indole
Catalog No.:BCC8617
CAS No.:73834-77-2
- Foresaconitine
Catalog No.:BCC8173
CAS No.:73870-35-6
Andrographidine G, a new flavone glucoside from Andrographis paniculata.[Pubmed:23678804]
Nat Prod Commun. 2013 Mar;8(3):333-4.
A new flavone glucoside, andrographidine G (1), was isolated from Andrographis paniculata together with 13 known compounds, including flavonoids, diterpenoids, and iridoids. The structure of 1 was established by spectroscopic and spectrometric techniques, including HR-ESI-TOF-MS, 1D and 2D NMR, and chemical methods. The known compounds were identified as andrographidine A (2), (2R)-5-hydroxy-7,8-dimethoxyflavanone-5-O-beta-D-glucopyranoside (3), Acanthoside B (4), neoandrographiside (5), andropanoside (6), andrographiside (7), andrographolide (8), 14-deoxy-11,12-didehydroandrographiside (9), 14-deoxy-11,12-didehydroandrographolide (10), procumbide (11), procumboside (12), 6-epi-8-O-acetylharpagide (13), and curvifloruside F (14).
Multiple component quantitative analysis for the pattern recognition and quality evaluation of Kalopanacis Cortex using HPLC.[Pubmed:22210032]
Arch Pharm Res. 2011 Dec;34(12):2065-71.
A quantitative and pattern recognition analyses were conducted for quality evaluation of Kalopanacis Cortex (KC) using HPLC. For quantitative analysis, four bioactive compounds, liriodendrin, pinoresinol O-beta-D-glucopyranoside, Acanthoside B and kalopanaxin B, were determined. The analysis method was optimized and validated using ODS column with mobile phase of methanol and aqueous phosphoric acid. The validation gave acceptable linearities (r > 0.9995), recoveries (98.4% to 101.9%) and precisions (RSD < 2.20). The limit of detection of compounds ranged from 0.4 to 0.9 mug/mL. Among the four compounds, liriodendrin was recommended as a marker compound for the quality control of KC. The pattern analysis was successfully carried out by analyzing thirty two samples from four species, and the authentic KC samples were completely discriminated from other inauthentic species by linear discriminant analysis. The results indicated that the method was suitable for the quantitative analysis of liriodendrin and the quality evaluation of KC.
