5'-MethoxylariciresinolCAS# 105256-12-0 |
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
| Cas No. | 105256-12-0 | SDF | Download SDF |
| PubChem ID | 184458 | Appearance | Powder |
| Formula | C21H26O7 | M.Wt | 390.43 |
| Type of Compound | Lignans | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | 4-[(2S,3R,4R)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-(hydroxymethyl)oxolan-2-yl]-2,6-dimethoxyphenol | ||
| SMILES | COC1=CC(=CC(=C1O)OC)C2C(C(CO2)CC3=CC(=C(C=C3)O)OC)CO | ||
| Standard InChIKey | CRMXIJILTLLGMR-VFCRVFHLSA-N | ||
| Standard InChI | InChI=1S/C21H26O7/c1-25-17-7-12(4-5-16(17)23)6-14-11-28-21(15(14)10-22)13-8-18(26-2)20(24)19(9-13)27-3/h4-5,7-9,14-15,21-24H,6,10-11H2,1-3H3/t14-,15-,21+/m0/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. | ||
| Description | 5'-Methoxylariciresinol is a natural product from Stellera chamaejasme. |
| Structure Identification | Zhongguo Zhong Yao Za Zhi. 2011 Dec;36(24):3457-62.Studies on chemical constitutes from callus cultures of Stellera chamaejasme.[Pubmed: 22368856]
Zhongguo Zhong Yao Za Zhi. 2012 May;37(9):1241-4.Non-alkaloid chemical constituents from Coptis chinensis.[Pubmed: 22803368]To separate and identify chemical constituents from Coptis chinensis. |
5'-Methoxylariciresinol Dilution Calculator
5'-Methoxylariciresinol Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 2.5613 mL | 12.8064 mL | 25.6128 mL | 51.2256 mL | 64.032 mL |
| 5 mM | 0.5123 mL | 2.5613 mL | 5.1226 mL | 10.2451 mL | 12.8064 mL |
| 10 mM | 0.2561 mL | 1.2806 mL | 2.5613 mL | 5.1226 mL | 6.4032 mL |
| 50 mM | 0.0512 mL | 0.2561 mL | 0.5123 mL | 1.0245 mL | 1.2806 mL |
| 100 mM | 0.0256 mL | 0.1281 mL | 0.2561 mL | 0.5123 mL | 0.6403 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
- SBE 13 HCl
Catalog No.:BCC6408
CAS No.:1052532-15-6
- Virosine B
Catalog No.:BCN6742
CAS No.:1052228-70-2
- WEB 2086
Catalog No.:BCC7335
CAS No.:105219-56-5
- PSB 06126
Catalog No.:BCC7417
CAS No.:1052089-16-3
- PSB 0739
Catalog No.:BCC6095
CAS No.:1052087-90-7
- Q94 hydrochloride
Catalog No.:BCC6281
CAS No.:1052076-77-3
- 9-Oxoageraphorone
Catalog No.:BCN5866
CAS No.:105181-06-4
- AC 264613
Catalog No.:BCC3952
CAS No.:1051487-82-1
- GSK1349572 sodiuM salt
Catalog No.:BCC6407
CAS No.:1051375-19-9
- S/GSK1349572
Catalog No.:BCC2138
CAS No.:1051375-16-6
- GSK744 (S/GSK1265744)
Catalog No.:BCC3888
CAS No.:1051375-10-0
- Ligucyperonol
Catalog No.:BCN6638
CAS No.:105108-20-1
- 3'-Deoxy-4-O-methylepisappanol
Catalog No.:BCN3676
CAS No.:1052714-12-1
- Ganodermatriol
Catalog No.:BCC8177
CAS No.:105300-28-5
- Aloeresin D
Catalog No.:BCN2850
CAS No.:105317-67-7
- Neocaesalpin O
Catalog No.:BCN7266
CAS No.:1053189-53-9
- 5,7,4'-Tri-O-methylcatechin
Catalog No.:BCN3951
CAS No.:105330-59-4
- Tanshinlactone
Catalog No.:BCN5867
CAS No.:105351-70-0
- Tyrphostin 9
Catalog No.:BCC4471
CAS No.:10537-47-0
- Shuterin
Catalog No.:BCN8068
CAS No.:105377-77-3
- Bis(3-ethyl-5-methyl-4-maleimidophenyl)methane
Catalog No.:BCC8881
CAS No.:105391-33-1
- Spiroxatrine
Catalog No.:BCC6728
CAS No.:1054-88-2
- Tamoxifen
Catalog No.:BCN1634
CAS No.:10540-29-1
- 7-Epitaxol
Catalog No.:BCN2514
CAS No.:105454-04-4
[Non-alkaloid chemical constituents from Coptis chinensis].[Pubmed:22803368]
Zhongguo Zhong Yao Za Zhi. 2012 May;37(9):1241-4.
OBJECTIVE: To separate and identify chemical constituents from Coptis chinensis. METHOD: The compounds were separated and purified by various chromatographic techniques. Their structures were identified on the basis of their physicochemical properties using spectral techniques such as NMR and MS. RESULT: Thirteen compounds were separated from ethanol extracts of C. chinensis, including seven lignans, three simple phenylpropanoids, two flavones and one phenolic acid, and identified as erythro-guaiacylglycerol-8-O-4'-(coniferyl alcohol) ether (1), threo-guaiacylglycerol-8-O-4'-(coniferyl alcohol) ether (2), (+)-pinoresinol (3), (+)-medioresinol (4), (+)-lariciresinol (5), (+)-5'-methoxylariciresinol (6), (+)-isolariciresinol (7), chlorogenic acid (8), ferulic acid (9), Z-octadecyl caffeate (10), rhamnetin (11), wogonin (12), and vanillic acid (13). CONCLUSION: Compounds 1, 2, 4, 6, 10-13 were separated from the genus Coptis for the first time.
[Studies on chemical constitutes from callus cultures of Stellera chamaejasme].[Pubmed:22368856]
Zhongguo Zhong Yao Za Zhi. 2011 Dec;36(24):3457-62.
From callus cultures of Stellera chamaejasme, 17 compounds were isolated. Based on their physical and chemical data and spectroscopic analysis, they were identified as syringaresinol (1), medioresinol (2), pinoresinol (3), (1R, 2S, 5R, 6S)- 2-(4- hydroxyphenyl)-6-(3-methoxy-4-hydroxyphenyl)-3, 7-dioxabicyclo [3, 3, 0] octane (4), epipinoresinol (5), caruilignan D (6), 3-oxo-guai-4-ene-11, 12-diol (7), (-) -lariciresinol (8), tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-[(4-hydroxyphenyl) methyl]-3-furanmethanol (9), 5'-methoxylariciresinol (10), vladinol D (11), cyclo (L-Pro-L-Val) (12), oxomatairesinol (13), (+) -guayarol (14); acutissimalignan B (15), isolariciresinol (16), and beta-sitosterol (17), respectively. Among these compounds, 12 was a cyclodipeptide, 7 was a sesquiterpene, and the others except 17 were lignans. All compounds were first isolated from callus cultures of S. chamaejasme.
