ConicaosideCAS# 916888-05-6 |
Quality Control & MSDS
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Number of papers citing our products
| Cas No. | 916888-05-6 | SDF | Download SDF |
| PubChem ID | N/A | Appearance | Powder |
| Formula | C27H36O12 | M.Wt | 552.63 |
| Type of Compound | Lignans | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| 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. | ||
Conicaoside Dilution Calculator
Conicaoside Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 1.8095 mL | 9.0476 mL | 18.0953 mL | 36.1906 mL | 45.2382 mL |
| 5 mM | 0.3619 mL | 1.8095 mL | 3.6191 mL | 7.2381 mL | 9.0476 mL |
| 10 mM | 0.181 mL | 0.9048 mL | 1.8095 mL | 3.6191 mL | 4.5238 mL |
| 50 mM | 0.0362 mL | 0.181 mL | 0.3619 mL | 0.7238 mL | 0.9048 mL |
| 100 mM | 0.0181 mL | 0.0905 mL | 0.181 mL | 0.3619 mL | 0.4524 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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[Lignans from flower buds of Magnolia biondii].[Pubmed:29676096]
Zhongguo Zhong Yao Za Zhi. 2018 Mar;43(5):970-976.
The present study aims to investigate the lignans from the flower buds of Magnolia biondii. The isolation and purification of the compounds were performed by column chromatographies on Diaion HP-20, silica gel, and Sephadex LH-20, combined with semi-preparative HPLC. Their structures were elucidated on the basis of spectral data and physiochemical properties. Eighteen compounds were isolated and identified as magnolin (1), epimagnolin (2), eudesmin (3), kobusin (4), aschantin (5), lirioresinol B dimethyl ether (6), pinoresinol monomethy ether (7), (+)-de-O-methylmagnolin (8), isoeucommin A (9), syringaresinol 4-O-beta-D-glucopyranoside (10), phillygenin (11), lariciresinol-4'-O-beta-1-D-glucoside (12), Conicaoside (13), (7'S, 8'R)-dihydrodehydrodiconiferylalcohol (14), 7R*, 8S*-dihydrodehydrodiconiferyl alcohol 4-O-beta-D-glucopyranoside (15), 7S, 8R-erythro-7, 9, 9'-trihydroxy-3, 3'-dimethoxy-8-O-4'-neolignan 4-O-beta-D-glucopyranoside (16), 7S, 8R-erythro-4, 9, 9'-trihydroxy-3, 3'-dimethoxy-8-O-4'-neolignan-7-O-beta-D-glucopyranoside (17), and (+)-isolariciresinol (18). Compounds 7-18 are isolated from this plant for the first time.
[Lignans from stems of Cistanche deserticola cultured in Tarim desert].[Pubmed:26084171]
Zhongguo Zhong Yao Za Zhi. 2015 Feb;40(3):463-8.
In order to clarify the chemical constituents of Cistanche deserticola cultured in Tarim desert, a systematically phytochemical investigation was carried out. The chemical constituents were isolated by column chromatography, such as silica gel, Sephadex LH- 20, MCI gel, ODS and semi-preparative HPLC, and their structures were determined on the basis of MS, NMR spectroscopic analysis and/or comparison with literature data. Eleven lignans were isolated from the 85% ethanol extract of the stems of C. deserticola cultured in Tarim desert. Their structures were identified as (+)-syringaresinol-4'-O-beta-D-glucopyranoside (1), (+)-isoeucommin A (2), eucommin A (3), (+)-pinoresinol monomethylether beta-D-glucoside (4), lariciresinol 4'-O-beta-D-glucopyranoside (5), lariciresinol 4-O-beta-D-glucopyranoside (6), Conicaoside (7), dehydrodiconiferyl alcohol 4-O-beta-D-glucopyranoside (8), dehydrodiconiferyl alcohol gamma'-O-beta-D-glucoside (9), citrusin A (10), and alaschanioside A (11). Compounds 1, 3-7, 10 and 11 were isolated from this genus for the first time, and compounds 2, 8 and 9 were obtained from this species for the first time.
Lignans from Saussurea conica and their NO production suppressing activity.[Pubmed:16636966]
Planta Med. 2006 Jun;72(7):590-5.
Three new lignan derivatives, conicaols A and B and Conicaoside, together with seven known compounds were identified from Saussurea conica. Their structures were elucidated by spectral methods including 1D and 2D NMR techniques. Six 2,3-dibenzylbutyrolactone-type lignans were biologically evaluated, and two of them, arctigenin and matairesinol, showed potent activity to suppress NO production in vitro in LPS-activated macrophages of SD rat.
