BrachynosideCAS# 145898-87-9 |
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| Cas No. | 145898-87-9 | SDF | Download SDF |
| PubChem ID | 10032232 | Appearance | Powder |
| Formula | C31H40O15 | M.Wt | 652.7 |
| Type of Compound | Phenylpropanoids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | [(2R,3R,4R,5R,6R)-6-[2-(3,4-dimethoxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate | ||
| SMILES | CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)OC)OC)O)O)O)O | ||
| Standard InChIKey | XFXLUFBHZDVJDO-CNMJWYMJSA-N | ||
| Standard InChI | InChI=1S/C31H40O15/c1-15-24(36)25(37)26(38)31(43-15)46-29-27(39)30(42-11-10-17-5-8-20(40-2)21(13-17)41-3)44-22(14-32)28(29)45-23(35)9-6-16-4-7-18(33)19(34)12-16/h4-9,12-13,15,22,24-34,36-39H,10-11,14H2,1-3H3/b9-6+/t15-,22+,24-,25+,26+,27+,28+,29+,30+,31-/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. |
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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. | ||
The herbs of Clerodendrum japonicum
| Description | Brachynoside is a natural product from Clerodendrum japonicum. |
| Structure Identification | Chemical & Pharmaceutical Bulletin , 1992 , 40 (7) :1928-1929.A New Glycoside, Brachynoside, Isolated from Clerodendron brachyanthum SCHAUER.[Reference: WebLink]Eudesmin, syringaresinol dimethyl ether, kusaginin and Brachynoside were isolated from the ethanol extract of the leaves of Clerodendron brachyanthum. The new glycoside, branchynoside, was assigned as 2-(3, 4-dimethoxyphenyl)ethyl 3-O-α-L-rhamnopyranosyl-4-O-(3, 4-dihydroxycinnamoyl)-β-D-glucopyranoside from studies on partial methylation and methanolysis products and from analysis of spectroscopic evidence. |
Brachynoside Dilution Calculator
Brachynoside Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 1.5321 mL | 7.6605 mL | 15.321 mL | 30.6419 mL | 38.3024 mL |
| 5 mM | 0.3064 mL | 1.5321 mL | 3.0642 mL | 6.1284 mL | 7.6605 mL |
| 10 mM | 0.1532 mL | 0.766 mL | 1.5321 mL | 3.0642 mL | 3.8302 mL |
| 50 mM | 0.0306 mL | 0.1532 mL | 0.3064 mL | 0.6128 mL | 0.766 mL |
| 100 mM | 0.0153 mL | 0.0766 mL | 0.1532 mL | 0.3064 mL | 0.383 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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A New Glycoside, Brachynoside, Isolated from Clerodendron brachyanthum SCHAUER.
Chemical & Pharmaceutical Bulletin , 1992 , 40 (7) :1928-1929.
Eudesmin, syringaresinol dimethyl ether, kusaginin and Brachynoside were isolated from the ethanol extract of the leaves of Clerodendron brachyanthum. The new glycoside, branchynoside, was assigned as 2-(3, 4-dimethoxyphenyl)ethyl 3-O-α-L-rhamnopyranosyl-4-O-(3, 4-dihydroxycinnamoyl)-β-D-glucopyranoside from studies on partial methylation and methanolysis products and from analysis of spectroscopic evidence.
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