Purpureaside CCAS# 108648-07-3 |
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| Cas No. | 108648-07-3 | SDF | Download SDF |
| PubChem ID | 11953944 | Appearance | Powder |
| Formula | C35H46O20 | M.Wt | 786.7 |
| Type of Compound | Phenylpropanoids | Storage | Desiccate at -20°C |
| Solubility | DMSO : 125 mg/mL (158.89 mM; Need ultrasonic) | ||
| Chemical Name | [(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-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)COC4C(C(C(C(O4)CO)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O | ||
| Standard InChIKey | FSBUXLDOLNLABB-HSCIEKESSA-N | ||
| Standard InChI | InChI=1S/C35H46O20/c1-14-24(42)26(44)29(47)35(51-14)55-32-30(48)34(49-9-8-16-3-6-18(38)20(40)11-16)53-22(13-50-33-28(46)27(45)25(43)21(12-36)52-33)31(32)54-23(41)7-4-15-2-5-17(37)19(39)10-15/h2-7,10-11,14,21-22,24-40,42-48H,8-9,12-13H2,1H3/b7-4+/t14-,21+,22+,24-,25-,26+,27-,28+,29+,30+,31+,32+,33+,34+,35-/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 roots of Rehmannia glutinosa
| Description | 1. Purpureaside C has significant proinflammatory, antimicrobial and immunomodulating effects. |
| Targets | Immunology & Inflammation related | Antifection |
Purpureaside C Dilution Calculator
Purpureaside C Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 1.2711 mL | 6.3557 mL | 12.7113 mL | 25.4227 mL | 31.7783 mL |
| 5 mM | 0.2542 mL | 1.2711 mL | 2.5423 mL | 5.0845 mL | 6.3557 mL |
| 10 mM | 0.1271 mL | 0.6356 mL | 1.2711 mL | 2.5423 mL | 3.1778 mL |
| 50 mM | 0.0254 mL | 0.1271 mL | 0.2542 mL | 0.5085 mL | 0.6356 mL |
| 100 mM | 0.0127 mL | 0.0636 mL | 0.1271 mL | 0.2542 mL | 0.3178 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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Antimicrobial and immunomodulating effects of some phenolic glycosides.[Pubmed:2701348]
Acta Microbiol Hung. 1989;36(4):425-32.
Several phenolic glycosides, i.e. acteoside, desrhamnosyl acteoside, and purpureaside A, B and C, exerted weak antibacterial effects on Escherichia coli. Acteoside had antiplasmid effects, including F'lac plasmid elimination, and inhibited kanamycin resistance transfer in E. coli. Acteoside, desrhamnosyl acteoside and purpureaside A displayed antiviral effect on Aujeszky virus. All of the phenolic glycosides decreased some human leucocyte functions, including rosette formation, mitogen-induced blast transformation and phagocytic activity in vitro. The Purpureaside C had significant proinflammatory action, however, other phenolic glycosides showed neither proinflammatory nor antiinflammatory effect on carrageenin-induced inflammation in vivo.
Purpureaside C is a phenolic glycoside and has significant proinflammatory action.
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