Fulvotomentoside ACAS# 150107-44-1 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 150107-44-1 | SDF | Download SDF |
| PubChem ID | 100998349.0 | Appearance | Powder |
| Formula | C58H94O26 | M.Wt | 1207.36 |
| Type of Compound | Triterpenoids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate | ||
| SMILES | CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)C)O)O)O)OC1C(C(C(CO1)O)O)O)O | ||
| Standard InChIKey | DQDTUCJCIHGIOL-XSGUKHGCSA-N | ||
| Standard InChI | InChI=1S/C58H94O26/c1-24-34(63)45(82-48-41(70)35(64)27(61)20-75-48)44(73)50(78-24)83-46-36(65)28(62)21-76-51(46)81-33-11-12-54(4)31(55(33,5)23-60)10-13-57(7)32(54)9-8-25-26-18-53(2,3)14-16-58(26,17-15-56(25,57)6)52(74)84-49-43(72)40(69)38(67)30(80-49)22-77-47-42(71)39(68)37(66)29(19-59)79-47/h8,24,26-51,59-73H,9-23H2,1-7H3/t24-,26-,27+,28-,29+,30+,31+,32+,33-,34-,35-,36-,37+,38+,39-,40-,41+,42+,43+,44+,45+,46+,47+,48-,49-,50-,51-,54-,55-,56+,57+,58-/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. | ||
Fulvotomentoside A Dilution Calculator
Fulvotomentoside A Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 0.8283 mL | 4.1413 mL | 8.2825 mL | 16.5651 mL | 20.7063 mL |
| 5 mM | 0.1657 mL | 0.8283 mL | 1.6565 mL | 3.313 mL | 4.1413 mL |
| 10 mM | 0.0828 mL | 0.4141 mL | 0.8283 mL | 1.6565 mL | 2.0706 mL |
| 50 mM | 0.0166 mL | 0.0828 mL | 0.1657 mL | 0.3313 mL | 0.4141 mL |
| 100 mM | 0.0083 mL | 0.0414 mL | 0.0828 mL | 0.1657 mL | 0.2071 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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[Protective effect of the fulvotomentosides on paracetamol-induced hepatotoxicity in mice].[Pubmed:7660799]
Yao Xue Xue Bao. 1995;30(4):311-4.
Fulvotomentoside Alpha-hederin (H) and sapindoside B (S) are two components of the fulvotomentosides reported to decrease the toxicity of a number of hepatotoxins in mice. We studied the effects of the mixture of alpha-hederin and sapindoside B (HS) on paracetamol (Par)-induced liver injury. HS (20 mg.kg-1 sc twice) was shown to decrease the mortality produced by Par. The liver injury produced by Par was remarkably decreased as indicated by decrease of sGPT and by histopathological examination. Additionally, HS mitigated the hepatic GSH depletion caused by Par. Par excretion into urine was increased following HS.
[Studies on the chemical constituents of Lonicera fulvotomentosa Hsu et S.C. Cheng].[Pubmed:2816388]
Yao Xue Xue Bao. 1989;24(4):269-74.
Five saponins (I-V) have been isolated from the flowers of Lonicera fulvotomentosa Hsu et S.C. Cheng (Caprifoliaceae). This paper reports the structural determination of V, a new triterpenoid saponin named Fulvotomentoside A, and characterization of I and II. Fulvotomentoside A, C58H94O26, was obtained as white crystalline needles, mp 215-7 degrees C, [a]D27.5-14.9 degrees (c 0.98, MeOH). Its structure was elucidated to be 3-O-beta-D-xylopyranosyl-(1-3)-alpha-L-rhamnopyranosyl-(1-2)- alpha-L-arabanopyranosyl-hederagenin-28-O-beta-glu cop yranosyl-(1-4)-beta-D- glucopyranoside mainly by spectroscopic analysis (IR, MS, 1H and 13CNMR) and chemical degradation. I, C41H66O12, mp 259-262 degrees C, and II, C46H74O16, mp 222-7 degrees C, were identified to be alpha-hederin and sapindoside B, respectively.
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