Lucyoside BCAS# 91174-19-5 |
2D Structure
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
Cas No. | 91174-19-5 | SDF | Download SDF |
PubChem ID | 13518118 | Appearance | Powder |
Formula | C42H68O15 | M.Wt | 812.99 |
Type of Compound | Triterpenoids | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | [(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-11-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate | ||
SMILES | CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC6C(C(C(C(O6)CO)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C | ||
Standard InChIKey | ZUILGDNVKPMVIA-QDZACNFGSA-N | ||
Standard InChI | InChI=1S/C42H68O15/c1-37(2)11-13-42(36(53)57-35-32(52)30(50)28(48)24(18-44)55-35)14-12-40(5)20(21(42)15-37)7-8-26-38(3)16-22(46)33(39(4,19-45)25(38)9-10-41(26,40)6)56-34-31(51)29(49)27(47)23(17-43)54-34/h7,21-35,43-52H,8-19H2,1-6H3/t21-,22+,23+,24+,25+,26+,27+,28+,29-,30-,31+,32+,33-,34-,35-,38-,39-,40+,41+,42-/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. |
Description | Lucyoside B is a natural product from Luffa cylindrica ROEM. |
Structure Identification | Yakugaku Zasshi Journal of the Pharmaceutical Society of Japan, 1984, 104(3):246.Studies on the Constituents of Cucurbitaceae Plants. VI. On the Saponin Constituents of Luffa cylindrica ROEM.(1) [Reference: WebLink]
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Lucyoside B Dilution Calculator
Lucyoside B Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 1.23 mL | 6.1501 mL | 12.3003 mL | 24.6005 mL | 30.7507 mL |
5 mM | 0.246 mL | 1.23 mL | 2.4601 mL | 4.9201 mL | 6.1501 mL |
10 mM | 0.123 mL | 0.615 mL | 1.23 mL | 2.4601 mL | 3.0751 mL |
50 mM | 0.0246 mL | 0.123 mL | 0.246 mL | 0.492 mL | 0.615 mL |
100 mM | 0.0123 mL | 0.0615 mL | 0.123 mL | 0.246 mL | 0.3075 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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Studies on the Constituents of Cucurbitaceae Plants. VI. On the Saponin Constituents of Luffa cylindrica ROEM.(1)
Yakugaku Zasshi Journal of the Pharmaceutical Society of Japan, 1984, 104(3):246.
New saponins, named lucyoside A (1),Lucyoside B (2), lucyoside C (3), lucyoside D (4), lucyoside E (5), lucyoside F (6),lucyoside G (7),lucyoside H (8), besides known ginsenosides-Re (9) and -Rg_1 (10), were isolated from herb of Luffa cylindrica ROEM.. On methanolysis 1,2,3,5,7 and 8 yielded methyl 21β-hydroxyhederagenin (11), arjunolic acid (12), methyl machaerinate (13), hederagenin (14), maslinic acid (15) and oleanolic acid (17), respectively. The structures of 1-8 were elucidated mainly mass, ^<13>C-nuclear magnetic resonance and ^1H-nuclear magnetic resonance spectroscopy.