Ilexoside XLVIIICAS# 129095-76-7 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
Cas No. | 129095-76-7 | SDF | Download SDF |
PubChem ID | 14564471.0 | Appearance | Powder |
Formula | C42H66O15 | M.Wt | 810.98 |
Type of Compound | Triterpenoids | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | (2S,3S,4S,5R,6R)-6-[[(3S,4R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid | ||
SMILES | CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C | ||
Standard InChIKey | RZQHWSDMLZHIRN-ZJDNFKTFSA-N | ||
Standard InChI | InChI=1S/C42H66O15/c1-37(2)13-15-42(36(53)57-34-30(49)27(46)26(45)22(18-43)54-34)16-14-40(5)20(21(42)17-37)7-8-24-38(3)11-10-25(39(4,19-44)23(38)9-12-41(24,40)6)55-35-31(50)28(47)29(48)32(56-35)33(51)52/h7,21-32,34-35,43-50H,8-19H2,1-6H3,(H,51,52)/t21-,22+,23+,24+,25-,26+,27-,28-,29-,30+,31+,32-,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. |
||
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. |
||
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. |
Ilexoside XLVIII Dilution Calculator
Ilexoside XLVIII Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 1.2331 mL | 6.1654 mL | 12.3308 mL | 24.6615 mL | 30.8269 mL |
5 mM | 0.2466 mL | 1.2331 mL | 2.4662 mL | 4.9323 mL | 6.1654 mL |
10 mM | 0.1233 mL | 0.6165 mL | 1.2331 mL | 2.4662 mL | 3.0827 mL |
50 mM | 0.0247 mL | 0.1233 mL | 0.2466 mL | 0.4932 mL | 0.6165 mL |
100 mM | 0.0123 mL | 0.0617 mL | 0.1233 mL | 0.2466 mL | 0.3083 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. |
Calcutta University
University of Minnesota
University of Maryland School of Medicine
University of Illinois at Chicago
The Ohio State University
University of Zurich
Harvard University
Colorado State University
Auburn University
Yale University
Worcester Polytechnic Institute
Washington State University
Stanford University
University of Leipzig
Universidade da Beira Interior
The Institute of Cancer Research
Heidelberg University
University of Amsterdam
University of Auckland
TsingHua University
The University of Michigan
Miami University
DRURY University
Jilin University
Fudan University
Wuhan University
Sun Yat-sen University
Universite de Paris
Deemed University
Auckland University
The University of Tokyo
Korea University
- Ajuforrestin B
Catalog No.:BCX1334
CAS No.:708277-48-9
- Pseudoginsenoside F8
Catalog No.:BCX1333
CAS No.:69884-01-1
- β-D-Glucopyranoside, (3β,12β)-20-[(6-O-α-L-arabinofuranosyl-β-D-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl 2-O-β-D-glucopyranosyl-, 6-acetate
Catalog No.:BCX1332
CAS No.:1613477-95-4
- Pseudoginsenoside RC1
Catalog No.:BCX1331
CAS No.:102805-32-3
- Quinquenoside III
Catalog No.:BCX1330
CAS No.:208764-53-8
- Multiflorin A
Catalog No.:BCX1329
CAS No.:1350028-90-8
- Multiflorin B
Catalog No.:BCX1328
CAS No.:52657-01-9
- 6-Methylrhein
Catalog No.:BCX1327
CAS No.:401621-27-0
- Methyllycaconitine
Catalog No.:BCX1326
CAS No.:21019-30-7
- Lycaconitine
Catalog No.:BCX1325
CAS No.:25867-19-0
- Anhydronotoptol
Catalog No.:BCX1324
CAS No.:88206-51-3
- Decuroside V
Catalog No.:BCX1323
CAS No.:96648-59-8
- Gosferol
Catalog No.:BCX1336
CAS No.:37551-62-5
- rel-(+)-(1R,2Z,7Z,10S,11S)-10-(Acetyloxy)-7,12,12-trimethylbicyclo[9.1.0]dodeca-2,7-dien-4-one
Catalog No.:BCX1337
CAS No.:886439-01-6
- Phloyoside I
Catalog No.:BCX1338
CAS No.:139757-58-7
- Dracaenoside F
Catalog No.:BCX1339
CAS No.:109460-83-5
- Linderanine C
Catalog No.:BCX1340
CAS No.:139681-96-2
- Paratocarpin K
Catalog No.:BCX1341
CAS No.:170900-13-7
- 3'-Methoxycoumestrol
Catalog No.:BCX1342
CAS No.:13360-66-2
- 8-Geranyl daidzein
Catalog No.:BCX1343
CAS No.:1072940-16-9
- 6β-Hydroxy-7-epiloganin
Catalog No.:BCX1344
CAS No.:125410-28-8
- 9-epi-Phlomiol
Catalog No.:BCX1345
CAS No.:1621720-47-5
- 5, 9-epi-Phlomiol
Catalog No.:BCX1346
CAS No.:1621908-70-0
- 8-Formylophiopogonone B
Catalog No.:BCX1347
CAS No.:1316224-74-4
Triterpenoid saponins from Ilex kudincha.[Pubmed:10479318]
J Nat Prod. 1999 Aug;62(8):1128-33.
Ten new triterpene saponins, ilekudinosides A-J (2, 6-8, 10, 13-17), together with seven known triterpene saponins, Ilexoside XLVIII (1); cynarasaponin C (5); latifolosides A (9), C (3), G (12), and H (4); and kudinoside G (11), were isolated from an aqueous extract of the leaves of Ilex kudincha. They possessed oleanane- and ursane-type triterpenoids as the aglycons. The structures were elucidated by 1D and 2D NMR experiments, including ROE difference, HOHAHA difference, 1H-1H COSY, and 1H-13C COSY (HMQC, HMBC) methods and sugar analysis. Compounds 1 and 5 exhibited acyl CoA cholesteryl acyl transferase (ACAT) inhibitory activity.