Gingerglycolipid ACAS# 145937-22-0 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 145937-22-0 | SDF | Download SDF |
| PubChem ID | 10349562 | Appearance | Powder |
| Formula | C33H56O14 | M.Wt | 676.79 |
| Type of Compound | Aliphatic Compounds | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | [(2S)-2-hydroxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl] (9Z,12Z,15Z)-octadeca-9,12,15-trienoate | ||
| SMILES | CCC=CCC=CCC=CCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)O | ||
| Standard InChIKey | MPSGDHOYFIUPSO-MDAKJLGTSA-N | ||
| Standard InChI | InChI=1S/C33H56O14/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-25(36)43-19-22(35)20-44-32-31(42)29(40)27(38)24(47-32)21-45-33-30(41)28(39)26(37)23(18-34)46-33/h3-4,6-7,9-10,22-24,26-35,37-42H,2,5,8,11-21H2,1H3/b4-3-,7-6-,10-9-/t22-,23-,24-,26+,27+,28+,29+,30-,31-,32-,33+/m1/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. | ||
Gingerglycolipid A Dilution Calculator
Gingerglycolipid A Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 1.4776 mL | 7.3878 mL | 14.7756 mL | 29.5513 mL | 36.9391 mL |
| 5 mM | 0.2955 mL | 1.4776 mL | 2.9551 mL | 5.9103 mL | 7.3878 mL |
| 10 mM | 0.1478 mL | 0.7388 mL | 1.4776 mL | 2.9551 mL | 3.6939 mL |
| 50 mM | 0.0296 mL | 0.1478 mL | 0.2955 mL | 0.591 mL | 0.7388 mL |
| 100 mM | 0.0148 mL | 0.0739 mL | 0.1478 mL | 0.2955 mL | 0.3694 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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Metabolite profiling of the leaves of the Brazilian folk medicine Sideroxylon obtusifolium.[Pubmed:22322398]
Planta Med. 2012 May;78(7):703-10.
Sideroxylon obtusifolium (Roem. & Schult.) T. D. Penn. (family Sapotaceae) is a tree native to Central and South America. Infusions of the bark and the leaves are used in Brazilian folk medicine as an anti-inflammatory remedy. However, information on the constituents of S. obtusifolium remains scarce, and only common pentacyclic triterpenoids have been previously reported. HPLC-DAD/MS analyses revealed that saponins and flavonoids were the main constituents of the leaves. From the butanol-soluble fraction of an ethanolic extract, a total of four saponins and ten flavonol glycosides were isolated by a combination of chromatographic methods including Sephadex LH-20, MPLC, and HPLC. Their structures were established by acid hydrolysis and spectroscopic methods, mainly MS (n), 1D and 2D NMR experiments. The compounds include the new triterpene glycoside 3-O-( beta-D-glucopyranosyl)-protobassic acid 28-O- beta-D-apiofuranosyl-(1 --> 3)-O-[O- beta-D-apiofuranosyl-(1 --> 3)- beta-D-xylopyranosyl-(1 --> 4)]-O- alpha-L-rhamnopyranosyl-(1 --> 2)- alpha-L-arabinopyranosyl ester ( 1), as well as the new flavonol glycosides, quercetin-3-O-(O- alpha-L-rhamnopyranosyl-(1--> 2)-O-[ beta-D-glucopyranosyl-(1 --> 3)]- beta-D-galactopyranoside) ( 6) and kaempferol-3-O-(O- alpha-L-rhamnopyranosyl-(1 --> 2)-O-[ beta-D-glucopyranosyl-(1 --> 3)]- beta-D-galactopyranoside) ( 8). In addition, catechin and a glycerogalactolipid, Gingerglycolipid A, were obtained from the ethyl acetate-soluble fraction. The isolated compounds could be used in the future as chemical markers for quality control of this herbal drug.
[Studies on chemical constituents from roots of Mirabilis jalapa].[Pubmed:18338618]
Zhongguo Zhong Yao Za Zhi. 2008 Jan;33(1):42-6.
OBJECTIVE: To investigate the anti-HIV constituents from the root of Mirabilis jalapa. METHOD: The compounds were isolated by column chromatography on silica gel, Sephadex LH - 20, MCI-gel CHP-20P and RP-18. The structure were identified by means of NMR and MS analyses (1H-NMR, 13C-NMR, MS). RESULT: Eleven compounds were isolated and identified as astragaloside II (1), astragaloside II (2), astragaloside IV (3), astragaloside VI (4), flazin (5), 4'-hydroxy-2, 3-dihydroflavone 7-beta-D-glucopyranoside (6), Gingerglycolipid A (7), 3, 4-dihydroxybenzaldehyd (8), p-hydroxybenzaldehyde (9), beta-sitosterol (10) and daucosterol (11). CONCLUSION: Compounds 1-9 were obtained from this genus for the first time.
