VogelosideCAS# 60077-47-6 |
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| Cas No. | 60077-47-6 | SDF | Download SDF |
| PubChem ID | 101939796 | Appearance | Powder |
| Formula | C17H24O10 | M.Wt | 388.37 |
| Type of Compound | Iridoids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | 5-ethenyl-3-methoxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-1-one | ||
| SMILES | COC1CC2C(C(OC=C2C(=O)O1)OC3C(C(C(C(O3)CO)O)O)O)C=C | ||
| Standard InChIKey | RAYZRCGMIDUTKS-CMVXZMDTSA-N | ||
| Standard InChI | InChI=1S/C17H24O10/c1-3-7-8-4-11(23-2)26-15(22)9(8)6-24-16(7)27-17-14(21)13(20)12(19)10(5-18)25-17/h3,6-8,10-14,16-21H,1,4-5H2,2H3/t7?,8?,10-,11?,12-,13+,14-,16?,17+/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. | ||
The herbs of Anthocleista vogelii
| Description | 1. Vogeloside shows inhibition of nitric oxide production in lipopolysaccharide-activated macrophages; its activity is comparable to that of aminoguanidine, a classic inhibitor. |
| Targets | NO |
Vogeloside Dilution Calculator
Vogeloside Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 2.5749 mL | 12.8743 mL | 25.7486 mL | 51.4973 mL | 64.3716 mL |
| 5 mM | 0.515 mL | 2.5749 mL | 5.1497 mL | 10.2995 mL | 12.8743 mL |
| 10 mM | 0.2575 mL | 1.2874 mL | 2.5749 mL | 5.1497 mL | 6.4372 mL |
| 50 mM | 0.0515 mL | 0.2575 mL | 0.515 mL | 1.0299 mL | 1.2874 mL |
| 100 mM | 0.0257 mL | 0.1287 mL | 0.2575 mL | 0.515 mL | 0.6437 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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Modified secoiridoid from Acicarpha tribuloides and inhibition of nitric oxide production in LPS-activated macrophages.[Pubmed:16808936]
Phytochemistry. 2006 Jul;67(14):1534-8.
Bioassay-guided fractionation of Acicarpha tribuloides Juss. resulted in the isolation of an uncommon non-glycosylated secoiridoid, tribulolide (1), two known secoiridoid glycosides named secologanic acid (2) and Vogeloside (3) as well as two natural chromones, 6,7-dimethoxychromone (4) and 7-hydroxy-6-methoxy-chromone (5). Compounds 1-3 showed inhibition of nitric oxide production in lipopolysaccharide-activated macrophages; their activity is comparable to that of aminoguanidine, a classic inhibitor.
[Terpenoid glycosides from stem of Luculia pinceana].[Pubmed:18338598]
Zhongguo Zhong Yao Za Zhi. 2007 Dec;32(24):2606-9.
OBJECTIVE: To study the chemical constituents from n-BuOH portion of ethanolic extract from the stem of Luculia pinceana. METHOD: The column chromatographic techniques were applied to isolate constituents. A combination of IR, FAB-MS, NMR and 2D NMR spectroscopy was used to identify structures. RESULT: Seven compounds were isolated from the n-BuOH fraction and their structures were elucidated as Vogeloside (1), epi-Vogeloside (2), loganoside (3), loganin (4), cincholic acid 28-O-beta-D-glucopyranosyl ester (5), cincholic acid-3-O-beta-D-glucopyranoside, 28-O-beta-D-glucopyranosyl ester (6), cincholic acid-3-O-beta-D-glucopyranoside (7). CONCLUSION: Compounds 1-7 were isolated from the genus for the first time.
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