Marsdenoside ACAS# 858360-56-2 |
Quality Control & MSDS
Package In Stock
Number of papers citing our products
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Cas No. | 858360-56-2 | SDF | Download SDF |
PubChem ID | N/A | Appearance | Powder |
Formula | C45H70O14 | M.Wt | 835.03 |
Type of Compound | Other Steroids | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
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. |
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Marsdenoside A Dilution Calculator
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Marsdenoside A Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 1.1976 mL | 5.9878 mL | 11.9756 mL | 23.9512 mL | 29.939 mL |
5 mM | 0.2395 mL | 1.1976 mL | 2.3951 mL | 4.7902 mL | 5.9878 mL |
10 mM | 0.1198 mL | 0.5988 mL | 1.1976 mL | 2.3951 mL | 2.9939 mL |
50 mM | 0.024 mL | 0.1198 mL | 0.2395 mL | 0.479 mL | 0.5988 mL |
100 mM | 0.012 mL | 0.0599 mL | 0.1198 mL | 0.2395 mL | 0.2994 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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University of Minnesota
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Harvard University
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Colorado State University
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Auburn University
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Yale University
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Worcester Polytechnic Institute
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Washington State University
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Stanford University
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University of Leipzig
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The Institute of Cancer Research
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Heidelberg University
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University of Amsterdam
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TsingHua University
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Jilin University
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The cytotoxic and tyrosine kinase inhibitory properties of C21 steroids and iridoids from the tubers of Alocasia cucullata.[Pubmed:27120176]
J Nat Med. 2016 Jul;70(3):602-9.
Ten steroids and iridoids were isolated from the tubers of Alocasia cucullata (Lour.) G. Don. Among them, alocasgenin A (1) and alocasgenoside B-C (2-3) were new compounds and the aglycone of compound 1, obtained from the acid hydrolysis of 1, was named alocasgenol (1a). Also, for the first time, tenacigenin B (4), 17beta-tenacigenin-B (5), 3-O-6-deoxy-3-O-methyl-beta-D-allopyranosyl-(1-->4)-beta-D-oleandropyranosyl-tenacigenin C (6), Marsdenoside A-B (7-8) and tenacigenoside A-B (9-10) were isolated from the genus Alocasia. The chemical structures were elucidated by the extensive analysis of spectral data and compared with the literature. By evaluation of the cytotoxic and tyrosine kinase inhibition, compounds 1-10, 1a and compound 2 showed significant growth inhibition against two tumour cell lines, MGC-803 and HT-29, while compounds 1, 1a, 3, 6 and 8 presented moderate inhibition. Furthermore, compound 2 had the inhibitory property against the enzyme activity biochemically.
[C21 steroids from the stems of Marsdenia tenacissima].[Pubmed:18717339]
Yao Xue Xue Bao. 2008 May;43(5):509-12.
To study the C21 steroids of the stems of Marsdenia tenacissima (Roxb.) Wight et Arn, various chromatography methods were used for the isolation of the constituents and their structures were identified by spectral analysis. Eight C21 steroids were isolated from the CHCl3 extract, which were identified as 11alpha-O-tigloyl-17beta-tenacigenin B (1), 17beta-tenacigenin B (2), tenacigenoside A (3), 11alpha-O-2-methylbutyryl-12beta-O-acetyl tenacigenin B (4), tenacissoside H (5), Marsdenoside A (6), tenacissoside G (7), and tenacissoside I (8). Among them, compound 1 is a new compound.