Stigmastane-3,6-dioneCAS# 22149-69-5 |
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| Cas No. | 22149-69-5 | SDF | Download SDF |
| PubChem ID | 13992093 | Appearance | Powder |
| Formula | C29H48O2 | M.Wt | 428.7 |
| Type of Compound | Steroids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | (8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,4,5,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,6-dione | ||
| SMILES | CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CCC(=O)C4)C)C)C(C)C | ||
| Standard InChIKey | HMMVBUVVQLUGQA-KSYQFOCASA-N | ||
| Standard InChI | InChI=1S/C29H48O2/c1-7-20(18(2)3)9-8-19(4)23-10-11-24-22-17-27(31)26-16-21(30)12-14-29(26,6)25(22)13-15-28(23,24)5/h18-20,22-26H,7-17H2,1-6H3/t19-,20-,22+,23-,24+,25+,26?,28-,29-/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 roots of Piper nigrum
| Description | 1. Stigmastane-3,6-dione has anti-inflammatory activity. 2. 5 alpha-Stigmastane-3,6-dione shows antifeedant activity against bell weevils. |
| Targets | Immunology & Inflammation related |
Stigmastane-3,6-dione Dilution Calculator
Stigmastane-3,6-dione Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 2.3326 mL | 11.6632 mL | 23.3263 mL | 46.6527 mL | 58.3158 mL |
| 5 mM | 0.4665 mL | 2.3326 mL | 4.6653 mL | 9.3305 mL | 11.6632 mL |
| 10 mM | 0.2333 mL | 1.1663 mL | 2.3326 mL | 4.6653 mL | 5.8316 mL |
| 50 mM | 0.0467 mL | 0.2333 mL | 0.4665 mL | 0.9331 mL | 1.1663 mL |
| 100 mM | 0.0233 mL | 0.1166 mL | 0.2333 mL | 0.4665 mL | 0.5832 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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Triterpenoid profile of flower and leaf cuticular waxes of heather Calluna vulgaris.[Pubmed:23148482]
Nat Prod Res. 2013 Aug;27(15):1404-7.
Analysis of the main triterpenoid profile of chloroform-soluble cuticular waxes of heather flowers and leaves by GC-MS revealed the following composition: five triterpene acids - betulinic, oleanolic, ursolic, 3-oxo-olean-12-en-28-oic and 3-oxo-ursan-12-en-28-oic; eight monohydroxyalcohols - alpha-amyrin, beta-amyrin, cycloartanol, 24-methylenecycloartanol, friedelinol, germanicol, lupeol and taraxasterol; three dihydroxyalcohols - betulin, erythrodiol and uvaol; two aldehydes - oleanolic and ursolic; four ketones - alpha-amyrenone, 4-epi-friedelin, friedelin and taraxerone and seven steroids - campesterol, cholesterol, sitostanol, sitosterol, stigmasterol, stigmasta-3,5-dien-7-one and Stigmastane-3,6-dione. Triterpenoids accounted for 20% and 65% by mass of flower and leaf waxes, respectively, which suggest that heather leaves represent a very promising source of these compounds. Ursolic acid was the principal triterpenoid in the cuticular wax of both organs, whereas among the neutral triterpenes, friedelin and uvaol were the most abundant in flowers and leaves, respectively. This report provides the first thorough overview of the triterpenoid composition of cuticular waxes of heather.
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