Microstegiol

CAS# 143246-41-7

Microstegiol

Catalog No. BCN3157----Order now to get a substantial discount!

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Microstegiol: 5mg Please Inquire In Stock
Microstegiol: 10mg Please Inquire In Stock
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Quality Control of Microstegiol

Number of papers citing our products

Chemical structure

Microstegiol

3D structure

Chemical Properties of Microstegiol

Cas No. 143246-41-7 SDF Download SDF
PubChem ID 403772 Appearance Powder
Formula C20H26O2 M.Wt 298.4
Type of Compound Diterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
SMILES CC1=C2CCCC(C3(C2=C(C=C1)C=C(C3=O)C(C)C)O)(C)C
Standard InChIKey KIXMQGXACFNMEM-FQEVSTJZSA-N
Standard InChI InChI=1S/C20H26O2/c1-12(2)16-11-14-9-8-13(3)15-7-6-10-19(4,5)20(22,17(14)15)18(16)21/h8-9,11-12,22H,6-7,10H2,1-5H3/t20-/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.

Source of Microstegiol

The roots of Salvia prionitis

Biological Activity of Microstegiol

Description1. Migrostegiol has a little activity against B. subtilis.
TargetsAntifection

Microstegiol Dilution Calculator

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Microstegiol Molarity Calculator

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Preparing Stock Solutions of Microstegiol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.3512 mL 16.756 mL 33.5121 mL 67.0241 mL 83.7802 mL
5 mM 0.6702 mL 3.3512 mL 6.7024 mL 13.4048 mL 16.756 mL
10 mM 0.3351 mL 1.6756 mL 3.3512 mL 6.7024 mL 8.378 mL
50 mM 0.067 mL 0.3351 mL 0.6702 mL 1.3405 mL 1.6756 mL
100 mM 0.0335 mL 0.1676 mL 0.3351 mL 0.6702 mL 0.8378 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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References on Microstegiol

Components and antibacterial activity of the roots of Salvia jaminiana.[Pubmed:15893885]

Fitoterapia. 2005 Jul;76(5):450-2.

The acetone extract of the roots of Salvia jaminiana, containing the sterols campestanol, stigmasterol and sitosterol, and five known diterpenoids, ferruginol, cryptanol, 6,7-dehydroroyleanon, 6-hydroxysalvinolone and Microstegiol, remarkably inhibited the growth of Bacillus subtilis, Staphylococcus aureus ATCC 25923 and Streptococcus alpha-hemolitic.

Antibacterial diterpenes from the roots of Salvia viridis.[Pubmed:10909268]

Planta Med. 2000 Jun;66(5):458-62.

Three new diterpenes, salviviridinol, viridinol, viridone, five known diterpenes, sugiol, 1-oxoferruginol, ferruginol, aethiopinone and Microstegiol, abietane and rearranged abietane diterpenes were isolated from the roots of Salvia viridis. These compounds were assayed against S. aureus ATCC 6538 P, E. coli ATCC 8739, P. mirabilis ATCC 14153, K. pneumonia ATCC 4352, P. aeruginosa ATCC 27853, S. epidermidis ATCC 12228, E. faecalis ATCC 29212 and a yeast C. albicans ATCC 10231. 1-Oxoferruginol showed activity against B. subtilis, S. aureus, S. epidermidis and a modest activity against P. mirabilis, migrostegiol had a little activity against B. subtilis. The structures of the compounds were established by 1D and 2D NMR spectroscopic techniques.

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