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1beta-Hydroxy-beta-eudesmol

CAS# 83217-89-4

1beta-Hydroxy-beta-eudesmol

Catalog No. BCN7097----Order now to get a substantial discount!

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Quality Control of 1beta-Hydroxy-beta-eudesmol

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Chemical structure

1beta-Hydroxy-beta-eudesmol

3D structure

Chemical Properties of 1beta-Hydroxy-beta-eudesmol

Cas No. 83217-89-4 SDF Download SDF
PubChem ID 13969455 Appearance Powder
Formula C15H26O2 M.Wt 238.37
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (1R,4aS,6R,8aR)-6-(2-hydroxypropan-2-yl)-8a-methyl-4-methylidene-1,2,3,4a,5,6,7,8-octahydronaphthalen-1-ol
SMILES CC12CCC(CC1C(=C)CCC2O)C(C)(C)O
Standard InChIKey MQOLOUZWNJHZLN-QVHKTLOISA-N
Standard InChI InChI=1S/C15H26O2/c1-10-5-6-13(16)15(4)8-7-11(9-12(10)15)14(2,3)17/h11-13,16-17H,1,5-9H2,2-4H3/t11-,12+,13-,15-/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.
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 1beta-Hydroxy-beta-eudesmol

The herbs of Cymbopogon proximus STAPF.

Biological Activity of 1beta-Hydroxy-beta-eudesmol

Description1beta-Hydroxy-beta-eudesmol is a natural product from Cymbopogon proximus STAPF.

Protocol of 1beta-Hydroxy-beta-eudesmol

Structure Identification
Molecules, 2003, 8(9):670-677.

Sesquiterpenes from Cymbopogon proximus.[Reference: WebLink]


METHODS AND RESULTS:
In addition to four previously reported compounds: proximadiol (1), 5α-hydroxy-β-eudesmol (2), 1beta-Hydroxy-beta-eudesmol (4) and 1β-hydroxy-α-eudesmol (5), two new sesquiterpenes, 5α-hydroperoxy-β-eudesmol (3) and 7α,11-dihydroxycadin-10(14)-ene (6) were isolated from the unsaponifiable fraction of the petroleum ether extract of Cymbopogon proximus STAPF.
CONCLUSIONS:
Isolation of compounds 2, 4 and 5 from the genus Cymbopogon is reported for the first time. The structure elucidation of these compounds was based primarily on 1D and 2D-NMR analyses.

1beta-Hydroxy-beta-eudesmol Dilution Calculator

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Preparing Stock Solutions of 1beta-Hydroxy-beta-eudesmol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.1952 mL 20.9758 mL 41.9516 mL 83.9032 mL 104.879 mL
5 mM 0.839 mL 4.1952 mL 8.3903 mL 16.7806 mL 20.9758 mL
10 mM 0.4195 mL 2.0976 mL 4.1952 mL 8.3903 mL 10.4879 mL
50 mM 0.0839 mL 0.4195 mL 0.839 mL 1.6781 mL 2.0976 mL
100 mM 0.042 mL 0.2098 mL 0.4195 mL 0.839 mL 1.0488 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 1beta-Hydroxy-beta-eudesmol

Two New Eudesmane Sesquiterpenoids from the Flowers of Chrysanthemum indicum.[Pubmed:30820878]

Nat Prod Bioprospect. 2019 Apr;9(2):145-148.

The flowers of Chrysanthemum indicum, i.e. Ye-ju-hua recorded in the Chinese Pharmacopoeia, has been widely used in China as an important heat-clearing and detoxifying herb for the treatment of inflammation, headache, and vertigo. A phytochemical investigation of this herb has led to the isolation of two new eudesmane sesquiterpenoids, 7-epi-eudesm-4(15),11(13)-diene-1beta,3beta-diol (1) and 7-epi-1beta-Hydroxy-beta-eudesmol (2). The molecular structures of these new sesquiterpenoids were established based on the comprehensive spectroscopic analyses, including NMR, MS, and IR, and comparing with the literatures.

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