Homalomenol A

CAS# 145400-03-9

Homalomenol A

2D Structure

Catalog No. BCN1647----Order now to get a substantial discount!

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Quality Control of Homalomenol A

3D structure

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Homalomenol A

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Chemical Properties of Homalomenol A

Cas No. 145400-03-9 SDF Download SDF
PubChem ID 91884956 Appearance Oil
Formula C15H26O2 M.Wt 238.4
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (3R,3aR,4S,7R,7aR)-4,7a-dimethyl-3-(2-methylprop-1-enyl)-2,3,3a,5,6,7-hexahydro-1H-indene-4,7-diol
SMILES CC(=CC1CCC2(C1C(CCC2O)(C)O)C)C
Standard InChIKey FKMCEEHVCIIPLE-ZSAUSMIDSA-N
Standard InChI InChI=1S/C15H26O2/c1-10(2)9-11-5-7-14(3)12(16)6-8-15(4,17)13(11)14/h9,11-13,16-17H,5-8H2,1-4H3/t11-,12-,13-,14+,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 Homalomenol A

The roots of Homalomena aromatica.

Protocol of Homalomenol A

Structure Identification
Phytochemistry. 1992 Oct;31(10):3515-20.

Sesquiterpenoids from the roots of Homalomena aromatica.[Pubmed: 1368861]


METHODS AND RESULTS:
From roots of Homalomena aromatica three new sesquiterpene alcohols, 1 beta, 4 beta, 7 alpha-trihydroxyeudesmane, Homalomenol A, and homalomenol B were isolated together with oplopanone, oplodiol and bullatantriol.
CONCLUSIONS:
The structures of the new constituents were elucidated by spectroscopic investigations and chemical transformations.

Homalomenol A Dilution Calculator

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Preparing Stock Solutions of Homalomenol A

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.1946 mL 20.9732 mL 41.9463 mL 83.8926 mL 104.8658 mL
5 mM 0.8389 mL 4.1946 mL 8.3893 mL 16.7785 mL 20.9732 mL
10 mM 0.4195 mL 2.0973 mL 4.1946 mL 8.3893 mL 10.4866 mL
50 mM 0.0839 mL 0.4195 mL 0.8389 mL 1.6779 mL 2.0973 mL
100 mM 0.0419 mL 0.2097 mL 0.4195 mL 0.8389 mL 1.0487 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 Homalomenol A

Sesquiterpene components from the flower buds ofMagnolia fargesii.[Pubmed:18975180]

Arch Pharm Res. 1997 Aug;20(4):363-7.

From the Chinese crude drugshin-i, the flower buds ofMagnolia fargesii, four sesquiterpene, oplopanone (1), oplodiol (2), Homalomenol A (3) and 1beta,4beta,7alpha-trihydroxyeudesmane (4) were isolated. These structures were elucidated and the(13)C-NMR chemical, shifts of these compounds were revised by means of various 2D-NMR techniques.

Sesquiterpenoids from the roots of Homalomena aromatica.[Pubmed:1368861]

Phytochemistry. 1992 Oct;31(10):3515-20.

From roots of Homalomena aromatica three new sesquiterpene alcohols, 1 beta, 4 beta, 7 alpha-trihydroxyeudesmane, Homalomenol A, and homalomenol B were isolated together with oplopanone, oplodiol and bullatantriol. The structures of the new constituents were elucidated by spectroscopic investigations and chemical transformations.

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