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6,7-Dehydroferruginol

CAS# 34539-84-9

6,7-Dehydroferruginol

Catalog No. BCN3218----Order now to get a substantial discount!

Product Name & Size Price Stock
6,7-Dehydroferruginol: 5mg $725 In Stock
6,7-Dehydroferruginol: 10mg Please Inquire In Stock
6,7-Dehydroferruginol: 20mg Please Inquire Please Inquire
6,7-Dehydroferruginol: 50mg Please Inquire Please Inquire
6,7-Dehydroferruginol: 100mg Please Inquire Please Inquire
6,7-Dehydroferruginol: 200mg Please Inquire Please Inquire
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Quality Control of 6,7-Dehydroferruginol

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Chemical structure

6,7-Dehydroferruginol

3D structure

Chemical Properties of 6,7-Dehydroferruginol

Cas No. 34539-84-9 SDF Download SDF
PubChem ID 10978982 Appearance Powder
Formula C20H28O M.Wt 284.4
Type of Compound Diterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (4bS,8aS)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthren-3-ol
SMILES CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)O
Standard InChIKey NCHINJPZLGMLCY-AZUAARDMSA-N
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 6,7-Dehydroferruginol

The herbs of Cunninghamia lanceolata

Biological Activity of 6,7-Dehydroferruginol

Description1. 6,7-Dehydroferruginol has potent activity against F. palustris . 2. 6,7-Dehydroferruginol and sugiol are weakly active against Heterosigma akashiwo.
TargetsAntifection

6,7-Dehydroferruginol Dilution Calculator

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6,7-Dehydroferruginol Molarity Calculator

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Preparing Stock Solutions of 6,7-Dehydroferruginol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.5162 mL 17.5809 mL 35.1617 mL 70.3235 mL 87.9044 mL
5 mM 0.7032 mL 3.5162 mL 7.0323 mL 14.0647 mL 17.5809 mL
10 mM 0.3516 mL 1.7581 mL 3.5162 mL 7.0323 mL 8.7904 mL
50 mM 0.0703 mL 0.3516 mL 0.7032 mL 1.4065 mL 1.7581 mL
100 mM 0.0352 mL 0.1758 mL 0.3516 mL 0.7032 mL 0.879 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 6,7-Dehydroferruginol

Antifungal abietane-type diterpenes from the cones of Taxodium distichum Rich.[Pubmed:21072573]

J Chem Ecol. 2010 Dec;36(12):1381-6.

The chemical composition of Taxodium distichum cones and the antifungal activities of twelve diterpenoids against two wood decay fungi, Trametes versicolor (white-rot) and Fomitopsis palustris (brown-rot) were examined. The chemical composition of the major extractive fraction, the n-C(6)H(14) extract, was evaluated and its antifungal properties were identified. Twelve diterpenoids including ten abietane-type components were isolated from the n-C(6)H(14) extract: 6,7-Dehydroferruginol (1), ferruginol (2), 6,7-dehydroroyleanone (3), sandaracopimaric acid (4), taxodione (5), taxodal (6), taxodone (7), sugiol (8), xanthoperol (9), salvinolone (10), 5,6-dehydrosugiol (11), and 14-deoxycoleon U (12). Compounds 5 and 12 were highly active against both wood-decay fungi. In particular, the activities of these compounds against F. palustris were potent. The results suggest that the position and the number of hydroxyl groups on abietane-type structures may be related to antifungal activities against T. versicolor and F. palustris.

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