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6alpha-Hydroxylycopodine

CAS# 21061-92-7

6alpha-Hydroxylycopodine

Catalog No. BCN7403----Order now to get a substantial discount!

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6alpha-Hydroxylycopodine: 5mg $886 In Stock
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Quality Control of 6alpha-Hydroxylycopodine

Number of papers citing our products

Chemical structure

6alpha-Hydroxylycopodine

3D structure

Chemical Properties of 6alpha-Hydroxylycopodine

Cas No. 21061-92-7 SDF Download SDF
PubChem ID 21576178 Appearance Powder
Formula C16H25NO2 M.Wt 263.38
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
SMILES CC1CC2C3CCCN4C3(C1)C(CCC4)C(=O)C2O
Standard InChIKey AWIZLLPREQJRKH-GXVXIZHISA-N
Standard InChI InChI=1S/C16H25NO2/c1-10-8-11-12-4-2-6-17-7-3-5-13(15(19)14(11)18)16(12,17)9-10/h10-14,18H,2-9H2,1H3/t10-,11-,12-,13-,14+,16-/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 6alpha-Hydroxylycopodine

The whole plants of Phlegmariurus fargesii.

Biological Activity of 6alpha-Hydroxylycopodine

Description6alpha-Hydroxylycopodine is a natural product from Phlegmariurus fargesii.

Protocol of 6alpha-Hydroxylycopodine

Structure Identification
Chin J Nat Med. 2014 May;12(5):373-6.

A new Lycopodium alkaloid from Phlegmariurus fargesii.[Pubmed: 24856761 ]

To investigate the chemical constituents from the whole plants of Phlegmariurus fargesii.
METHODS AND RESULTS:
Compounds were isolated by repeated silica gel column chromatography. Their structures were elucidated by spectroscopic methods and chemical correlation. The acetylcholinesterase (AChE) inhibitory activity of the isolated compounds was evaluated. A new Lycopodium alkaloid, lycopodine N-oxide (1), along with lycopodine (2), 8,15-dehydrolycopodine (3), 6alpha-Hydroxylycopodine(4), deacetyllycoclavine (5), N-methylhuperzine B (6), lycodine (7), and phlegmarine (8), was isolated.
CONCLUSIONS:
Compound 1 is a new Lycopodium alkaloid, and compound 3 was obtained from nature for the first time. Other alkaloids are isolated from this plant for the first time.

6alpha-Hydroxylycopodine Dilution Calculator

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6alpha-Hydroxylycopodine Molarity Calculator

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Preparing Stock Solutions of 6alpha-Hydroxylycopodine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.7968 mL 18.984 mL 37.968 mL 75.9359 mL 94.9199 mL
5 mM 0.7594 mL 3.7968 mL 7.5936 mL 15.1872 mL 18.984 mL
10 mM 0.3797 mL 1.8984 mL 3.7968 mL 7.5936 mL 9.492 mL
50 mM 0.0759 mL 0.3797 mL 0.7594 mL 1.5187 mL 1.8984 mL
100 mM 0.038 mL 0.1898 mL 0.3797 mL 0.7594 mL 0.9492 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 6alpha-Hydroxylycopodine

A new Lycopodium alkaloid from Phlegmariurus fargesii.[Pubmed:24856761]

Chin J Nat Med. 2014 May;12(5):373-6.

AIM: To investigate the chemical constituents from the whole plants of Phlegmariurus fargesii. METHOD: Compounds were isolated by repeated silica gel column chromatography. Their structures were elucidated by spectroscopic methods and chemical correlation. The acetylcholinesterase (AChE) inhibitory activity of the isolated compounds was evaluated. RESULTS: A new Lycopodium alkaloid, lycopodine N-oxide (1), along with lycopodine (2), 8,15-dehydrolycopodine (3), 6alpha-Hydroxylycopodine (4), deacetyllycoclavine (5), N-methylhuperzine B (6), lycodine (7), and phlegmarine (8), was isolated. CONCLUSION: Compound 1 is a new Lycopodium alkaloid, and compound 3 was obtained from nature for the first time. Other alkaloids are isolated from this plant for the first time.

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