Drahebenine

CAS# 1399049-43-4

Drahebenine

Catalog No. BCN7044----Order now to get a substantial discount!

Product Name & Size Price Stock
Drahebenine: 5mg $799 In Stock
Drahebenine: 10mg Please Inquire In Stock
Drahebenine: 20mg Please Inquire Please Inquire
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Drahebenine: 500mg Please Inquire Please Inquire
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Quality Control of Drahebenine

Number of papers citing our products

Chemical structure

Drahebenine

3D structure

Chemical Properties of Drahebenine

Cas No. 1399049-43-4 SDF Download SDF
PubChem ID 136807960 Appearance Powder
Formula C13H16N2O2 M.Wt 232.28
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 2-methoxy-4-(2,2,5-trimethylimidazol-4-yl)phenol
SMILES CC1=NC(N=C1C2=CC(=C(C=C2)O)OC)(C)C
Standard InChIKey UBDFYAAYCZNGLQ-UHFFFAOYSA-N
Standard InChI InChI=1S/C13H16N2O2/c1-8-12(15-13(2,3)14-8)9-5-6-10(16)11(7-9)17-4/h5-7,16H,1-4H3
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 Drahebenine

The aerial parts of Dracocephalum heterophyllum.

Biological Activity of Drahebenine

DescriptionDrahebenine is a natural product from Daphniphyllum longeracemosum.

Protocol of Drahebenine

Structure Identification
Phytochemistry. 2012 Oct;82:166-71.

Phenolic alkaloids from the aerial parts of Dracocephalum heterophyllum.[Pubmed: 22800911 ]


METHODS AND RESULTS:
Chemical examination of aerial parts of Dracocephalum heterophyllum resulted in isolation of phenolic alkaloids, including two flavonoidal alkaloids, drahebephins A and B, one imidazole alkaloid with a phenolic substituent, Drahebenine, together with 15 other known compounds. Their structures were established by extensive spectroscopic data analyses. Due to the stereogenic center in the pyrrolidin-2-one ring, the flavonoidal alkaloids are chiral, although they were isolated as racemates. The enantiomers were separated by HPLC using a chiral phase and stereochemically characterized by circular dichroism (CD) spectroscopy.
CONCLUSIONS:
The structure of compound Drahebenine was established by X-ray crystallography.

Drahebenine Dilution Calculator

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Drahebenine Molarity Calculator

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Preparing Stock Solutions of Drahebenine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.3051 mL 21.5257 mL 43.0515 mL 86.103 mL 107.6287 mL
5 mM 0.861 mL 4.3051 mL 8.6103 mL 17.2206 mL 21.5257 mL
10 mM 0.4305 mL 2.1526 mL 4.3051 mL 8.6103 mL 10.7629 mL
50 mM 0.0861 mL 0.4305 mL 0.861 mL 1.7221 mL 2.1526 mL
100 mM 0.0431 mL 0.2153 mL 0.4305 mL 0.861 mL 1.0763 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 Drahebenine

Phenolic alkaloids from the aerial parts of Dracocephalum heterophyllum.[Pubmed:22800911]

Phytochemistry. 2012 Oct;82:166-71.

Chemical examination of aerial parts of Dracocephalum heterophyllum resulted in isolation of phenolic alkaloids, including two flavonoidal alkaloids, drahebephins A and B, one imidazole alkaloid with a phenolic substituent, Drahebenine, together with 15 other known compounds. Their structures were established by extensive spectroscopic data analyses. Due to the stereogenic center in the pyrrolidin-2-one ring, the flavonoidal alkaloids are chiral, although they were isolated as racemates. The enantiomers were separated by HPLC using a chiral phase and stereochemically characterized by circular dichroism (CD) spectroscopy. The structure of compound Drahebenine was established by X-ray crystallography.

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