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Dehydrocrenatine

CAS# 26585-13-7

Dehydrocrenatine

Catalog No. BCN5147----Order now to get a substantial discount!

Product Name & Size Price Stock
Dehydrocrenatine: 5mg $690 In Stock
Dehydrocrenatine: 10mg Please Inquire In Stock
Dehydrocrenatine: 20mg Please Inquire Please Inquire
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Dehydrocrenatine: 200mg Please Inquire Please Inquire
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Quality Control of Dehydrocrenatine

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Chemical structure

Dehydrocrenatine

3D structure

Chemical Properties of Dehydrocrenatine

Cas No. 26585-13-7 SDF Download SDF
PubChem ID 179485 Appearance Yellow powder
Formula C14H12N2O M.Wt 224.3
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 1-ethenyl-4-methoxy-9H-pyrido[3,4-b]indole
SMILES COC1=CN=C(C2=C1C3=CC=CC=C3N2)C=C
Standard InChIKey HJVIUZHNRJYUTG-UHFFFAOYSA-N
Standard InChI InChI=1S/C14H12N2O/c1-3-10-14-13(12(17-2)8-15-10)9-6-4-5-7-11(9)16-14/h3-8,16H,1H2,2H3
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 Dehydrocrenatine

The barks of Ailanthus altissima (Mill.) Swingle

Biological Activity of Dehydrocrenatine

TargetsAntifection | HSP (e.g. HSP90) | TGF-β/Smad | Mdm2 | Dopamine Receptor | Caspase | NF-kB | IL Receptor

Dehydrocrenatine Dilution Calculator

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Dehydrocrenatine Molarity Calculator

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Preparing Stock Solutions of Dehydrocrenatine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.4583 mL 22.2916 mL 44.5831 mL 89.1663 mL 111.4579 mL
5 mM 0.8917 mL 4.4583 mL 8.9166 mL 17.8333 mL 22.2916 mL
10 mM 0.4458 mL 2.2292 mL 4.4583 mL 8.9166 mL 11.1458 mL
50 mM 0.0892 mL 0.4458 mL 0.8917 mL 1.7833 mL 2.2292 mL
100 mM 0.0446 mL 0.2229 mL 0.4458 mL 0.8917 mL 1.1146 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 Dehydrocrenatine

Preparative separation of alkaloids from Picrasma quassioides (D. Don) Benn. by conventional and pH-zone-refining countercurrent chromatography.[Pubmed:24968331]

Molecules. 2014 Jun 25;19(7):8752-61.

Two high-speed countercurrent chromatography (HSCCC) modes were compared by separation of major alkaloids from crude extract of Picrasma quassioides. The conventional HSCCC separation was performed with a two-phase solvent system composed of petroleum ether-ethyl acetate-methanol-water (5:5:4.5:5.5, v/v/v/v) with 200 mg loading. pH-Zone-refining CCC was performed with two-phase solvent system composed of petroleum ether-ethyl acetate-n-butanol-water (3:2:7:9, v/v/v/v) where triethylamine (10 mM) was added to the upper organic stationary phase and hydrochloric acid (5 mM) was added to the lower aqueous phase with 2 g loading. From 2 g of crude extract, 87 mg of 5-methoxycanthin-6-one (a), 38 mg of 1-methoxy-beta-carboline (b), 134 mg of 1-ethyl-4,8-dimethoxy-beta-carboline (c), 74 mg of 1-ethoxycarbonyl-beta-carboline (d), 56 mg of 1-vinyl-4,8-dimethoxy-beta-carboline (e) and 26 mg of 1-vinyl-4-dimethoxy-beta-carboline (f) were obtained with purities of over 97.0%. The results indicated that pH-zone-refining CCC is an excellent separations tool at the multigram level.

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