Evocarpine

CAS# 15266-38-3

Evocarpine

Catalog No. BCN7064----Order now to get a substantial discount!

Product Name & Size Price Stock
Evocarpine: 5mg $127 In Stock
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Quality Control of Evocarpine

Number of papers citing our products

Chemical structure

Evocarpine

3D structure

Chemical Properties of Evocarpine

Cas No. 15266-38-3 SDF Download SDF
PubChem ID 5317303 Appearance Oil
Formula C23H33NO M.Wt 339.52
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 1-methyl-2-[(Z)-tridec-8-enyl]quinolin-4-one
SMILES CCCCC=CCCCCCCCC1=CC(=O)C2=CC=CC=C2N1C
Standard InChIKey HWFYWIVOYBPLQU-SREVYHEPSA-N
Standard InChI InChI=1S/C23H33NO/c1-3-4-5-6-7-8-9-10-11-12-13-16-20-19-23(25)21-17-14-15-18-22(21)24(20)2/h6-7,14-15,17-19H,3-5,8-13,16H2,1-2H3/b7-6-
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 Evocarpine

The fruits of Evodiae fructus.

Biological Activity of Evocarpine

Description1. Evocarpine shows antimycobacterial activity. 2. Evocarpine has vasorelaxant effects, it can inhibit Ca2+ influx through voltage-dependent calcium channels.
TargetsAntifection | Calcium Channel | cAMP

Evocarpine Dilution Calculator

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Evocarpine Molarity Calculator

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Preparing Stock Solutions of Evocarpine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.9453 mL 14.7267 mL 29.4533 mL 58.9067 mL 73.6334 mL
5 mM 0.5891 mL 2.9453 mL 5.8907 mL 11.7813 mL 14.7267 mL
10 mM 0.2945 mL 1.4727 mL 2.9453 mL 5.8907 mL 7.3633 mL
50 mM 0.0589 mL 0.2945 mL 0.5891 mL 1.1781 mL 1.4727 mL
100 mM 0.0295 mL 0.1473 mL 0.2945 mL 0.5891 mL 0.7363 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 Evocarpine

The vasorelaxant effect of evocarpine in isolated aortic strips: mode of action.[Pubmed:2854068]

Eur J Pharmacol. 1988 Oct 11;155(1-2):139-43.

The effect of Evocarpine (EVO), a quinolone alkaloid isolated from Evodiae fructus, on Ca2+-blocking activity has been examined. In the isolated rat thoracic aorta Evocarpine significantly inhibited the contraction induced by 60 mM K+ with an IC50 of 9.8 microM, and that induced by external Ca2+ in the depolarized muscle in concentrations of 10-100 microM. The relaxant effect of Evocarpine and verapamil was antagonized by Bay K8644. The increase of 45Ca2+-influx induced by 60 mM K+ was significantly inhibited by 100 microM Evocarpine. In the isolated rabbit thoracic aorta 100 microM Evocarpine had no effect on the norepinephrine-induced contraction in normal medium or on the phasic contraction in Ca2+-free medium or on the transient relaxation induced by activation of the Na+ pump. The content of cyclic AMP or cyclic GMP was unchanged. These results suggest that Evocarpine inhibits Ca2+ influx through voltage-dependent calcium channels.

Antagonistic effects of indoloquinazoline alkaloids on antimycobacterial activity of evocarpine.[Pubmed:25604161]

J Appl Microbiol. 2015 Apr;118(4):864-72.

AIMS: The interaction of quinolone and indoloquinazoline alkaloids concerning their antimycobacterial activity was studied. METHODS AND RESULTS: The antimycobacterial and modulating activity of evodiamine (1), rutaecarpine (2) and Evocarpine (3) was tested on mycobacteria including three multidrug-resistant (MDR) clinical isolates of Mycobacterium tuberculosis. Antagonistic effects were concluded from fractional inhibitory concentration (FICI) values. Interaction energies of the compounds were calculated using GLUE docking module implemented in GRID. 1 and 2 exhibited weak inhibition of rapidly growing mycobacteria, however, 1 was active against Myco. tuberculosis H37Rv (MIC = 10 mg l(-1) ) while 2 was inactive. Both 1 and 2 showed a marked antagonistic effect on the susceptibility of different mycobacterial strains to 3 giving FICI values between 5 and 9. The interaction energies between compounds 1 and 2 with compound 3 suggested the possibility of complex formation in solution. CONCLUSIONS: Indoloquinazoline alkaloids markedly reduce the antimycobacterial effect of the quinolone alkaloid Evocarpine. Complex formation may play a role in the attenuation of its antimycobacterial activity. SIGNIFICANCE AND IMPACT OF THE STUDY: This study gives a striking example of antagonism between compounds present in the same plant extract which should be considered in natural product based screening projects.

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