Macusine B

CAS# 6792-07-0

Macusine B

Catalog No. BCN6471----Order now to get a substantial discount!

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Macusine B: 5mg $828 In Stock
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Quality Control of Macusine B

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Chemical structure

Macusine B

3D structure

Chemical Properties of Macusine B

Cas No. 6792-07-0 SDF Download SDF
PubChem ID 6441303 Appearance Powder
Formula C20H25N2O M.Wt 309.4
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
SMILES CC=C1C[N+]2(C3CC1C(C2CC4=C3NC5=CC=CC=C45)CO)C
Standard InChIKey KRTATNOTKFNEFT-JQERTRITSA-N
Standard InChI InChI=1S/C20H25N2O/c1-3-12-10-22(2)18-9-15-13-6-4-5-7-17(13)21-20(15)19(22)8-14(12)16(18)11-23/h3-7,14,16,18-19,21,23H,8-11H2,1-2H3/q+1/b12-3-/t14-,16+,18?,19+,22-/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 Macusine B

The herbs of Rauvolfia verticillata

Biological Activity of Macusine B

Description1. Macusine B is a dual inhibitor, has almost equal inhibitory activity on both acetylcholinesterase (AChE) and butyrylcholinesterase (BChE).
TargetsAChR | BChE

Macusine B Dilution Calculator

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Macusine B Molarity Calculator

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Preparing Stock Solutions of Macusine B

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.2321 mL 16.1603 mL 32.3206 mL 64.6412 mL 80.8016 mL
5 mM 0.6464 mL 3.2321 mL 6.4641 mL 12.9282 mL 16.1603 mL
10 mM 0.3232 mL 1.616 mL 3.2321 mL 6.4641 mL 8.0802 mL
50 mM 0.0646 mL 0.3232 mL 0.6464 mL 1.2928 mL 1.616 mL
100 mM 0.0323 mL 0.1616 mL 0.3232 mL 0.6464 mL 0.808 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 Macusine B

New Indole Alkaloids from the Bark of Rauvolfia Reflexa and their Cholinesterase Inhibitory Activity.[Pubmed:26584298]

Cell Physiol Biochem. 2015;37(5):1997-2011.

BACKGROUND/AIMS: Rauvolfia reflexa is a member of the Apocynaceae family. Plants from the Apocynaceae family have been traditionally used in the treatment of age-related brain disorders Methods and Results: Two new indole alkaloids, rauvolfine C (1) and 3-methyl-10,11-dimethoxy-6-methoxycarbonyl-beta-carboline (2), along with five known, Macusine B (3), vinorine (4), undulifoline (5), isoresrpiline (6) and rescinnamine (7) were isolated from the bark of Rauvolfia reflexa. Cholinesterase inhibitory assay and molecular docking were performed to get insight of the inhibitory activity and molecular interactions of the compounds. The compounds showed good to moderate cholinesterase inhibitory activity with IC50 values in the range of 8.06 to 73.23 microM. Compound 7 was found to be the most potent inhibitor of both acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). Compounds 1, 2, 5 and 6 were found to be selective towards BChE, while compounds 3, 4 and 7 were dual inhibitors, having almost equal inhibitory activity on both AChE and BChE. Molecular docking revealed that compounds 6 and 7 interacted differently on AChE and BChE, by means of hydrophobic interactions and hydrogen bonding. In AChE, the indole moiety of both compounds interacted with the residues lining the peripheral anionic site, whereas in BChE, their methoxy groups are primarily responsible for the strong inhibitory activity via interactions with residues at the active site of the enzyme. CONCLUSION: Two new and five known indole alkaloids were isolated from R. reflexa. Among the compounds, 7 and 6 showed the most potent and promising cholinesterase inhibitory activity, worthy for further investigations.

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