Murrayamine E

CAS# 172617-68-4

Murrayamine E

Catalog No. BCN7908----Order now to get a substantial discount!

Product Name & Size Price Stock
Murrayamine E:5mg Please Inquire In Stock
Murrayamine E:10mg Please Inquire In Stock
Murrayamine E:20mg Please Inquire In Stock
Murrayamine E:50mg Please Inquire In Stock

Quality Control of Murrayamine E

Number of papers citing our products

Chemical structure

Murrayamine E

3D structure

Chemical Properties of Murrayamine E

Cas No. 172617-68-4 SDF Download SDF
PubChem ID 15768256 Appearance Powder
Formula C23H25NO2 M.Wt 347.45
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (14S,17R,19R)-3,13,13,17-tetramethyl-21-oxa-12-azahexacyclo[10.7.1.12,17.05,20.06,11.014,19]henicosa-1(20),2,4,6(11),7,9-hexaen-9-ol
SMILES CC1=C2C3=C4C(=C1)C5=C(N4C(C6C3CC(O2)(CC6)C)(C)C)C=C(C=C5)O
Standard InChIKey YDUWCKHQORLZSO-SAHWJRBASA-N
Standard InChI InChI=1S/C23H25NO2/c1-12-9-15-14-6-5-13(25)10-18(14)24-20(15)19-16-11-23(4,26-21(12)19)8-7-17(16)22(24,2)3/h5-6,9-10,16-17,25H,7-8,11H2,1-4H3/t16-,17+,23-/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 Murrayamine E

The herbs of Murraya exotica

Biological Activity of Murrayamine E

DescriptionMurrayamine E is a natural product from Murraya exotica.

Protocol of Murrayamine E

Structure Identification
J Org Chem. 2015 Jun 5;80(11):5666-73.

Total syntheses of murrayamine E, I, and K.[Pubmed: 25915067 ]

We describe efficient synthetic routes to murrayamine A (mukoenine C), O-methylmurrayamine A, mahanine, O-methylmahanine, and murrayamine D and the first total syntheses of Murrayamine E, I, and K. Key steps are a palladium-catalyzed construction of the carbazole framework and an annulation of the pyran ring, which is either catalyzed by phenylboronic acid or promoted by a Lewis acid.

Murrayamine E Dilution Calculator

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Murrayamine E Molarity Calculator

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Preparing Stock Solutions of Murrayamine E

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.8781 mL 14.3906 mL 28.7811 mL 57.5622 mL 71.9528 mL
5 mM 0.5756 mL 2.8781 mL 5.7562 mL 11.5124 mL 14.3906 mL
10 mM 0.2878 mL 1.4391 mL 2.8781 mL 5.7562 mL 7.1953 mL
50 mM 0.0576 mL 0.2878 mL 0.5756 mL 1.1512 mL 1.4391 mL
100 mM 0.0288 mL 0.1439 mL 0.2878 mL 0.5756 mL 0.7195 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 Murrayamine E

Total syntheses of murrayamine E, I, and K.[Pubmed:25915067]

J Org Chem. 2015 Jun 5;80(11):5666-73.

We describe efficient synthetic routes to murrayamine A (mukoenine C), O-methylmurrayamine A, mahanine, O-methylmahanine, and murrayamine D and the first total syntheses of Murrayamine E, I, and K. Key steps are a palladium-catalyzed construction of the carbazole framework and an annulation of the pyran ring, which is either catalyzed by phenylboronic acid or promoted by a Lewis acid.

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