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Dehydrobruceantin

CAS# 53662-98-9

Dehydrobruceantin

Catalog No. BCN7617----Order now to get a substantial discount!

Product Name & Size Price Stock
Dehydrobruceantin: 5mg $1150 In Stock
Dehydrobruceantin: 10mg Please Inquire In Stock
Dehydrobruceantin: 20mg Please Inquire Please Inquire
Dehydrobruceantin: 50mg Please Inquire Please Inquire
Dehydrobruceantin: 100mg Please Inquire Please Inquire
Dehydrobruceantin: 200mg Please Inquire Please Inquire
Dehydrobruceantin: 500mg Please Inquire Please Inquire
Dehydrobruceantin: 1000mg Please Inquire Please Inquire

Quality Control of Dehydrobruceantin

Number of papers citing our products

Chemical structure

Dehydrobruceantin

3D structure

Chemical Properties of Dehydrobruceantin

Cas No. 53662-98-9 SDF Download SDF
PubChem ID 15330899 Appearance Powder
Formula C28H34O11 M.Wt 546.56
Type of Compound Diterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name methyl (1R,2S,3R,6R,13S,14R,15R,16S,17S)-3-[(E)-3,4-dimethylpent-2-enoyl]oxy-11,15,16-trihydroxy-9,13-dimethyl-4,10-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadeca-8,11-diene-17-carboxylate
SMILES CC1=C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C(C)C)(C(C(C5C2(C=C(C1=O)O)C)O)O)C(=O)OC
Standard InChIKey ZLLWLVCJZCJECL-AOXBTAHBSA-N
Standard InChI InChI=1S/C28H34O11/c1-11(2)12(3)7-17(30)39-20-22-27-10-37-28(22,25(35)36-6)23(33)19(32)21(27)26(5)9-15(29)18(31)13(4)14(26)8-16(27)38-24(20)34/h7,9,11,16,19-23,29,32-33H,8,10H2,1-6H3/b12-7+/t16-,19-,20-,21-,22-,23+,26+,27-,28+/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 Dehydrobruceantin

The seeds of Brucea javanica (L.) Merr.

Biological Activity of Dehydrobruceantin

Description1. Dehydrobruceantin has anti-tuberculosis activity.
TargetsAntifection

Dehydrobruceantin Dilution Calculator

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Dehydrobruceantin Molarity Calculator

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Preparing Stock Solutions of Dehydrobruceantin

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.8296 mL 9.1481 mL 18.2963 mL 36.5925 mL 45.7406 mL
5 mM 0.3659 mL 1.8296 mL 3.6593 mL 7.3185 mL 9.1481 mL
10 mM 0.183 mL 0.9148 mL 1.8296 mL 3.6593 mL 4.5741 mL
50 mM 0.0366 mL 0.183 mL 0.3659 mL 0.7319 mL 0.9148 mL
100 mM 0.0183 mL 0.0915 mL 0.183 mL 0.3659 mL 0.4574 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 Dehydrobruceantin

Anti-tuberculosis activity of quassinoids.[Pubmed:9332005]

Chem Pharm Bull (Tokyo). 1997 Sep;45(9):1527-9.

In vitro evaluation of anti-tuberculosis activity was conducted for fifty-six quassinoids isolated in our laboratory from Simaroubaceous plants, Ailanthus altissima (= Aa, 10 compounds), Brucea antidysenterica (= Ba, 16 compounds), Picrasma ailanthoides (= Pa, 14 compounds), and Brucea javanica (= Bj, 16 compounds). Of the compounds tested, shinjulactone K (1), ailanthone (2), shinjudilactone (3), and Dehydrobruceantin (4) were the most potent. Although the activities were very low (0-19%), the resulting data provided a picture of structure-activity relationships.

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