BruceantinolCAS# 53729-52-5 |
Quality Control & MSDS
3D structure
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Number of papers citing our products
| Cas No. | 53729-52-5 | SDF | Download SDF |
| PubChem ID | 5281305 | Appearance | Powder |
| Formula | C30H38O13 | M.Wt | 606.62 |
| Type of Compound | Diterpenoids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| SMILES | CC1=C(C(=O)CC2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC(=O)C=C(C)C(C)(C)OC(=O)C)(OC5)C(=O)OC)O)O)C)O | ||
| Standard InChIKey | SREUSBYRKOPNJK-AJPRWBMOSA-N | ||
| Standard InChI | InChI=1S/C30H38O13/c1-12(27(4,5)43-14(3)31)8-18(33)42-21-23-29-11-40-30(23,26(38)39-7)24(36)20(35)22(29)28(6)10-16(32)19(34)13(2)15(28)9-17(29)41-25(21)37/h8,15,17,20-24,34-36H,9-11H2,1-7H3/b12-8+/t15-,17+,20+,21+,22+,23+,24-,28-,29+,30-/m0/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. |
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| 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. |
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| 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. | ||
| Description | 1. Bruceantinol has antiviral activity, it can inhibit pepper mottle virus in pepper. 2. Bruceantinol shows in vitro inhibitory activity against Trypanosoma evansi. 3. Bruceantinol shows antibabesial activity against Babesia gibsoni in vitro, with the IC50 value of 12 ng/mL. |
| Targets | Antifection |
Bruceantinol Dilution Calculator
Bruceantinol Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 1.6485 mL | 8.2424 mL | 16.4848 mL | 32.9696 mL | 41.212 mL |
| 5 mM | 0.3297 mL | 1.6485 mL | 3.297 mL | 6.5939 mL | 8.2424 mL |
| 10 mM | 0.1648 mL | 0.8242 mL | 1.6485 mL | 3.297 mL | 4.1212 mL |
| 50 mM | 0.033 mL | 0.1648 mL | 0.3297 mL | 0.6594 mL | 0.8242 mL |
| 100 mM | 0.0165 mL | 0.0824 mL | 0.1648 mL | 0.3297 mL | 0.4121 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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Screening of Indonesian medicinal plant extracts for antibabesial activity and isolation of new quassinoids from Brucea javanica.[Pubmed:17896817]
J Nat Prod. 2007 Oct;70(10):1654-7.
Boiled extracts derived from 28 Indonesian medicinal plants were screened for their antibabesial activity against Babesia gibsoni in vitro. Of these extracts, the fruit of Brucea javanica was the most active in inhibiting parasite growth at a concentration of 10 microg/mL. Bioassay-guided fractionation of the fruit extract of Br. javanica led to the isolation of two new quassinoids, Bruceantinol B and bruceine J, and the structures of these compounds were elucidated on the basis of their spectroscopic data and by chemical transformation to known compounds. In addition, the known quassinoids bruceines A-D, Bruceantinol, and yadanziolide A were isolated. Antibabesial activities were also examined in vitro, and bruceine A and Bruceantinol were shown to be more potent than diminazene aceturate, a drug (IC50 = 103 ng/mL) used clinically against B. gibsoni, with IC50 values of 4 and 12 ng/mL, respectively.
Antitrypanosomal activities of acetylated bruceines A and C; a structure-activity relationship study.[Pubmed:21822605]
J Nat Med. 2012 Jan;66(1):233-40.
The crude extract of Brucea javanica showed strong in vitro inhibitory activity against Trypanosoma evansi. Among the isolated quassinoids, bruceines A, C, and Bruceantinol were found to be the most potent compounds against T. evansi. To gain a deeper understanding of the relationship between the free hydroxyl groups and the activity, several O-acetylated derivatives of bruceines A and C were synthesized and their in vitro antitrypanosomal activities against trypomastigotes of T. evansi were examined and compared with those of the original compounds. The following structure-activity relationships were observed: (1) the free hydroxyl groups at positions C-3, C-11, and C-12 are essential for antitrypanosomal activity; (2) the C-11 and C-12 hydroxyl groups are more important for the activity than the enolic hydroxyl group at C-3, and; (3) the free hydroxyl group at C-4' of bruceine C does not have any significant effect on the activity.
Quassinoids isolated from Brucea javanica inhibit pepper mottle virus in pepper.[Pubmed:27686478]
Virus Res. 2017 Jan 2;227:49-56.
A green fluorescent protein (GFP)-tagged pepper mottle virus (PepMoV) based leaf-disc method and systemic host method were developed to identify antiviral agents. Preliminary experiments using a PepMoV-GFP based leaf-disc method led to the isolation of five quassinoids, including brusatol (1), bruceantin (2), brucein A (3), Bruceantinol (4), and brucein B (5), from the CH3OH extract of Brucea javanica. All isolated compounds exhibited inactivation effects in systemic host plants, and compounds 3 and 4 were potent, with a minimum inhibitory concentration of 10muM. Furthermore, compound 3 was found to have a protective effect at the tested concentration of 40muM.
