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|Size /Price /Stock
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More articles cited ChemFaces products.
Eur J Pharmacol.2018, 832:96-103J Ethnopharmacol.2017, 206:73-77J Sep Sci.2018, 41(7):1682-1690Exp Neurobiol.2018, 27(3):200-209Current Traditional Medicine, ...2021...Int J Mol Sci.2020, 21(8):2790.J Adv Res.2021, 35:245-257. J Liq Chromatogr R T...2018...
Phytomedicine.2016, 23(4):331-9Molecules.2020, 25(21):5091.Molecular & Cellular Toxicology...2022...Advances in Traditional Medicine ...2021...Eur Rev Med Pharmacol Sci....2020...United States Patent Application...2020...J. Food Composition and Anal....2022...Korean Herb. Med. Inf....2020...
Daru.2022, 30(2):273-288.Pharmaceuticals (Basel)....2021...Biomedicines.2021, 9(8):996.J of l. Chroma.&Related Tech...2020...J Agric Food Chem.2015, 63(44):9869-78Sci. Rep.2015, 14-23Analytical methods2019, 11(6)
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Anal Bioanal Chem.2020, 412(12):3005-3015.J Nat Med.2021, doi: 10.1007.Antioxidants (Basel).2020, 9(6):544. Sci Rep.2019, 9:12132Arch Toxicol.2017, 91(10):3225-3245Metabolites.2020, 10(12):497.J of l. Chroma.&Related Tech2020, 43(11-12):414-423.Biofactors.2018, 44(2):168-179Cardiovasc Toxicol.2019, 19(4):297-305J of the Korean Society of Cosmetics and Cosmetology2018, 399-406
Related Screening Libraries
|| Taccalonolide A is the first microtubule stabilizing agent to be discovered from a plant
since identification of the mechanism of action of paclitaxel and it is the first natural product steroid identified to have these cellular effects.
||Bcl-2/Bax | Caspase | P-gp|
Taccalonolide A Description
||The rhizomes of Schizocapsa plantaginea Hance
||Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
||Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please email to: firstname.lastname@example.org
||The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
ChemFaces New Products and Compounds
Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals
Cell. 2018 Jan 11;172(1-2):249-261.e12. doi: 10.1016/j.cell.2017.12.019.IF=36.216(2019)PMID: 29328914
Cell Metab. 2020 Mar 3;31(3):534-548.e5. doi: 10.1016/j.cmet.2020.01.002.IF=22.415(2019)PMID: 32004475
Mol Cell. 2017 Nov 16;68(4):673-685.e6. doi: 10.1016/j.molcel.2017.10.022.IF=14.548(2019)PMID: 29149595
ACS Nano. 2018 Apr 24;12(4): 3385-3396. doi: 10.1021/acsnano.7b08969.IF=13.903(2019)PMID: 29553709
Nature Plants. 2016 Dec 22;3: 16206. doi: 10.1038/nplants.2016.205.IF=13.297(2019)PMID: 28005066
Sci Adv. 2018 Oct 24;4(10): eaat6994. doi: 10.1126/sciadv.aat6994.IF=12.804(2019)PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
|April 12, 2005 |
|Taccalonolide microtubule stabilizing agents[Reference: WebLink]|
|In accordance with the present invention, there have been identified extracts from a tropical plant that initiate paclitaxel-like microtubule bundling. |
METHODS AND RESULTS:
Bioassay-directed purification yields the steroid Taccalonolide A. Taccalonolide, like paclitaxel, initiates the formation of abnormal interphaes and mitotic microtubules. Cells treated with taccalonolide exhibit thick bundles of microtubules that appear to nucleate independent of the microtubule organizing center. Abnormal mitotic spindles consisting of multi-polar spindles are initiated by Taccalonolide And resemble abnormal mitotic spindles found in the presence of paclitaxel. Like paclitaxel, taccalonolide causes the breakdown of the nucleus into micronuclei. Taccalonolide causes G2/M arrest, Bc1-2 phosphorylation and initiates an apoptotic cascade that includes the activation of caspase 3. Taccalonolide is an effective inhibitor of proliferation against both SK-OV-3 and MDA-MB-435 cell with IC50 values of 2.3 μM and 2.1 μM respectively. In contrast to paclitaxel, taccalonolide is effective against the multidrug resistant SKVLB-1 cellline and thus appears to be a poor substrate for P-glycoprotein-mediated transport. Although taccalonolide is almost equipotent with paclitaxel in its effects on cellular microtubules, it is much less potent than paclitaxel in its ability to initiate the polymerization of purified tubulin and microtubule protein.
Taccalonolide A is the first microtubule stabilizing agent to be discovered from a plant since identification of the mechanism of action of paclitaxel and it is the first natural product steroid identified to have these cellular effects.
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