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13-O-Deacetyltaxumairol Z

13-O-Deacetyltaxumairol Z

Catalog No. BCN4945
Size Price Stock
20mg $298 In stock
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Quality Control of 13-O-Deacetyltaxumairol Z

Chemical structure

13-O-Deacetyltaxumairol Z

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Chemical Properties of 13-O-Deacetyltaxumairol Z

Cas No. 220935-39-7 SDF Download SDF
SMILES O=C(O[C@H]4[C@H]1[C@]([C@@H](O)C[C@H]2OC[C@@]12OC(=O)C)(COC(=O)C)[C@@H](O)[C@H](O)/C3=C(C)[C@@H](O)C[C@]34C(O)(C)C)c5ccccc5
Standard InChI InChI=1S/C31H40O12/c1-15-19(34)12-30(28(4,5)39)22(15)23(36)25(37)29(13-40-16(2)32)20(35)11-21-31(14-41-21,43-17(3)33)24(29)26(30)42-27(38)18-9-7-6-8-10-18/h6-10,19-21,23-26,34-37,39H,11-14H2,1-5H3/t19-,20-,21+,23+,24-,25-,26-,29+,30-,31-/m0/s1
Type of Compound Diterpenoids Appearance Powder
Formula C31H40O12 M.Wt 604.7
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
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.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other courier with RT , or blue ice upon request.

Preparing Stock Solutions of 13-O-Deacetyltaxumairol Z

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.6537 mL 8.2686 mL 16.5371 mL 33.0743 mL 41.3428 mL
5 mM 0.3307 mL 1.6537 mL 3.3074 mL 6.6149 mL 8.2686 mL
10 mM 0.1654 mL 0.8269 mL 1.6537 mL 3.3074 mL 4.1343 mL
50 mM 0.0331 mL 0.1654 mL 0.3307 mL 0.6615 mL 0.8269 mL
100 mM 0.0165 mL 0.0827 mL 0.1654 mL 0.3307 mL 0.4134 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.

Preparation of 13-O-Deacetyltaxumairol Z

This product is isolated and purified from the barks of Taxus chinensis

References on 13-O-Deacetyltaxumairol Z

Taxumairols X--Z, new taxoids from Taiwanese Taxus mairei.[Pubmed: 12499590]

In addition to 19-dydroxybaccatin III, 1beta-hydroxy-5 alpha-deacetylbaccatin I, taxayuntin G and 13-O-Deacetyltaxumairol Z (4), three new taxane diterpenoids, taxumairols X (1), Y (2), Z (3) have been isolated from extracts of the Formosan Taxus mairei (LEMEE & LEVL.) S. Y. HU. Compounds 1-2 belong to the 11(15-->1)-abeo-taxane system, having a tetrahydrofuran ring at C-2, C-3, C-4 and C-20. The new compound 3 and 4, which was misidentified previously are derivatives of 11(15-->1)-abeo-taxane with an intact oxirane system. The structures of compounds 1-4 were elucidated on the basis of extensive two dimensional (2D)-NMR analysis.


13-O-Deacetyltaxumairol Z ,220935-39-7,Nature Products, supplier, inhibitor,Antagonist,Blocker,Modulator,Agonist, activators, activates, potent, BioCrick

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