Home >> Research Area >>Natural Products>>Diterpenoids>> 7,13-Dideacetyl-9,10-didebenzoyltaxchinin C

7,13-Dideacetyl-9,10-didebenzoyltaxchinin C

CAS# 156497-25-5

7,13-Dideacetyl-9,10-didebenzoyltaxchinin C

Catalog No. BCN7670----Order now to get a substantial discount!

Product Name & Size Price Stock
7,13-Dideacetyl-9,10-didebenzoyltaxchinin C:5mg Please Inquire In Stock
7,13-Dideacetyl-9,10-didebenzoyltaxchinin C:10mg Please Inquire In Stock
7,13-Dideacetyl-9,10-didebenzoyltaxchinin C:20mg Please Inquire In Stock
7,13-Dideacetyl-9,10-didebenzoyltaxchinin C:50mg Please Inquire In Stock

Quality Control of 7,13-Dideacetyl-9,10-didebenzoyltaxchinin C

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Chemical structure

7,13-Dideacetyl-9,10-didebenzoyltaxchinin C

3D structure

Chemical Properties of 7,13-Dideacetyl-9,10-didebenzoyltaxchinin C

Cas No. 156497-25-5 SDF Download SDF
PubChem ID 101670843 Appearance Powder
Formula C29H38O10 M.Wt 546.60
Type of Compound Diterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
SMILES CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C5=CC=CC=C5)(CO4)OC(=O)C)O)C)O)O
Standard InChIKey ULZWCGMUIFQZOD-KIDMXVSKSA-N
Standard InChI InChI=1S/C29H38O10/c1-14-17(31)12-28(26(3,4)36)20(14)21(33)23(34)27(5)18(32)11-19-29(13-37-19,39-15(2)30)22(27)24(28)38-25(35)16-9-7-6-8-10-16/h6-10,17-19,21-24,31-34,36H,11-13H2,1-5H3/t17-,18-,19+,21+,22-,23-,24-,27+,28-,29-/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.
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 7,13-Dideacetyl-9,10-didebenzoyltaxchinin C

The whole plants of Taxus chinensis var. mairei.

Biological Activity of 7,13-Dideacetyl-9,10-didebenzoyltaxchinin C

Description7,13-Dideacetyl-9,10-didebenzoyltaxchinin C is a natural product from Taxus chinensis var. mairei.

Protocol of 7,13-Dideacetyl-9,10-didebenzoyltaxchinin C

Structure Identification
Chinese Journal of Natural Medicines, 2006, 4(1):52-57.

Chemical constituents of cultured Taxus mairei (I)[Reference: WebLink]

To intensively investigate the chemical constituents of cultured (3y) Taxus chinensis var. mairei (Lemee et Levl).
METHODS AND RESULTS:
The whole plant was extracted with ethanol, the ethanol extract was subjected to extraction with methylene trichloride, which was submitted to chromatography on silica gel and Sephadex column to isolate some compounds. And their structures were elucidated on the basis of spectral analysis (UV, IR, ESI-MS, 1H NMR, 13C NMR). The compounds were identified as 2α-deacetoxytaxinine J (I), taxuyunnanine C (II), yunnanxane (III), taxinine J(IV), 1-dehydroxy-baccatin VI (V), taxol (VI), 19-debenzoyl-19-acetyltaxinine M (VII), taxinine M (VIII), taxicin (IX), taxa-4(20)-11-diene-2α, 5α, 10β-triacetoxy-14β, 2-methybutyrate (X), baccatin III (XI), cephalomannine(XII), 7,13-Dideacetyl-9,10-didebenzoyltaxchinin C (XIII), taxamairin A(XIV), taxamairin B (XV), α-conidendrin (XVI), secoisolariciresinol (XVII), isotaxiresinol (XVIII), β-sitosterol (XIX) and daucosterol (XX), VII, XIII were isolated from this source for the first time.
CONCLUSIONS:
The chemical constituents of planted Taxus mairei are nearly the same as that of the wild.

7,13-Dideacetyl-9,10-didebenzoyltaxchinin C Dilution Calculator

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7,13-Dideacetyl-9,10-didebenzoyltaxchinin C Molarity Calculator

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Preparing Stock Solutions of 7,13-Dideacetyl-9,10-didebenzoyltaxchinin C

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.8295 mL 9.1475 mL 18.2949 mL 36.5898 mL 45.7373 mL
5 mM 0.3659 mL 1.8295 mL 3.659 mL 7.318 mL 9.1475 mL
10 mM 0.1829 mL 0.9147 mL 1.8295 mL 3.659 mL 4.5737 mL
50 mM 0.0366 mL 0.1829 mL 0.3659 mL 0.7318 mL 0.9147 mL
100 mM 0.0183 mL 0.0915 mL 0.1829 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 7,13-Dideacetyl-9,10-didebenzoyltaxchinin C

Chemical constituents of cultured Taxus mairei (I)

Chinese Journal of Natural Medicines, 2006, 4(1):52-57.

To intensively investigate the chemical constituents of cultured (3y) Taxus chinensis var. mairei (Lemee et Levl). Methods: The whole plant was extracted with ethanol, the ethanol extract was subjected to extraction with methylene trichloride, which was submitted to chromatography on silica gel and Sephadex column to isolate some compounds. And their structures were elucidated on the basis of spectral analysis (UV, IR, ESI-MS, 1H NMR, 13C NMR). Results: The compounds were identified as 2α-deacetoxytaxinine J (I), taxuyunnanine C (II), yunnanxane (III), taxinine J(IV), 1-dehydroxy-baccatin VI (V), taxol (VI), 19-debenzoyl-19-acetyltaxinine M (VII), taxinine M (VIII), taxicin (IX), taxa-4(20)-11-diene-2α, 5α, 10β-triacetoxy-14β, 2-methybutyrate (X), baccatin III (XI), cephalomannine(XII), 7,13-Dideacetyl-9,10-didebenzoyltaxchinin C (XIII), taxamairin A(XIV), taxamairin B (XV), α-conidendrin (XVI), secoisolariciresinol (XVII), isotaxiresinol (XVIII), β-sitosterol (XIX) and daucosterol (XX), VII, XIII were isolated from this source for the first time. Conclusion: The chemical constituents of planted Taxus mairei are nearly the same as that of the wild.

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