Borapetoside F

CAS# 151200-50-9

Borapetoside F

Catalog No. BCN6413----Order now to get a substantial discount!

Product Name & Size Price Stock
Borapetoside F: 5mg $989 In Stock
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Quality Control of Borapetoside F

Number of papers citing our products

Chemical structure

Borapetoside F

3D structure

Chemical Properties of Borapetoside F

Cas No. 151200-50-9 SDF Download SDF
PubChem ID 73812792 Appearance Powder
Formula C27H34O11 M.Wt 534.6
Type of Compound Diterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name methyl 2-(furan-3-yl)-6a,10b-dimethyl-4-oxo-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,6,9,10,10a-hexahydrobenzo[f]isochromene-7-carboxylate
SMILES CC12CC(OC(=O)C1=CC(C3(C2CCC=C3C(=O)OC)C)OC4C(C(C(C(O4)CO)O)O)O)C5=COC=C5
Standard InChIKey UQBSOXXWYBLSSJ-UHFFFAOYSA-N
Standard InChI InChI=1S/C27H34O11/c1-26-10-16(13-7-8-35-12-13)36-24(33)15(26)9-19(27(2)14(23(32)34-3)5-4-6-18(26)27)38-25-22(31)21(30)20(29)17(11-28)37-25/h5,7-9,12,16-22,25,28-31H,4,6,10-11H2,1-3H3
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 Borapetoside F

The stems of Tinospora tuberculata Beumée.

Biological Activity of Borapetoside F

DescriptionStandard reference

Protocol of Borapetoside F

Structure Identification
European Journal of Organic Chemistry,1993,1993(5):491-5.

Studies on the Constituents of the Stems of Tinospora tuberculata, IV. Isolation and Structure Elucidation of the Five New Furanoid Diterpene Glycosides Borapetoside C–G[Reference: WebLink]


METHODS AND RESULTS:
Five new furanoid diterpene glycosides, named borapetoside C (1),borapetoside D (2),borapetoside E (3),Borapetoside F (4), and borapetoside G (5), were isolated from the stems of Tinospora tuberculata Beumée (Menispermaceae). The structures of 1–5 were elucidated by chemical and spectroscopic methods.

Borapetoside F Dilution Calculator

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Borapetoside F Molarity Calculator

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Preparing Stock Solutions of Borapetoside F

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.8706 mL 9.3528 mL 18.7056 mL 37.4111 mL 46.7639 mL
5 mM 0.3741 mL 1.8706 mL 3.7411 mL 7.4822 mL 9.3528 mL
10 mM 0.1871 mL 0.9353 mL 1.8706 mL 3.7411 mL 4.6764 mL
50 mM 0.0374 mL 0.1871 mL 0.3741 mL 0.7482 mL 0.9353 mL
100 mM 0.0187 mL 0.0935 mL 0.1871 mL 0.3741 mL 0.4676 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 Borapetoside F

Antioxidant and lipophilic constituents of Tinospora crispa.[Pubmed:17253260]

Planta Med. 1998 Jun;64(5):393-6.

TLC autographic assays revealed in the CH(2)Cl(2) extract of Tinospora crispa Miers (Menispermaceae) the presence of three compounds exhibiting antioxidant and radical scavenging properties towards beta-carotene and 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical. They were isolated and identified as N-CIS-feruloyltyramine, N-trans-feruloyltyramine and secoisolariciresinol. When tested in dilution assays on the reduction of the DPPH radical, these 3 compounds proved to be more active than the synthetic antioxidant butylhydroxytoluene (BHT). Further investigation of the CH(2)Cl(2) extract led to the isolation of vanillin, syringin, the alkaloid N-formylnornuciferin and the diterpene derivatives borapetosides B and C. In addition, a LC/UV/MS analysis enabled the on-line identification of Borapetoside F and N-formylannonain.

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