Scutebata G

CAS# 1207181-63-2

Scutebata G

2D Structure

Catalog No. BCN6101----Order now to get a substantial discount!

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Scutebata G: 5mg $1012 In Stock
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Quality Control of Scutebata G

3D structure

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Scutebata G

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Chemical Properties of Scutebata G

Cas No. 1207181-63-2 SDF Download SDF
PubChem ID 46183619 Appearance Powder
Formula C40H41NO9 M.Wt 679.8
Type of Compound Diterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name [(3S,4aR,5S,6R,6aR,10R,10aS,10bR)-5,10-dibenzoyloxy-4a,6a,7,10b-tetramethyl-2'-oxospiro[2,5,6,9,10,10a-hexahydro-1H-benzo[f]chromene-3,4'-oxolane]-6-yl] pyridine-3-carboxylate
SMILES CC1=CCC(C2C1(C(C(C3(C2(CCC4(O3)CC(=O)OC4)C)C)OC(=O)C5=CC=CC=C5)OC(=O)C6=CN=CC=C6)C)OC(=O)C7=CC=CC=C7
Standard InChIKey GREIZWACRDERNJ-RXCLYVCLSA-N
Standard InChI InChI=1S/C40H41NO9/c1-25-17-18-29(47-34(43)26-12-7-5-8-13-26)31-37(2)19-20-40(22-30(42)46-24-40)50-39(37,4)33(49-35(44)27-14-9-6-10-15-27)32(38(25,31)3)48-36(45)28-16-11-21-41-23-28/h5-17,21,23,29,31-33H,18-20,22,24H2,1-4H3/t29-,31-,32+,33+,37-,38+,39+,40+/m1/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 Scutebata G

The herbs of Scutellaria barbata D.Don

Biological Activity of Scutebata G

In vitro

Cytotoxic neoclerodane diterpenoids from Scutellaria barbata.[Pubmed: 20078074]

J Nat Prod. 2010 Feb 26;73(2):233-6.

Seven new neoclerodane diterpenoids, scutebata A-Scutebata G (1-7), have been isolated from Scutellaria barbata.
METHODS AND RESULTS:
Compounds 1-3 possess a rare alpha-hydroxy group in their alpha,beta-unsaturated lactone rings. Their structures were elucidated by spectroscopic analysis, and the relative configuration of scutebata A was deduced using ROESY data and the computational DFT method. Compounds 1, 2, 4, 5, and 6 were evaluated for in vitro cytotoxicity against six human cancer cell lines: HL-60, SMMC-7721, A-549, SK-BR-3, CACO-2, and PANC-1.
CONCLUSIONS:
Scutebata A (1) showed weak cytotoxicity against SK-BR-3 with an IC(50) value of 15.2 muM.

Scutebata G Dilution Calculator

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Scutebata G Molarity Calculator

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Preparing Stock Solutions of Scutebata G

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.471 mL 7.3551 mL 14.7102 mL 29.4204 mL 36.7755 mL
5 mM 0.2942 mL 1.471 mL 2.942 mL 5.8841 mL 7.3551 mL
10 mM 0.1471 mL 0.7355 mL 1.471 mL 2.942 mL 3.6776 mL
50 mM 0.0294 mL 0.1471 mL 0.2942 mL 0.5884 mL 0.7355 mL
100 mM 0.0147 mL 0.0736 mL 0.1471 mL 0.2942 mL 0.3678 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 Scutebata G

Cytotoxic neoclerodane diterpenoids from Scutellaria barbata.[Pubmed:20078074]

J Nat Prod. 2010 Feb 26;73(2):233-6.

Seven new neoclerodane diterpenoids, scutebatas A-G (1-7), have been isolated from Scutellaria barbata. Compounds 1-3 possess a rare alpha-hydroxy group in their alpha,beta-unsaturated lactone rings. Their structures were elucidated by spectroscopic analysis, and the relative configuration of scutebata A was deduced using ROESY data and the computational DFT method. Compounds 1, 2, 4, 5, and 6 were evaluated for in vitro cytotoxicity against six human cancer cell lines: HL-60, SMMC-7721, A-549, SK-BR-3, CACO-2, and PANC-1. Scutebata A (1) showed weak cytotoxicity against SK-BR-3 with an IC(50) value of 15.2 muM.

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