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Kadsuracoccinic acid A

CAS# 1016260-22-2

Kadsuracoccinic acid A

Catalog No. BCN5829----Order now to get a substantial discount!

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Kadsuracoccinic acid A:5mg Please Inquire In Stock
Kadsuracoccinic acid A:10mg Please Inquire In Stock
Kadsuracoccinic acid A:20mg Please Inquire In Stock
Kadsuracoccinic acid A:50mg Please Inquire In Stock

Quality Control of Kadsuracoccinic acid A

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Chemical structure

Kadsuracoccinic acid A

3D structure

Chemical Properties of Kadsuracoccinic acid A

Cas No. 1016260-22-2 SDF Download SDF
PubChem ID 24850148 Appearance Powder
Formula C30H44O4 M.Wt 468.7
Type of Compound Triterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (Z,6Z)-6-[(3aS,6S,7S,9aS,9bS)-6-(2-carboxyethyl)-3a,6,9b-trimethyl-7-prop-1-en-2-yl-2,4,7,8,9,9a-hexahydro-1H-cyclopenta[a]naphthalen-3-ylidene]-2-methylhept-2-enoic acid
SMILES CC(=C)C1CCC2C(=CCC3(C2(CCC3=C(C)CCC=C(C)C(=O)O)C)C)C1(C)CCC(=O)O
Standard InChIKey QOIBKZDJHBYYMX-AVNVPESYSA-N
Standard InChI InChI=1S/C30H44O4/c1-19(2)22-11-12-25-24(28(22,5)16-15-26(31)32)14-18-29(6)23(13-17-30(25,29)7)20(3)9-8-10-21(4)27(33)34/h10,14,22,25H,1,8-9,11-13,15-18H2,2-7H3,(H,31,32)(H,33,34)/b21-10-,23-20-/t22-,25+,28-,29+,30-/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 Kadsuracoccinic acid A

The herb of Kadsura coccinea

Biological Activity of Kadsuracoccinic acid A

Description1. Kadsuracoccinic acid A has anticancer activity. 2. Kadsuracoccinic acid A induces significant cleavage arrest. 3. Kadsuracoccinic acid A may be related to the preservation of the progression of the M phase.

Kadsuracoccinic acid A Dilution Calculator

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Kadsuracoccinic acid A Molarity Calculator

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Preparing Stock Solutions of Kadsuracoccinic acid A

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.1336 mL 10.6678 mL 21.3356 mL 42.6712 mL 53.339 mL
5 mM 0.4267 mL 2.1336 mL 4.2671 mL 8.5342 mL 10.6678 mL
10 mM 0.2134 mL 1.0668 mL 2.1336 mL 4.2671 mL 5.3339 mL
50 mM 0.0427 mL 0.2134 mL 0.4267 mL 0.8534 mL 1.0668 mL
100 mM 0.0213 mL 0.1067 mL 0.2134 mL 0.4267 mL 0.5334 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 Kadsuracoccinic acid A

Kadsuracoccinic acids A-C, ring-A seco-lanostane triterpenes from Kadsura coccinea and their effects on embryonic cell division of Xenopus laevis.[Pubmed:18271558]

J Nat Prod. 2008 Apr;71(4):739-41.

Three new 3,4- seco-lanostanes, kadsuracoccinic acids A-C ( 1- 3), were isolated from the medicinal plant Kadsura coccinea, in addition to the known compounds kadsuric acid ( 4) and micranoic acid A ( 5). The structures of 1- 3 were elucidated by analysis of their 2D-NMR spectroscopic data. Furthermore, the relative conformation of 1 was confirmed by an X-ray crystallographic study. This is the first report of a 3,4- seco-lanostane-type triterpene with a 17(20)-ene functional group. Treatment of cultured individual Xenopus laevis cells with 1 at the blastular stage arrested cleavage of these cells with an IC 50 of 0.32 microg/mL.

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