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3-Epicabraleahydroxylactone

CAS# 35833-72-8

3-Epicabraleahydroxylactone

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Chemical structure

3-Epicabraleahydroxylactone

3D structure

Chemical Properties of 3-Epicabraleahydroxylactone

Cas No. 35833-72-8 SDF Download SDF
PubChem ID 12080691 Appearance Powder
Formula C27H44O3 M.Wt 416.6
Type of Compound Triterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (5S)-5-[(3S,5R,8R,9R,10R,13R,14R,17S)-3-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-5-methyloxolan-2-one
SMILES CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C5(CCC(=O)O5)C)C)C)C
Standard InChIKey AHDUWGQSZYSNEY-BWNRNTQFSA-N
Standard InChI InChI=1S/C27H44O3/c1-23(2)19-10-15-26(5)20(24(19,3)13-11-21(23)28)8-7-17-18(9-14-25(17,26)4)27(6)16-12-22(29)30-27/h17-21,28H,7-16H2,1-6H3/t17-,18+,19+,20-,21+,24+,25-,26-,27+/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 3-Epicabraleahydroxylactone

The seeds of Melia azedarach.

Biological Activity of 3-Epicabraleahydroxylactone

Description1. 3-Epicabraleahydroxylactone has anti-tumor promoting effect. 2. 3-Epicabraleahydroxylactone has anti-carcinogenic activity by the inhibitory effect on the induction of Epstein-Barr virus early antigen(EBV-EA) by the tumor promoter.

3-Epicabraleahydroxylactone Dilution Calculator

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3-Epicabraleahydroxylactone Molarity Calculator

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Preparing Stock Solutions of 3-Epicabraleahydroxylactone

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.4004 mL 12.0019 mL 24.0038 mL 48.0077 mL 60.0096 mL
5 mM 0.4801 mL 2.4004 mL 4.8008 mL 9.6015 mL 12.0019 mL
10 mM 0.24 mL 1.2002 mL 2.4004 mL 4.8008 mL 6.001 mL
50 mM 0.048 mL 0.24 mL 0.4801 mL 0.9602 mL 1.2002 mL
100 mM 0.024 mL 0.12 mL 0.24 mL 0.4801 mL 0.6001 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 3-Epicabraleahydroxylactone

3-epicabraleahydroxylactone and other triterpenoids from camellia oil and their inhibitory effects on Epstein-Barr virus activation.[Pubmed:14709887]

Chem Pharm Bull (Tokyo). 2004 Jan;52(1):153-6.

The structure of a triterpenoid isolated from the nonsaponifiable lipid (NSL) of the seed oil of the camellia (Camellia japonica L.; Theaceae) was established to be (20S)-3beta-hydroxy-25,26,27-trisnordammaran-24,20-olide (1; 3-Epicabraleahydroxylactone) on the basis of spectroscopic and chemical methods. Six other triterpenoids isolated from the NSL were identified as 3-epicabraleadiol (2), ocotillol II (3), ocotillol I (4), dammarenediol II (5), (20R)-taraxastane-3beta,20-diol (6), and lupane-3beta,20-diol (7). Upon evaluation of the seven triterpenoids (1-7) with respect to their inhibitory effects on the induction of Epstein-Barr virus early antigen (EBV-EA) by 12-O-tetradecanoylphorbol-13-acetate (TPA) in Raji cells, three compounds (5-7) showed potent inhibitory effects against EBV-EA induction (IC(50) values of 277-420 mol ratio/32 pmol TPA).

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