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Chloranthalactone E

CAS# 73215-92-6

Chloranthalactone E

2D Structure

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Chloranthalactone E: 5mg $799 In Stock
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Quality Control of Chloranthalactone E

3D structure

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Chloranthalactone E

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Chemical Properties of Chloranthalactone E

Cas No. 73215-92-6 SDF Download SDF
PubChem ID 131676069 Appearance Powder
Formula C15H18O4 M.Wt 262.30
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (1S,7R,8S,9S,10R,12S)-7,8-dihydroxy-4,9-dimethyl-13-methylidene-6-oxatetracyclo[7.4.0.03,7.010,12]tridec-3-en-5-one
SMILES CC1=C2CC3C(=C)C4CC4C3(C(C2(OC1=O)O)O)C
Standard InChIKey LJLXBYGPGVKTBK-NRLMIDHWSA-N
Standard InChI InChI=1S/C15H18O4/c1-6-8-4-11(8)14(3)9(6)5-10-7(2)12(16)19-15(10,18)13(14)17/h8-9,11,13,17-18H,1,4-5H2,2-3H3/t8-,9+,11-,13+,14-,15-/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 Chloranthalactone E

The roots of Chloranthus serratus.

Biological Activity of Chloranthalactone E

DescriptionChloranthalactone E is a natural product from Chloranthus serratus.

Protocol of Chloranthalactone E

Structure Identification
Zhong Yao Cai. 2015 Oct;38(10):2087-90.

Sesquiterpenes of Chloranthus serratus Root.[Pubmed: 27254920]

To study sesquiterpenes from the root of Chloranthus serratus.
METHODS AND RESULTS:
The sesquiterpenes of Chloranthus serratus were isolated and purified by various chromatographic techniques, such as silica gel, Sephadex LH-20 and preparative HPLC. The structures of these isolated compounds were identified by spectroscopic analysis. Ten sesquiterpenes were isolated and identified as follows: 1β, 8β-dihydroxy-eudesman-4 (15), 7 (11) -dien-8α, 12-olide (I), curcolonol (II), 4β, 8β-dihydroxy-5α (H) -eudesm-7 (11) -en-8, 12-olide (III), 1β, 8,β-dihydroxy-eudesman-3, 7 (11) -dien-8α, 12-olide (IV), multistalactone E (V), zedoarofuran (VI), 8β,9α-dihydroxylindan-4(5), 7(11) -dien-8α,12-olide(VII), serralactone A (VIII), 8-epi-ivangustin (IX), and Chloranthalactone E (X ).
CONCLUSIONS:
Compounds I, II, IV - VII, IX and X are isolated from Chloranthus serratus for the first time.

Chloranthalactone E Dilution Calculator

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Preparing Stock Solutions of Chloranthalactone E

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.8124 mL 19.0621 mL 38.1243 mL 76.2486 mL 95.3107 mL
5 mM 0.7625 mL 3.8124 mL 7.6249 mL 15.2497 mL 19.0621 mL
10 mM 0.3812 mL 1.9062 mL 3.8124 mL 7.6249 mL 9.5311 mL
50 mM 0.0762 mL 0.3812 mL 0.7625 mL 1.525 mL 1.9062 mL
100 mM 0.0381 mL 0.1906 mL 0.3812 mL 0.7625 mL 0.9531 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 Chloranthalactone E

[Sesquiterpenes of Chloranthus serratus Root].[Pubmed:27254920]

Zhong Yao Cai. 2015 Oct;38(10):2087-90.

OBJECTIVE: To study sesquiterpenes from the root of Chloranthus serratus. METHODS: The sesquiterpenes of Chloranthus serratus were isolated and purified by various chromatographic techniques, such as silica gel, Sephadex LH-20 and preparative HPLC. The structures of these isolated compounds were identified by spectroscopic analysis. RESULTS: Ten sesquiterpenes were isolated and identified as follows: 1beta, 8beta-dihydroxy-eudesman-4 (15), 7 (11) -dien-8alpha, 12-olide (I), curcolonol (II), 4beta, 8beta-dihydroxy-5alpha (H) -eudesm-7 (11) -en-8, 12-olide (III), 1beta, 8,beta-dihydroxy-eudesman-3, 7 (11) -dien-8alpha, 12-olide (IV), multistalactone E (V), zedoarofuran (VI), 8beta,9alpha-dihydroxylindan-4(5), 7(11) -dien-8alpha,12-olide(VII), serralactone A (VIII), 8-epi-ivangustin (IX), and Chloranthalactone E (X ). CONCLUSION: Compounds I, II, IV - VII, IX and X are isolated from Chloranthus serratus for the first time.

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