Shizukanolide H

CAS# 1136932-34-7

Shizukanolide H

Catalog No. BCN6016----Order now to get a substantial discount!

Product Name & Size Price Stock
Shizukanolide H: 5mg $886 In Stock
Shizukanolide H: 10mg Please Inquire In Stock
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Quality Control of Shizukanolide H

Number of papers citing our products

Chemical structure

Shizukanolide H

3D structure

Chemical Properties of Shizukanolide H

Cas No. 1136932-34-7 SDF Download SDF
PubChem ID 91885103 Appearance Powder
Formula C17H20O5 M.Wt 304.3
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
SMILES CC(=O)OCC1C2CC2C3(C1CC4=C(C(=O)OC4=C3)CO)C
Standard InChIKey SVHYJRPBSSMUDB-SRIVDKISSA-N
Standard InChI InChI=1S/C17H20O5/c1-8(19)21-7-12-9-3-13(9)17(2)5-15-10(4-14(12)17)11(6-18)16(20)22-15/h5,9,12-14,18H,3-4,6-7H2,1-2H3/t9-,12-,13-,14+,17+/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 Shizukanolide H

The herbs of Chloranthus spicatus

Biological Activity of Shizukanolide H

DescriptionStandard reference

Protocol of Shizukanolide H

Structure Identification
Chin J Nat Med. 2012 Jan;10(1):24-7.

A new eudesmane sesquiterpenoid lactone from Chloranthus japonicus.[Pubmed: 23302525]

To study the chemical constituents of the whole plant of Chloranthus japonicus.
METHODS AND RESULTS:
Compounds were isolated and purified by column chromatography. Their structures were elucidated on the basis of spectroscopic methods.Six sesquiterpenoids were obtained and their structures were identified as chlojaponilactone A (1), atractylenolide III (2), neolitacumone B (3), 10α-hydroxy-1-oxoeremophila-7(11), 8(9)-diene-8, 12-olide (4), shizukanolide C (5), and Shizukanolide H (6).
CONCLUSIONS:
Compound 1 is a new eudesmane-type sesquiterpenoid lactone, and compounds 3 and 4 have been isolated from this species for the first time.

Shizukanolide H Dilution Calculator

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Shizukanolide H Molarity Calculator

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Preparing Stock Solutions of Shizukanolide H

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.2862 mL 16.4312 mL 32.8623 mL 65.7246 mL 82.1558 mL
5 mM 0.6572 mL 3.2862 mL 6.5725 mL 13.1449 mL 16.4312 mL
10 mM 0.3286 mL 1.6431 mL 3.2862 mL 6.5725 mL 8.2156 mL
50 mM 0.0657 mL 0.3286 mL 0.6572 mL 1.3145 mL 1.6431 mL
100 mM 0.0329 mL 0.1643 mL 0.3286 mL 0.6572 mL 0.8216 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 Shizukanolide H

A new eudesmane sesquiterpenoid lactone from Chloranthus japonicus.[Pubmed:23302525]

Chin J Nat Med. 2012 Jan;10(1):24-7.

AIM: To study the chemical constituents of the whole plant of Chloranthus japonicus. METHODS: Compounds were isolated and purified by column chromatography. Their structures were elucidated on the basis of spectroscopic methods. RESULTS: Six sesquiterpenoids were obtained and their structures were identified as chlojaponilactone A (1), atractylenolide III (2), neolitacumone B (3), 10alpha-hydroxy-1-oxoeremophila-7(11), 8(9)-diene-8, 12-olide (4), shizukanolide C (5), and Shizukanolide H (6). CONCLUSION: Compound 1 is a new eudesmane-type sesquiterpenoid lactone, and compounds 3 and 4 have been isolated from this species for the first time.

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