Chloramultilide D

CAS# 1000995-49-2

Chloramultilide D

2D Structure

Catalog No. BCN7102----Order now to get a substantial discount!

Product Name & Size Price Stock
Chloramultilide D: 5mg $886 In Stock
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Quality Control of Chloramultilide D

3D structure

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Chloramultilide D

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Chemical Properties of Chloramultilide D

Cas No. 1000995-49-2 SDF Download SDF
PubChem ID 24763323 Appearance Powder
Formula C35H40O11 M.Wt 636.69
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
SMILES CC=C(C)C(=O)OCC1(C2CC2C3(C1CC4=C(C(=O)OC45C3CC6(C7CC7C8(C6=C5C9=C(C(=O)OC9(C8O)O)C)C)O)CO)C)O
Standard InChIKey JDNYCIQWGHMSPJ-ANOWQDLRSA-N
Standard InChI InChI=1S/C35H40O11/c1-6-13(2)26(37)44-12-33(42)20-7-17(20)30(4)21(33)9-16-15(11-36)28(39)45-34(16)22(30)10-32(41)19-8-18(19)31(5)25(32)24(34)23-14(3)27(38)46-35(23,43)29(31)40/h6,17-22,29,36,40-43H,7-12H2,1-5H3/b13-6+/t17-,18-,19+,20+,21-,22+,29-,30+,31+,32+,33+,34+,35+/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 Chloramultilide D

The whole plants of Chloranthus spicatus.

Biological Activity of Chloramultilide D

DescriptionChloramultilide D is a natural product from Chloranthus spicatus.

Protocol of Chloramultilide D

Structure Identification
J Nat Prod. 2007 Dec;70(12):1987-90

Mono- and Di-sesquiterpenoids from Chloranthus spicatus.[Pubmed: 18044839 ]


METHODS AND RESULTS:
Three new dimeric sesquiterpenoids, chloramultilide B, chloramultilide C, Chloramultilide D ( 1- 3), along with 10 known sesquiterpenoids, were isolated from the whole plant of Chloranthus spicatus. Their structures were established by physical data (1D and 2D NMR, MS).
CONCLUSIONS:
The structure and absolute configuration of 1 was confirmed by X-ray crystallography. Compound 1 exhibited moderate in vitro antifungal activity.

Chloramultilide D Dilution Calculator

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Chloramultilide D Molarity Calculator

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Preparing Stock Solutions of Chloramultilide D

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.5706 mL 7.8531 mL 15.7062 mL 31.4125 mL 39.2656 mL
5 mM 0.3141 mL 1.5706 mL 3.1412 mL 6.2825 mL 7.8531 mL
10 mM 0.1571 mL 0.7853 mL 1.5706 mL 3.1412 mL 3.9266 mL
50 mM 0.0314 mL 0.1571 mL 0.3141 mL 0.6282 mL 0.7853 mL
100 mM 0.0157 mL 0.0785 mL 0.1571 mL 0.3141 mL 0.3927 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 Chloramultilide D

Mono- and Di-sesquiterpenoids from Chloranthus spicatus.[Pubmed:18044839]

J Nat Prod. 2007 Dec;70(12):1987-90.

Three new dimeric sesquiterpenoids, chloramultilides B-D ( 1- 3), along with 10 known sesquiterpenoids, were isolated from the whole plant of Chloranthus spicatus. Their structures were established by physical data (1D and 2D NMR, MS). The structure and absolute configuration of 1 was confirmed by X-ray crystallography. Compound 1 exhibited moderate in vitro antifungal activity.

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