Stachybotrolide

CAS# 149691-31-6

Stachybotrolide

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Product Name & Size Price Stock
Stachybotrolide: 5mg $989 In Stock
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Quality Control of Stachybotrolide

Number of papers citing our products

Chemical structure

Stachybotrolide

3D structure

Chemical Properties of Stachybotrolide

Cas No. 149691-31-6 SDF Download SDF
PubChem ID 11383606 Appearance Powder
Formula C23H30O5 M.Wt 386.49
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (3R,4aS,7R,8R,8aS)-3,4'-dihydroxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-3,8-dihydrofuro[3,4-g][1]benzofuran]-6'-one
SMILES CC1CCC2C(C(CCC2(C13CC4=C(C=C5C(=C4O3)COC5=O)O)C)O)(C)C
Standard InChIKey HKNSYAPUOMHZDE-RCJATNNHSA-N
Standard InChI InChI=1S/C23H30O5/c1-12-5-6-17-21(2,3)18(25)7-8-22(17,4)23(12)10-14-16(24)9-13-15(19(14)28-23)11-27-20(13)26/h9,12,17-18,24-25H,5-8,10-11H2,1-4H3/t12-,17+,18-,22+,23-/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 Stachybotrolide

The products of Stachybotrys alternans.

Biological Activity of Stachybotrolide

DescriptionStachybotrolide is a natural product from Stachybotrys alternans.

Protocol of Stachybotrolide

Structure Identification
Chemistry of Natural Compounds, 1998, 34(5):616-619.

Low-molecular-mass metabolites of fungi. III. Stachybotrolide from Stachybotrys alternans[Reference: WebLink]


METHODS AND RESULTS:
The new nitrogen-free compound Stachybotrolide has been detected among the products of the vital activity of Stachybotrys alternans . The structure of Stachybotrolide has been determined on the basis of IR, mass, and 1 H and 13 C NMR spectra.
CONCLUSIONS:
To interpret the latter we have made use of DEPT, 2M NMR 1 H61 1 H chemical shift correlation ( 1 H61 1 H COSY or HMQC) and 2M NMR correlations of 1 H61 13 C long-range interactions (HMBC).

Stachybotrolide Dilution Calculator

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Stachybotrolide Molarity Calculator

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Preparing Stock Solutions of Stachybotrolide

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.5874 mL 12.9369 mL 25.8739 mL 51.7478 mL 64.6847 mL
5 mM 0.5175 mL 2.5874 mL 5.1748 mL 10.3496 mL 12.9369 mL
10 mM 0.2587 mL 1.2937 mL 2.5874 mL 5.1748 mL 6.4685 mL
50 mM 0.0517 mL 0.2587 mL 0.5175 mL 1.035 mL 1.2937 mL
100 mM 0.0259 mL 0.1294 mL 0.2587 mL 0.5175 mL 0.6468 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 Stachybotrolide

Low-molecular-mass metabolites of fungi. III. Stachybotrolide from Stachybotrys alternans

Chemistry of Natural Compounds, 1998, 34(5):616-619.

The new nitrogen-free compound Stachybotrolide has been detected among the products of the vital activity of Stachybotrys alternans . The structure of Stachybotrolide has been determined on the basis of IR, mass, and 1 H and 13 C NMR spectra. To interpret the latter we have made use of DEPT, 2M NMR 1 H61 1 H chemical shift correlation ( 1 H61 1 H COSY or HMQC) and 2M NMR correlations of 1 H61 13 C long-range interactions (HMBC).

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