Stachartin C

CAS# 1978388-56-5

Stachartin C

2D Structure

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Stachartin C: 5mg $1150 In Stock
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3D structure

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Stachartin C

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Chemical Properties of Stachartin C

Cas No. 1978388-56-5 SDF Download SDF
PubChem ID 134715094 Appearance Powder
Formula C29H41NO6 M.Wt 499.64
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name methyl 2-[(3R,4aS,7R,8R,8aS)-3,4'-dihydroxy-4,4,7,8a-tetramethyl-6'-oxospiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-3,8-dihydrofuro[2,3-e]isoindole]-7'-yl]-3-methylbutanoate
SMILES CC1CCC2C(C(CCC2(C13CC4=C(C=C5C(=C4O3)CN(C5=O)C(C(C)C)C(=O)OC)O)C)O)(C)C
Standard InChIKey JKWMAZXFGSTHBM-NDVPSALTSA-N
Standard InChI InChI=1S/C29H41NO6/c1-15(2)23(26(34)35-7)30-14-19-17(25(30)33)12-20(31)18-13-29(36-24(18)19)16(3)8-9-21-27(4,5)22(32)10-11-28(21,29)6/h12,15-16,21-23,31-32H,8-11,13-14H2,1-7H3/t16-,21+,22-,23?,28+,29-/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 Stachartin C

The cultures of the tin mine tailings-associated fungus Stachybotrys chartarum.

Biological Activity of Stachartin C

DescriptionStachartin C is a natural product from the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum.

Protocol of Stachartin C

Structure Identification
Helvetica Chimica Acta, 2016, 99(8):583-587.

Stachartins A - E, Phenylspirodrimanes from the Tin Mine Tailings-Associated Fungus Stachybotrys chartarum.[Reference: WebLink]


METHODS AND RESULTS:
Eight phenylspirodrimane-type analogues, including five new compounds, named stachartin A, stachartin B, Stachartin C, stachartin D, Stachartin E (1, 3, 6 - 8), were isolated from cultures of the tin mine tailings-associated fungus Stachybotrys chartarum.
CONCLUSIONS:
Their structures were elucidated by spectroscopic methods including extensive 2D-NMR techniques.

Stachartin C Dilution Calculator

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Stachartin C Molarity Calculator

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Preparing Stock Solutions of Stachartin C

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.0014 mL 10.0072 mL 20.0144 mL 40.0288 mL 50.036 mL
5 mM 0.4003 mL 2.0014 mL 4.0029 mL 8.0058 mL 10.0072 mL
10 mM 0.2001 mL 1.0007 mL 2.0014 mL 4.0029 mL 5.0036 mL
50 mM 0.04 mL 0.2001 mL 0.4003 mL 0.8006 mL 1.0007 mL
100 mM 0.02 mL 0.1001 mL 0.2001 mL 0.4003 mL 0.5004 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 Stachartin C

Stachartins A - E, Phenylspirodrimanes from the Tin Mine Tailings-Associated Fungus Stachybotrys chartarum.

Helvetica Chimica Acta, 2016, 99(8):583-587.

Eight phenylspirodrimane-type analogues, including five new compounds, named stachartin A, stachartin B, Stachartin C, stachartin D, Stachartin E (1, 3, 6 - 8), were isolated from cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. Their structures were elucidated by spectroscopic methods including extensive 2D-NMR techniques.

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