Chartarlactam A

CAS# 1528745-88-1

Chartarlactam A

Catalog No. BCN7110----Order now to get a substantial discount!

Product Name & Size Price Stock
Chartarlactam A:5mg Please Inquire In Stock
Chartarlactam A:10mg Please Inquire In Stock
Chartarlactam A:20mg Please Inquire In Stock
Chartarlactam A:50mg Please Inquire In Stock

Quality Control of Chartarlactam A

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Chemical structure

Chartarlactam A

3D structure

Chemical Properties of Chartarlactam A

Cas No. 1528745-88-1 SDF Download SDF
PubChem ID 76328314 Appearance Powder
Formula C23H29NO5 M.Wt 399.48
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'-3H-furo[2,3-e]isoindole]-6',8'-dione
SMILES CC1CCC2C(C(CCC2(C13CC4=C(C=C5C(=C4O3)C(=O)NC5=O)O)C)O)(C)C
Standard InChIKey JGLXRTLGZYXTLO-NMBLNHEASA-N
Standard InChI InChI=1S/C23H29NO5/c1-11-5-6-15-21(2,3)16(26)7-8-22(15,4)23(11)10-13-14(25)9-12-17(18(13)29-23)20(28)24-19(12)27/h9,11,15-16,25-26H,5-8,10H2,1-4H3,(H,24,27,28)/t11-,15+,16-,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 Chartarlactam A

The solid cultures of Stachybotrys chartarum.

Biological Activity of Chartarlactam A

Description1. Chartarlactam A shows antihyperlipidemic effects in HepG2 cells.

Chartarlactam A Dilution Calculator

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Chartarlactam A Molarity Calculator

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Preparing Stock Solutions of Chartarlactam A

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.5033 mL 12.5163 mL 25.0325 mL 50.0651 mL 62.5814 mL
5 mM 0.5007 mL 2.5033 mL 5.0065 mL 10.013 mL 12.5163 mL
10 mM 0.2503 mL 1.2516 mL 2.5033 mL 5.0065 mL 6.2581 mL
50 mM 0.0501 mL 0.2503 mL 0.5007 mL 1.0013 mL 1.2516 mL
100 mM 0.025 mL 0.1252 mL 0.2503 mL 0.5007 mL 0.6258 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 Chartarlactam A

Chartarlactams A-P, phenylspirodrimanes from the sponge-associated fungus Stachybotrys chartarum with antihyperlipidemic activities.[Pubmed:24387683]

J Nat Prod. 2014 Jan 24;77(1):138-47.

Chemical examination of the solid culture of the endophytic fungus Stachybotrys chartarum isolated from the sponge Niphates recondita resulted in the isolation of 16 new phenylspirodrimanes, named chartarlactams A-P (1-16), together with eight known analogues. Their structures were determined on the basis of extensive spectroscopic analysis, including X-ray single-crystal diffraction for the determination of the absolute configurations. The isoindolone-drimane dimer chartarlactam L (12) was determined as a new skeleton. Compounds 1-6 and 8-24 were evaluated for antihyperlipidemic effects in HepG2 cells, and the primary structure-activity relationships are discussed.

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