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20-Hydroxyaflavinine

CAS# 116865-08-8

20-Hydroxyaflavinine

2D Structure

Catalog No. BCN7283----Order now to get a substantial discount!

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3D structure

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20-Hydroxyaflavinine

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Chemical Properties of 20-Hydroxyaflavinine

Cas No. 116865-08-8 SDF Download SDF
PubChem ID 124511201 Appearance Powder
Formula C28H39NO2 M.Wt 421.62
Type of Compound Diterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (1S,4R,4aS,5R,7R,7aS,11aS)-8-(1H-indol-3-yl)-4,4a,7-trimethyl-9-propan-2-yl-1,2,3,4,5,6,7,7a,10,11-decahydrobenzo[d]naphthalene-1,5-diol
SMILES CC1CCC(C23C1(C(CC(C2C(=C(CC3)C(C)C)C4=CNC5=CC=CC=C54)C)O)C)O
Standard InChIKey GVGMWTZTHQRHRE-GSJQUQQQSA-N
Standard InChI InChI=1S/C28H39NO2/c1-16(2)19-12-13-28-23(30)11-10-18(4)27(28,5)24(31)14-17(3)26(28)25(19)21-15-29-22-9-7-6-8-20(21)22/h6-9,15-18,23-24,26,29-31H,10-14H2,1-5H3/t17-,18-,23+,24-,26+,27-,28+/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 20-Hydroxyaflavinine

The metabolites of the ascomycete fungus Tricladium sp.

Biological Activity of 20-Hydroxyaflavinine

Description20-Hydroxyaflavinine is a natural product from the metabolites of the ascomycete fungus Tricladium sp.
In vitro

Two new imidazolone-containing alkaloids and further metabolites from the ascomycete fungus Tricladium sp.[Pubmed: 22006720 ]

Chem Biodivers. 2011 Oct;8(10):1914-20.


METHODS AND RESULTS:
Tricladins A and B (1 and 2, resp.), new imidazolone-containing alkaloids, together with five known metabolites, bacillamides A, B (3 and 4, resp.), 20-Hydroxyaflavinine (5), N-(2-phenylethyl)acetamide (6), and N(b)-acetyltryptamine (7), have been isolated from the crude extract of the ascomycete fungus Tricladium sp. The structures of 1 and 2 were elucidated primarily by NMR and MS methods.
CONCLUSIONS:
Compound 2 showed marginal cytotoxicity against MDA-MB-231 human breast cancer cells, whereas the known metabolite 4 displayed an inhibitory effect on HIV-1 replication in C8166 cells.

20-Hydroxyaflavinine Dilution Calculator

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Preparing Stock Solutions of 20-Hydroxyaflavinine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.3718 mL 11.859 mL 23.718 mL 47.4361 mL 59.2951 mL
5 mM 0.4744 mL 2.3718 mL 4.7436 mL 9.4872 mL 11.859 mL
10 mM 0.2372 mL 1.1859 mL 2.3718 mL 4.7436 mL 5.9295 mL
50 mM 0.0474 mL 0.2372 mL 0.4744 mL 0.9487 mL 1.1859 mL
100 mM 0.0237 mL 0.1186 mL 0.2372 mL 0.4744 mL 0.593 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 20-Hydroxyaflavinine

Two new imidazolone-containing alkaloids and further metabolites from the ascomycete fungus Tricladium sp.[Pubmed:22006720]

Chem Biodivers. 2011 Oct;8(10):1914-20.

Tricladins A and B (1 and 2, resp.), new imidazolone-containing alkaloids, together with five known metabolites, bacillamides A, B (3 and 4, resp.), 20-Hydroxyaflavinine (5), N-(2-phenylethyl)acetamide (6), and N(b)-acetyltryptamine (7), have been isolated from the crude extract of the ascomycete fungus Tricladium sp. The structures of 1 and 2 were elucidated primarily by NMR and MS methods. Compound 2 showed marginal cytotoxicity against MDA-MB-231 human breast cancer cells, whereas the known metabolite 4 displayed an inhibitory effect on HIV-1 replication in C8166 cells.

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