Anisofolin A

CAS# 83529-71-9

Anisofolin A

Catalog No. BCN4377----Order now to get a substantial discount!

Product Name & Size Price Stock
Anisofolin A: 5mg $966 In Stock
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Quality Control of Anisofolin A

Number of papers citing our products

Chemical structure

Anisofolin A

3D structure

Chemical Properties of Anisofolin A

Cas No. 83529-71-9 SDF Download SDF
PubChem ID 21721971 Appearance Yellow powder
Formula C39H32O14 M.Wt 724.7
Type of Compound Flavonoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name [(2R,3R,4S,5R,6S)-3,5-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate
SMILES C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O
Standard InChIKey LHMKSPOTCLVAKR-AVMIHGAISA-N
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 Anisofolin A

The herbs of Leonurus japonicus

Biological Activity of Anisofolin A

Description1. Anisofolin A has promising antimalarial activity (IC50 4.39 ± 0.25 uM). 2. Anisofolin A has promising antimycobacterium activity [IC50 4.50 ± 0.75 uM (3.31 ug/mL)] against M. tuberculosis H37Ra and at 100 ug/mL, shows 55.6 % inhibition of M. bovis.
TargetsAntifection

Anisofolin A Dilution Calculator

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Anisofolin A Molarity Calculator

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Preparing Stock Solutions of Anisofolin A

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.3799 mL 6.8994 mL 13.7988 mL 27.5976 mL 34.497 mL
5 mM 0.276 mL 1.3799 mL 2.7598 mL 5.5195 mL 6.8994 mL
10 mM 0.138 mL 0.6899 mL 1.3799 mL 2.7598 mL 3.4497 mL
50 mM 0.0276 mL 0.138 mL 0.276 mL 0.552 mL 0.6899 mL
100 mM 0.0138 mL 0.069 mL 0.138 mL 0.276 mL 0.345 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 Anisofolin A

Studies on Nepalese crude drugs. XXIX. Chemical constituents of Dronapuspi, the whole herb of Leucas cephalotes SPRENG.[Pubmed:17015972]

Chem Pharm Bull (Tokyo). 2006 Oct;54(10):1370-9.

From the whole herb of Leucas cephalotes SPRENG., new labdane-, norlabdane- and abietane-type diterpenes named leucasdins A (1), B (2) and C (3), respectively, and two protostane-type triterpenes named leucastrins A (4) and B (5) were isolated, together with a known triterpene, oleanolic acid, five sterols, 7-oxositosterol, 7-oxostigmasterol, 7alpha-hydroxysitosterol, 7alpha-hydroxystigmasterol and stigmasterol, and eight flavones, 5-hydroxy-7,4'-dimethoxyflavone, pillion, gonzalitosin I, tricin, cosmosin, apigenin 7-O-beta-D-(6-O-p-coumaroyl)glucopyranoside, Anisofolin A and luteolin 4'-O-beta-D-glucuronopyranoside. The structures of 1--5 were determined as (3S,6R,8R,9R,13S,16S)-9,13,15,16-bisepoxy-3,16-diacetoxy-6-formyloxylabdane, (3S,6R)-3-acetoxy-6-formyloxy-iso-ambreinolide, (4R,9S,12R,13R)-12,13-dihydroxyabiet-7-en-18-oic acid, (3S,17S,20S,24S)-3,20-dihydroxy-24-methylprotost-25-en, and (3S,17S,20S,24S)-3,20,24-trihydroxyprotost-25-en respectively, based on spectral and chemical data.

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