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Isoapetalic acid

CAS# 34366-34-2

Isoapetalic acid

Catalog No. BCN5276----Order now to get a substantial discount!

Product Name & Size Price Stock
Isoapetalic acid:5mg Please Inquire In Stock
Isoapetalic acid:10mg Please Inquire In Stock
Isoapetalic acid:20mg Please Inquire In Stock
Isoapetalic acid:50mg Please Inquire In Stock

Quality Control of Isoapetalic acid

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Chemical structure

Isoapetalic acid

3D structure

Chemical Properties of Isoapetalic acid

Cas No. 34366-34-2 SDF Download SDF
PubChem ID 3012917 Appearance Powder
Formula C22H28O6 M.Wt 388.5
Type of Compound Flavonoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 3-[(7S,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]hexanoic acid
SMILES CCCC(CC(=O)O)C1=C2C(=C(C3=C1OC(C=C3)(C)C)O)C(=O)C(C(O2)C)C
Standard InChIKey JZWLSXINEVHWEP-VYAYZGMFSA-N
Standard InChI InChI=1S/C22H28O6/c1-6-7-13(10-15(23)24)16-20-14(8-9-22(4,5)28-20)19(26)17-18(25)11(2)12(3)27-21(16)17/h8-9,11-13,26H,6-7,10H2,1-5H3,(H,23,24)/t11-,12-,13?/m0/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 Isoapetalic acid

The leaves of Calophyllum brasiliense

Biological Activity of Isoapetalic acid

Description1. Isoapetalic acid and apetalic acid exhibit cytotoxic activities towards both cancer cell lines(human breast cancer (MCF-7) and human lung carcinoma (A-549) cell lines) and both Gram-positive bacteria(two Gram-positive bacteria, S. aureus and B. subtilis and two Gram-negative bacteria, P. aeruginosa and E. coli.).
TargetsAntifection

Isoapetalic acid Dilution Calculator

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Isoapetalic acid Molarity Calculator

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Preparing Stock Solutions of Isoapetalic acid

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.574 mL 12.87 mL 25.74 mL 51.4801 mL 64.3501 mL
5 mM 0.5148 mL 2.574 mL 5.148 mL 10.296 mL 12.87 mL
10 mM 0.2574 mL 1.287 mL 2.574 mL 5.148 mL 6.435 mL
50 mM 0.0515 mL 0.2574 mL 0.5148 mL 1.0296 mL 1.287 mL
100 mM 0.0257 mL 0.1287 mL 0.2574 mL 0.5148 mL 0.6435 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 Isoapetalic acid

HIV-1 inhibitory compounds from Calophyllum brasiliense leaves.[Pubmed:15340243]

Biol Pharm Bull. 2004 Sep;27(9):1471-5.

The hexane, acetone and methanol extracts of Calophyllum brasiliense leaves were fractionated following a three bioassay guide: high HIV-1 RT inhibition, low cytotoxicity on MT2 cells and high inhibition of HIV-1 IIIb/LAV replication. This led to the isolation of three anti HIV-1 dipyranocoumarins: calanolides A and B and soulattrolide. In contrast, other isolated compounds such as apetalic acid, Isoapetalic acid, a structural isomer of Isoapetalic acid, friedelin, canophyllol and amentoflavone were devoid of HIV-1 RT inhibitory activity. Calanolide C was also obtained as a natural product and showed moderate inhibitory properties.

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