Florilenalin

CAS# 54964-49-7

Florilenalin

Catalog No. BCN6422----Order now to get a substantial discount!

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Quality Control of Florilenalin

Number of papers citing our products

Chemical structure

Florilenalin

3D structure

Chemical Properties of Florilenalin

Cas No. 54964-49-7 SDF Download SDF
PubChem ID 442243 Appearance Powder
Formula C15H20O4 M.Wt 264.32
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (3aR,5aS,6S,8R,8aR,9aR)-6,8-dihydroxy-8-methyl-1,5-dimethylidene-3a,4,5a,6,7,8a,9,9a-octahydroazuleno[6,5-b]furan-2-one
SMILES CC1(CC(C2C1CC3C(CC2=C)OC(=O)C3=C)O)O
Standard InChIKey RBLYUGWIFLXCPD-VZGVWICMSA-N
Standard InChI InChI=1S/C15H20O4/c1-7-4-12-9(8(2)14(17)19-12)5-10-13(7)11(16)6-15(10,3)18/h9-13,16,18H,1-2,4-6H2,3H3/t9-,10-,11+,12-,13-,15-/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 Florilenalin

The herbs of Helenium amarum

Protocol of Florilenalin

Structure Identification
Journa of Henan Medical University,1997 (1) :89-93.

Relation between electronic structure and anticancerous activity of florilenalin and rabdocalin A[Reference: WebLink]


METHODS AND RESULTS:
MNDO method was used to achieve the quantum chemical calculation of Florilenalin and rabdocalin A.The front molecular orbitals,orbital energies,bond orders,and atomic charges were obtained.
CONCLUSIONS:
The results showed that α methylene β carbonyl 5 numbered ring was an anticancerous zone.The weakest chemical bond was in this zone which consists of the electrophilic πLUMO orbital.Nucleophilic addition took place when the medical molecules approached their target.The other 5,6 or 7 numbered rings had no anticancerous activities.

Florilenalin Dilution Calculator

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Florilenalin Molarity Calculator

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Preparing Stock Solutions of Florilenalin

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.7833 mL 18.9165 mL 37.8329 mL 75.6659 mL 94.5823 mL
5 mM 0.7567 mL 3.7833 mL 7.5666 mL 15.1332 mL 18.9165 mL
10 mM 0.3783 mL 1.8916 mL 3.7833 mL 7.5666 mL 9.4582 mL
50 mM 0.0757 mL 0.3783 mL 0.7567 mL 1.5133 mL 1.8916 mL
100 mM 0.0378 mL 0.1892 mL 0.3783 mL 0.7567 mL 0.9458 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 Florilenalin

2beta-(Isobutyryloxy)florilenalin, a sesquiterpene lactone isolated from the medicinal plant Centipeda minima, induces apoptosis in human nasopharyngeal carcinoma CNE cells.[Pubmed:19553887]

Molecules. 2009 Jun 12;14(6):2135-46.

Centipeda minima is a medicinal plant reputed in China as a remedy for nasopharyngeal carcinoma (NPC). In this study, bioactivity-guided fractionation of the anti-NPC compound(s) from C. minima led to the isolation of 2beta-(isobutyryloxy)Florilenalin (IF), a sesquiterpene lactone. IF showed significant dose- and time- dependent inhibition on the growth of the human nasopharyngeal carcinoma epithelia cells (CNE). It induced apoptosis in CNE cells, as shown by the accumulation of sub-G1 cell population, DNA fragmentation and nuclear condensation, caspase-3 activation and PARP cleavage. Such induction was associated with the depletion of mitochondrial membrane potential (DeltaPsim) and the release of cytochrome c to cytosol to regulate the expression of Bcl-2 family proteins. These activities led to the cleavage of caspases and the trigger of cell death process. Overall, IF in C. minima showed potent antiproliferative effect of C. minima on NPC cells, suggesting that the plant deserves more extensive investigation for its potential medicinal application.

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