Linderene acetate

CAS# 26146-28-1

Linderene acetate

Catalog No. BCN8042----Order now to get a substantial discount!

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Linderene acetate: 5mg Please Inquire In Stock
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Quality Control of Linderene acetate

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Chemical structure

Linderene acetate

3D structure

Chemical Properties of Linderene acetate

Cas No. 26146-28-1 SDF Download SDF
PubChem ID 497204 Appearance Powder
Formula C17H20O3 M.Wt 272.34
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
SMILES CC1=COC2=C1C(C3C(=C)C4CC4C3(C2)C)OC(=O)C
Standard InChIKey ICLTVELXFUIGLS-FBHBFLDISA-N
Standard InChI InChI=1S/C17H20O3/c1-8-7-19-13-6-17(4)12-5-11(12)9(2)15(17)16(14(8)13)20-10(3)18/h7,11-12,15-16H,2,5-6H2,1,3-4H3/t11-,12-,15-,16+,17+/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 Linderene acetate

The roots of Lindera aggregata

Biological Activity of Linderene acetate

Description1. Linderene acetate is a competitive inhibitor against Prolyl endopeptidase.

Linderene acetate Dilution Calculator

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Linderene acetate Molarity Calculator

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Preparing Stock Solutions of Linderene acetate

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.6719 mL 18.3594 mL 36.7188 mL 73.4376 mL 91.797 mL
5 mM 0.7344 mL 3.6719 mL 7.3438 mL 14.6875 mL 18.3594 mL
10 mM 0.3672 mL 1.8359 mL 3.6719 mL 7.3438 mL 9.1797 mL
50 mM 0.0734 mL 0.3672 mL 0.7344 mL 1.4688 mL 1.8359 mL
100 mM 0.0367 mL 0.1836 mL 0.3672 mL 0.7344 mL 0.918 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 Linderene acetate

Prolyl endopeptidase inhibitors from the roots of Lindera strychnifolia F. Vill.[Pubmed:12186408]

Biol Pharm Bull. 2002 Aug;25(8):1049-52.

Prolyl endopeptidase (PEP, EC 3.4.21.26) has been proposed to play a role in degradation of proline-containing neuropeptides involved in the processes of learning and memory, e.g., vasopressin, substance P, and thyrotropin-releasing hormone (TRH). In the course of our search for bioactive constituents in medicinal plants, we studied the PEP inhibitory constituents of the roots of Lindera strychnifolia F. VILL and isolated two known tannins, epicatechin (1) and aesculitannin B (2), and four known sesquiterpenes, linderene (3), Linderene acetate (4), linderalactone (5) and isolinderalactone (6) as inhibitors. On the inhibitory activities of six compounds against PEP from Flavobacterium meningosepticum and that from rat brain supernatant, compounds 1, 2 and 4 inhibited the enzyme from Flavobacterium more strongly than that from rat brain supernatant. However, compounds 3, 5 and 6 inhibited the enzymes from both origins to the same extent and furthermore, compound 6 was the strongest natural inhibitor against PEP from rat brain supernatant. The kinetic study of these inhibitors indicated that compounds 1, 2 are noncompetitive inhibitors and compounds 3-6 are competitive inhibitors. This is the first example of non-phenolic constituents showing significant competitive inhibitory activity being isolated from natural medicines.

Description

Linderene acetate, isolated from the root of Lindera strychnifolia, is a prolyl endopeptidase inhibitor.

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