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Longipedlactone J

CAS# 1011762-93-8

Longipedlactone J

2D Structure

Catalog No. BCN6644----Order now to get a substantial discount!

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Quality Control of Longipedlactone J

3D structure

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Longipedlactone J

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Chemical Properties of Longipedlactone J

Cas No. 1011762-93-8 SDF Download SDF
PubChem ID 24854383 Appearance Powder
Formula C32H40O7 M.Wt 536.7
Type of Compound Triterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name [(1S,9S,10R,12S,13R,18R)-1-hydroxy-8,8,13-trimethyl-17-methylidene-16-[(1R)-1-[(2R)-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-6-oxo-7-oxatetracyclo[10.7.0.03,9.013,18]nonadeca-2,4,15-trien-10-yl] acetate
SMILES CC1=CCC(OC1=O)C(C)C2=CCC3(C4CC(C5C(=CC4(CC3C2=C)O)C=CC(=O)OC5(C)C)OC(=O)C)C
Standard InChIKey VPYOIPWGVNGDBV-XVLJLTBWSA-N
Standard InChI InChI=1S/C32H40O7/c1-17-8-10-24(38-29(17)35)19(3)22-12-13-31(7)23(18(22)2)16-32(36)15-21-9-11-27(34)39-30(5,6)28(21)25(14-26(31)32)37-20(4)33/h8-9,11-12,15,19,23-26,28,36H,2,10,13-14,16H2,1,3-7H3/t19-,23+,24-,25-,26+,28+,31-,32-/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 Longipedlactone J

The stems of Kadsura heteroclita.

Biological Activity of Longipedlactone J

DescriptionStandard reference
In vitro

Compounds from Kadsura heteroclita and related anti-HIV activity.[Pubmed: 18207206 ]

Phytochemistry. 2008 Mar;69(5):1266-72.


METHODS AND RESULTS:
Phytochemical investigation of the stems of Kadsura heteroclita led to isolation of 16 compounds, including the triterpenoid named Longipedlactone J (2), and two dibenzocyclooctadiene type lignans named heteroclitin I and J (3, 4). Compounds 8-10, 14, and 15 were weakly active as anti-HIV agents, whereas compounds 6 and 12 exhibited moderate anti-HIV activity with EC50 values of 1.6 microg/mL, and 1.4 microg/mL, therapeutic index (TI) values of 52.9, and 65.9, respectively. Their structures were established by spectroscopic methods, including application of 2D NMR techniques and CD spectra.

Longipedlactone J Dilution Calculator

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Longipedlactone J Molarity Calculator

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Preparing Stock Solutions of Longipedlactone J

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.8632 mL 9.3162 mL 18.6324 mL 37.2648 mL 46.581 mL
5 mM 0.3726 mL 1.8632 mL 3.7265 mL 7.453 mL 9.3162 mL
10 mM 0.1863 mL 0.9316 mL 1.8632 mL 3.7265 mL 4.6581 mL
50 mM 0.0373 mL 0.1863 mL 0.3726 mL 0.7453 mL 0.9316 mL
100 mM 0.0186 mL 0.0932 mL 0.1863 mL 0.3726 mL 0.4658 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 Longipedlactone J

Compounds from Kadsura heteroclita and related anti-HIV activity.[Pubmed:18207206]

Phytochemistry. 2008 Mar;69(5):1266-72.

Phytochemical investigation of the stems of Kadsura heteroclita led to isolation of 16 compounds, including the triterpenoid named Longipedlactone J (2), and two dibenzocyclooctadiene type lignans named heteroclitin I and J (3, 4). Compounds 8-10, 14, and 15 were weakly active as anti-HIV agents, whereas compounds 6 and 12 exhibited moderate anti-HIV activity with EC50 values of 1.6 microg/mL, and 1.4 microg/mL, therapeutic index (TI) values of 52.9, and 65.9, respectively. Their structures were established by spectroscopic methods, including application of 2D NMR techniques and CD spectra.

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