Alpinenone

CAS# 103425-23-6

Alpinenone

2D Structure

Catalog No. BCX0464----Order now to get a substantial discount!

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Alpinenone

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Chemical Properties of Alpinenone

Cas No. 103425-23-6 SDF Download SDF
PubChem ID N/A Appearance Powder
Formula C15H22O3 M.Wt 250.37
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
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.

Alpinenone Dilution Calculator

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Alpinenone Molarity Calculator

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Preparing Stock Solutions of Alpinenone

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.9941 mL 19.9704 mL 39.9409 mL 79.8818 mL 99.8522 mL
5 mM 0.7988 mL 3.9941 mL 7.9882 mL 15.9764 mL 19.9704 mL
10 mM 0.3994 mL 1.997 mL 3.9941 mL 7.9882 mL 9.9852 mL
50 mM 0.0799 mL 0.3994 mL 0.7988 mL 1.5976 mL 1.997 mL
100 mM 0.0399 mL 0.1997 mL 0.3994 mL 0.7988 mL 0.9985 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 Alpinenone

Terpenoids from Nardostachys jatamansi and their cytotoxic activity against human pancreatic cancer cell lines.[Pubmed:35561851]

Phytochemistry. 2022 Aug;200:113228.

Five previously unreported terpenoids, together with fifteen known analogs, were isolated from a methanol extract of the roots and rhizomes of Nardostachys jatamansi. Their structures, including absolute configurations, were elucidated by spectroscopic data and electronic circular dichroism (ECD) spectra analyses, as well as single-crystal X-ray diffraction for crystalline compounds. Structurally, (4R,5S,6S,7R)-1(10)-aristolane-8,9-diacid is a novel 8,9-dicarboxylic acid derivative of aristolane-type sesquiterpenoid. (4R,6S,7R,10S)-10-Hydroxyguaia-1(5)-6,7-epoxy-2-one is an undescribed analogue of nardoguaianone K, with a rare 6,7-epoxide group. (4R,5R,6R,8R)-1(10)-Isonardosinone-8-ol-9-one-7,11-lactone is an isonardosinane-type sesquiterpene bearing a gamma-lactone ring. Dinardokanshone F is a rare example of a sesquiterpene dimer from N. jatamansi connected by an oxo bridge. The isolates were evaluated for their cytotoxic activity against four human pancreatic cancer cell lines (CFPAC-1, PANC-1, CAPAN-2 and SW1990). Compound epoxynardosinone exhibited significant cytotoxicity against CAPAN-2 cell lines with IC(50) value of 2.60 +/- 1.85 muM. 1-Hydroxylaristolone displayed comparable cytotoxicity on CFPAC-1 cell lines (IC(50) 1.12 +/- 1.19 muM), compared to Taxol (IC(50) 0.32 +/- 0.13 muM). 1-Hydroxylaristolone, 1(10)-aristolane-9beta-ol, 1(10)-aristolen-2-one, Alpinenone, valtrate isovaleroyloxyhydrine and nardostachin displayed stronger cytotoxicity against PANC-1 cell lines with IC(50) values ranging from 0.01 +/- 0.01 to 6.50 +/- 1.10 muM. 1(10)-Aristolane-9beta-ol, 10-hydroxyguaia-1(5)-6,7-epoxy-2-one, nardoguaianone K, nardonoxide, epoxynardosinone, 1(10)-isonardosinone-8-ol-9-one-7,11-lactone, valtrate isovaleroyloxyhydrine and nardostachin showed remarkable cytotoxicity against SW1990 cell lines with IC(50) values ranging from 0.07 +/- 0.05 to 4.82 +/- 6.96 muM. Furthermore, the primary mechanistic study of nardostachin demonstrated that it induced cell apoptosis via the mitochondria-dependent pathway, and induced SW1900 cell arrest at G2/M phase.

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