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2-Deoxokanshone M

CAS# 3062873-62-2

2-Deoxokanshone M

2D Structure

Catalog No. BCX2250----Order now to get a substantial discount!

Product Name & Size Price Stock
2-Deoxokanshone M: 5mg $400 In Stock
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2-Deoxokanshone M: 1000mg Please Inquire Please Inquire

Quality Control of 2-Deoxokanshone M

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2-Deoxokanshone M

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Chemical Properties of 2-Deoxokanshone M

Cas No. 3062873-62-2 SDF File under preparation.
PubChem ID N/A Appearance Powder
Formula C12H16O2 M.Wt 192.3
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.

Source of 2-Deoxokanshone M

The roots of Nardostachys jatamansi DC.

2-Deoxokanshone M Dilution Calculator

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2-Deoxokanshone M Molarity Calculator

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Preparing Stock Solutions of 2-Deoxokanshone M

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.2002 mL 26.001 mL 52.0021 mL 104.0042 mL 130.0052 mL
5 mM 1.04 mL 5.2002 mL 10.4004 mL 20.8008 mL 26.001 mL
10 mM 0.52 mL 2.6001 mL 5.2002 mL 10.4004 mL 13.0005 mL
50 mM 0.104 mL 0.52 mL 1.04 mL 2.0801 mL 2.6001 mL
100 mM 0.052 mL 0.26 mL 0.52 mL 1.04 mL 1.3001 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 2-Deoxokanshone M

Degradation Profiling of Nardosinone at High Temperature and in Simulated Gastric and Intestinal Fluids.[Pubmed:37513256]

Molecules. 2023 Jul 13;28(14):5382.

Nardosinone, a predominant bioactive product from Nardostachys jatamansi DC, is well-known for its promising therapeutic applications, such as being used as a drug on anti-inflammatory, antidepressant, cardioprotective, anti-neuroinflammatory, anti-arrhythmic, anti-periodontitis, etc. However, its stability under varying environmental conditions and its degradation products remain unclear. In this study, four main degradation products, including two previously undescribed compounds [2-Deoxokanshone M (64.23%) and 2-deoxokanshone L (1.10%)] and two known compounds [desoxo-narchinol A (2.17%) and isonardosinone (3.44%)], were firstly afforded from the refluxed products of nardosinone in boiling water; their structures were identified using an analysis of the extensive NMR and X-ray diffraction data and the simulation and comparison of electronic circular dichroism spectra. Compared with nardosinone, 2-Deoxokanshone M exhibited potent vasodilatory activity without any of the significant anti-neuroinflammatory activity that nardosinone contains. Secondly, UPLC-PDA and UHPLC-DAD/Q-TOF MS analyses on the degradation patterns of nardosinone revealed that nardosinone degraded more easily under high temperatures and in simulated gastric fluid compared with the simulated intestinal fluid. A plausible degradation pathway of nardosinone was finally proposed using nardosinonediol as the initial intermediate and involved multiple chemical reactions, including peroxy ring-opening, keto-enol tautomerization, oxidation, isopropyl cleavage, and pinacol rearrangement. Our findings may supply certain guidance and scientific evidence for the quality control and reasonable application of nardosinone-related products.

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