Kanshone H

CAS# 1445952-33-9

Kanshone H

Catalog No. BCN7627----Order now to get a substantial discount!

Product Name & Size Price Stock
Kanshone H: 5mg $811 In Stock
Kanshone H: 10mg Please Inquire In Stock
Kanshone H: 20mg Please Inquire Please Inquire
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Quality Control of Kanshone H

Number of papers citing our products

Chemical structure

Kanshone H

3D structure

Chemical Properties of Kanshone H

Cas No. 1445952-33-9 SDF Download SDF
PubChem ID 86293425 Appearance Powder
Formula C15H20O M.Wt 216.31
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (1aR,7R,7aR,7bS)-1,1,7,7a-tetramethyl-1a,6,7,7b-tetrahydrocyclopropa[a]naphthalen-2-one
SMILES CC1CC=CC2=CC(=O)C3C(C12C)C3(C)C
Standard InChIKey BVLHCTFFMIUHGN-JWFUOXDNSA-N
Standard InChI InChI=1S/C15H20O/c1-9-6-5-7-10-8-11(16)12-13(14(12,2)3)15(9,10)4/h5,7-9,12-13H,6H2,1-4H3/t9-,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 Kanshone H

The rhizomes and roots of Nardostachys chinensis.

Kanshone H Dilution Calculator

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Kanshone H Molarity Calculator

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Preparing Stock Solutions of Kanshone H

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.623 mL 23.115 mL 46.2299 mL 92.4599 mL 115.5749 mL
5 mM 0.9246 mL 4.623 mL 9.246 mL 18.492 mL 23.115 mL
10 mM 0.4623 mL 2.3115 mL 4.623 mL 9.246 mL 11.5575 mL
50 mM 0.0925 mL 0.4623 mL 0.9246 mL 1.8492 mL 2.3115 mL
100 mM 0.0462 mL 0.2311 mL 0.4623 mL 0.9246 mL 1.1557 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 Kanshone H

A Simple and Rapid UPLC-PDA Method for Quality Control of Nardostachys jatamansi.[Pubmed:29202512]

Planta Med. 2018 May;84(8):536-543.

Nardostachys jatamansi is a well-documented herbal agent used to treat digestive and neuropsychiatric disorders in oriental medicinal systems. However, few simple, rapid, and comprehensive methods were reported for quality assessment and control of N. jatamansi. Herein, a UPLC with photodiode array detection method was developed for both fingerprint investigation of N. jatamansi and simultaneous quantitative analysis of the six serotonin transporter modulatory constituents in N. jatamansi. For chromatographic fingerprinting, 24 common peaks were selected as characteristic peaks to assess the consistency of N. jatamansi samples from different retail sources. Six of the common peaks (5, 7, 12: , and 16: - 18: ) were identified as desoxo-narchinol A, buddleoside, isonardosinone, nardosinone, Kanshone H, and (-)-aristolone, respectively, by phytochemical investigation. Five of the six compounds significantly either enhanced or inhibited serotonin transporter activity, while (-)-aristolone (18: ) didn't show any serotonin transporter activity. In quantitative analysis, the six compounds showed good linearity (r > 0.999) within test ranges. The precision, expressed as relative standard deviation, was in the range of 0.25 - 2.77%, and the recovery of the method was in the range of 92 - 105%. The UPLC-photodiode array detection-based fingerprint analysis and quantitative methods reported here could be used for routine quality control of N. jatamansi.

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