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Japonicone D
Japonicone D
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Japonicone D
Price:
CAS No.: 1078711-42-8
Catalog No.: CFN92708
Molecular Formula: C34H44O9
Molecular Weight: 596.7 g/mol
Purity: >=98%
Type of Compound: Triterpenoids
Physical Desc.: Powder
Source: The herbs of Inula japonica Thunb.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF
Similar structural: Comparison (Web)  (SDF)
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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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Product Use Citation
Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
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Description: Standard reference
Japonicone D Description
Source: The herbs of Inula japonica Thunb.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals
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Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.6759 mL 8.3794 mL 16.7588 mL 33.5177 mL 41.8971 mL
5 mM 0.3352 mL 1.6759 mL 3.3518 mL 6.7035 mL 8.3794 mL
10 mM 0.1676 mL 0.8379 mL 1.6759 mL 3.3518 mL 4.1897 mL
50 mM 0.0335 mL 0.1676 mL 0.3352 mL 0.6704 mL 0.8379 mL
100 mM 0.0168 mL 0.0838 mL 0.1676 mL 0.3352 mL 0.419 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Japonicone D References Information
Citation [1]

Bioorg Med Chem Lett. 2009 Feb 1;19(3):710-3.

Japonicones A-D, bioactive dimeric sesquiterpenes from Inula japonica Thunb.[Pubmed: 19117757]
Four new dimeric sesquiterpene lactones japonicone A, japonicone B, japonicone C, Japonicone D (1-4), comprised by eudesmane and guaiane sesquiterpenes, were isolated from the aerial part of Inula japonica Thunb. The structures and stereochemistry of 1-4 were elucidated by use of 2D NMR spectroscopic techniques, X-ray crystallography and modified Mosher method. Japonicone A (1) showed the most potent cytotoxicities against four tumor cell lines, A549, LOVO, CEM and MDA-MB-435.
CFN92708Japonicone D1078711-42-8596.7C34H44O9
CFN92801Inulanolide A888941-86-4596.7C34H44O9
CFN90168Absinthiin1362-42-1496.62C30H40O6
CFN90906Handelin62687-22-3552.7C32H40O8
CFN99048Pre-schisanartanin B1033288-92-4590.7 C31H42O11
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