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Diversoside
Diversoside
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Diversoside
Price: $318 / 10mg
CAS No.: 55062-36-7
Catalog No.: CFN89254
Molecular Formula: C25H34O10
Molecular Weight: 494.53 g/mol
Purity: >=98%
Type of Compound: Coumarins
Physical Desc.: Powder
Source: The aerial parts of Aster subspicatus.
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Download: COA    MSDS
Similar structural: Comparison
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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 / $206.7 / In-stock
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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
Biological Activity
Description: Diversoside is a natural product from Aster subspicatus.
Diversoside Description
Source: The aerial parts of Aster subspicatus.
Solvent: DMSO, Pyridine, Methanol, Ethanol, 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 2.0221 mL 10.1106 mL 20.2212 mL 40.4424 mL 50.5531 mL
5 mM 0.4044 mL 2.0221 mL 4.0442 mL 8.0885 mL 10.1106 mL
10 mM 0.2022 mL 1.0111 mL 2.0221 mL 4.0442 mL 5.0553 mL
50 mM 0.0404 mL 0.2022 mL 0.4044 mL 0.8088 mL 1.0111 mL
100 mM 0.0202 mL 0.1011 mL 0.2022 mL 0.4044 mL 0.5055 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.
Protocol
Structure Identification:
Pharmazie. 2002 Aug;57(8):567-9.
Terpenoid constituents of Aster subspicatus and A. ageratoides.[Pubmed: 12227200]

METHODS AND RESULTS:
Chemical investigation of the aerial parts of Aster subspicatus afforded a new sesquiterpene lactone, 8 alpha-acetoxy-1 alpha-hydroxy-3 alpha,4 alpha-epoxy-5 alpha,7 alpha H-9,11(13)-guaiadien-12,6 alpha-olide (1), in addition to the known compounds arteglasin-B (2), Diversoside (3), and 2-phenylethyl beta-D-glucopyranoside. Re-investigation of Aster ageratoides afforded the known compounds crotocorylifuran, and oplopanone.
CONCLUSIONS:
The structure of the new compound was determined by spectroscopic methods particularly high resolution 1H, 13C NMR, DEPT, 2D 1H-1H and 1H-13C COSY NMR and HMBC analysis.
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