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Ophiopogonanone F
Ophiopogonanone F
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Ophiopogonanone F
Price:
CAS No.: 588706-67-6
Catalog No.: CFN96338
Molecular Formula: C20H22O7
Molecular Weight: 374.4 g/mol
Purity: >=98%
Type of Compound: Flavonoids
Physical Desc.: Powder
Source: The tubers of Ophiopogon japonicus(Thunb) Ker-Gawl.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS
Similar structural: Comparison (Web)  (SDF)
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Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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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: Ophiopogonanone F can be used for preparing a drug for resisting hepatocellular injury.
In vitro:
CN 104257651 A[P]. 2015.
Medical application of ophiopogonanone F[Reference: WebLink]

METHODS AND RESULTS:
The invention relates to the field of medical health products and particularly relates to medical application and a product of Ophiopogonanone F. The Ophiopogonanone F disclosed by the invention can be used for preparing a drug for resisting hepatocellular injury.
Ophiopogonanone F Description
Source: The tubers of Ophiopogon japonicus(Thunb) Ker-Gawl.
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
More...

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 2.6709 mL 13.3547 mL 26.7094 mL 53.4188 mL 66.7735 mL
5 mM 0.5342 mL 2.6709 mL 5.3419 mL 10.6838 mL 13.3547 mL
10 mM 0.2671 mL 1.3355 mL 2.6709 mL 5.3419 mL 6.6774 mL
50 mM 0.0534 mL 0.2671 mL 0.5342 mL 1.0684 mL 1.3355 mL
100 mM 0.0267 mL 0.1335 mL 0.2671 mL 0.5342 mL 0.6677 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:
J Nat Prod. 2002 Nov;65(11):1731-3.
Five new homoisoflavonoids from the tuber of Ophiopogon japonicus.[Pubmed: 12444717]

METHODS AND RESULTS:
Five new homoisoflavonoids, ophiopogonanone C (1), ophiopogonanone D (2), ophiopogonone C (3), ophiopogonanone E (4) and Ophiopogonanone F (5), and six known compounds were isolated from an ethanol extract of the tubers of Ophiopogon japonicus (Thunb) Ker-Gawl. Spectroscopic analyses were used to elucidate the structures of these compounds.
CFN963395,7-Dihydroxy-3-(4-hydroxy-3,5-dimethoxybenzyl)-6,8-dimethylchroman-4-one212201-12-2374.4C20H22O7
CFN963366-Aldehydo-isoophiopogonone A112500-90-0354.3C19H14O7
CFN907316-Aldehydoisoophiopogonanone A116291-82-8356.33C19H16O7
CFN96327Ophiopogonanone C477336-75-7356.3C19H16O7
CFN92828Dihydrobonducellin103680-87-1284.3C17H16O4
CFN992293-Deoxysappanone B113122-54-6286.3 C16H14O5
CFN990824-Demethyl-3,9-dihydroeucomin107585-77-3286.3 C16H14O5
CFN965193,9-Dihydroeucomin887375-68-0300.31C17H16O5
CFN911444H-1-Benzopyran-4-one,2,3-dihydro-5-hydroxy-3-[(4-hydroxyphenyl)methyl]-7-methoxy-108001-32-7300.3C17H16O5
CFN91153Loureiriol479195-44-3302.3C16H14O6
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