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Cnidimol A
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Product Name Cnidimol A
Price:
CAS No.: 103629-80-7
Catalog No.: CFN96860
Molecular Formula: C15H16O5
Molecular Weight: 276.28 g/mol
Purity: >=98%
Type of Compound: Phenols
Physical Desc.: Powder
Source: The aerial parts of Cnidium monnieri.
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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10 mM * 1 mL in DMSO / Inquiry / In-stock
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Biological Activity
Description: Cnidimol A is a natural product from Cnidium monnieri.
Cnidimol A Description
Source: The aerial parts of Cnidium monnieri.
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

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 3.6195 mL 18.0976 mL 36.1952 mL 72.3903 mL 90.4879 mL
5 mM 0.7239 mL 3.6195 mL 7.239 mL 14.4781 mL 18.0976 mL
10 mM 0.362 mL 1.8098 mL 3.6195 mL 7.239 mL 9.0488 mL
50 mM 0.0724 mL 0.362 mL 0.7239 mL 1.4478 mL 1.8098 mL
100 mM 0.0362 mL 0.181 mL 0.362 mL 0.7239 mL 0.9049 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:
Phytochemistry, 1992, 31(4):1367-1370.
Chromones from Cnidium monnieri.[Reference: WebLink]
Four new chromones, cnidimol C–F, along with Cnidimol A, cnidimol B and karenin were isolated from the aerial parts of Cnidium monnieri.
METHODS AND RESULTS:
The structures of the new chromones were determined to be 5,7-dihydroxy-2-hydroxy-methylchromone, 5,7-dihydroxy-6-[(2Z)-3-hydroxymethyl-2-butenyl]-2-hydroxymethylchromone, 5,7-dihydroxy-6-[2-hydroxy-3-methyl-3-butenyl]- 2-hydroxymethylchromone and 5,8-dihydroxy-2-hydroxymethyl-8-methyl-4H,9H-pyrano [3,2-h][1]benzoxepin-4-one.
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Schaftoside

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